Item | Value |
---|---|
geneid | 8975 |
ensemblid | ENSG00000058056.10 |
hgncid | 12611 |
symbol | USP13 |
name | ubiquitin specific peptidase 13 |
refseq_nuc | NM_003940.3 |
refseq_prot | NP_003931.2 |
ensembl_nuc | ENST00000263966.8 |
ensembl_prot | ENSP00000263966.3 |
mane_status | MANE Select |
chr | chr3 |
start | 179653040 |
end | 179789401 |
strand | + |
ver | v1.2 |
region | chr3:179653040-179789401 |
region5000 | chr3:179648040-179794401 |
regionname0 | USP13_chr3_179653040_179789401 |
regionname5000 | USP13_chr3_179648040_179794401 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 863 | 293 | 88 | 58 | 101 | 8 | 36 | 70 | USP13_chr3_179648040_179794401 | USP13 | MQRRG others(858): Show |
chr3 | 179648040 | 179794401 |
a0002 | 0/0 | 863 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | USP13_chr3_179648040_179794401 | USP13 | MQRRG others(858): Show |
chr3 | 179648040 | 179794401 |
a0003 | 0/0 | 863 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | USP13_chr3_179648040_179794401 | USP13 | MQRRG others(858): Show |
chr3 | 179648040 | 179794401 |
a0004 | 0/0 | 863 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | MQRRG others(858): Show |
chr3 | 179648040 | 179794401 |
a0005 | 0/0 | 863 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | MQRRG others(858): Show |
chr3 | 179648040 | 179794401 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2589 | 205 | 45 | 40 | 87 | 6 | 25 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0002 | 0/0 | 2589 | 55 | 20 | 14 | 14 | 1 | 6 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0003 | 0/0 | 2589 | 7 | 6 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0004 | 0/0 | 2589 | 6 | 1 | 1 | 0 | 1 | 3 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0005 | 0/0 | 2589 | 6 | 5 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0006 | 0/0 | 2589 | 5 | 3 | 0 | 0 | 0 | 2 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0008 | 0/0 | 2589 | 3 | 2 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0009 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0011 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0012 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0015 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0001c0016 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0002c0007 | 0/0 | 2589 | 3 | 0 | 0 | 3 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0003c0010 | 0/0 | 2589 | 2 | 0 | 0 | 0 | 0 | 2 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0004c0013 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 | ||
a0005c0014 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | ATGCA others(2584): Show |
chr3 | 179648040 | 179794401 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 8038 | 83 | 8 | 19 | 42 | 1 | 11 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0002 | 0/0 | 8035 | 35 | 0 | 4 | 23 | 4 | 4 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0003 | 0/0 | 8038 | 20 | 3 | 6 | 11 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0004 | 0/0 | 8038 | 7 | 5 | 2 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0005 | 0/0 | 8038 | 7 | 7 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0006 | 0/0 | 8039 | 9 | 3 | 3 | 0 | 0 | 3 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8034): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0007 | 0/0 | 8035 | 6 | 2 | 3 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0008 | 0/0 | 8038 | 3 | 1 | 1 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0009 | 0/0 | 8039 | 2 | 0 | 0 | 0 | 0 | 2 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8034): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0010 | 0/0 | 8035 | 5 | 4 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0011 | 0/0 | 8038 | 4 | 0 | 0 | 4 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0012 | 0/0 | 8038 | 2 | 0 | 0 | 0 | 0 | 2 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0013 | 0/0 | 8040 | 2 | 0 | 0 | 0 | 0 | 2 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8035): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0014 | 0/0 | 8038 | 2 | 2 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0015 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0017 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0018 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0019 | 0/0 | 8039 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8034): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0020 | 0/0 | 8035 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0021 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0022 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0023 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0024 | 0/0 | 8038 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0026 | 0/0 | 8038 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0027 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0028 | 0/0 | 8038 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0030 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0031 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0035 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8031): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0036 | 0/0 | 8035 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0037 | 0/0 | 8035 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0001t0038 | 0/0 | 8038 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0001 | 0/0 | 8038 | 19 | 4 | 6 | 5 | 1 | 3 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0002 | 0/0 | 8035 | 4 | 0 | 1 | 2 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0003 | 0/0 | 8038 | 5 | 3 | 0 | 2 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0004 | 0/0 | 8038 | 6 | 6 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0005 | 0/0 | 8038 | 2 | 2 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0006 | 0/0 | 8039 | 2 | 1 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8034): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0007 | 0/0 | 8035 | 5 | 1 | 3 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0008 | 0/0 | 8038 | 2 | 0 | 2 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0009 | 0/0 | 8039 | 2 | 0 | 1 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8034): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0015 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0016 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0029 | 0/0 | 8038 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0033 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0040 | 0/0 | 8038 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0041 | 0/0 | 8035 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0042 | 0/0 | 8038 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0002t0043 | 0/0 | 8038 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0003t0001 | 0/0 | 8038 | 4 | 3 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0003t0005 | 0/0 | 8038 | 2 | 2 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0003t0039 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0004t0002 | 0/0 | 8035 | 2 | 0 | 0 | 0 | 0 | 2 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0004t0006 | 0/0 | 8039 | 2 | 0 | 1 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8034): Show |
chr3 | 179648040 | 179794401 |
a0001c0004t0012 | 0/0 | 8038 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0004t0034 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0005t0001 | 0/0 | 8038 | 4 | 3 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0005t0005 | 0/0 | 8038 | 2 | 2 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0006t0001 | 0/0 | 8038 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0006t0002 | 0/0 | 8035 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8030): Show |
chr3 | 179648040 | 179794401 |
a0001c0006t0004 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0006t0006 | 0/0 | 8039 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8034): Show |
chr3 | 179648040 | 179794401 |
a0001c0006t0032 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0008t0004 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0008t0008 | 0/0 | 8038 | 2 | 1 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0009t0005 | 0/0 | 8038 | 2 | 2 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0011t0025 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0012t0004 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0015t0008 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0001c0016t0004 | 0/0 | 8038 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0002c0007t0001 | 0/0 | 8038 | 3 | 0 | 0 | 3 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0003c0010t0009 | 0/0 | 8039 | 2 | 0 | 0 | 0 | 0 | 2 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8034): Show |
chr3 | 179648040 | 179794401 |
a0004c0013t0001 | 0/0 | 8038 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
a0005c0014t0001 | 0/0 | 8038 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | AGTCC others(8033): Show |
chr3 | 179648040 | 179794401 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0006g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0008g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0009g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0009g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0010g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0011g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0012g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0012g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0013g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0013g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0014g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0015g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0017g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0018g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0019g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0020g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0021g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0022g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0023g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0024g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0026g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0027g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0028g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0030g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0031g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0035g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0036g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0037g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0001t0038g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0007g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0007g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0008g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0008g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0009g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0009g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0016g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0029g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0033g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0040g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0041g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0042g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0002t0043g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0003t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0003t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0003t0039g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0004t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0004t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0004t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0004t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0004t0012g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0004t0034g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0005t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0005t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0005t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0005t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0005t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0006t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0006t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0006t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0006t0032g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0008t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0008t0008g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0008t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0009t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0009t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0011t0025g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0012t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0015t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0001c0016t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0002c0007t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0002c0007t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0002c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0003c0010t0009g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0003c0010t0009g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0004c0013t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
a0005c0014t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | GBR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00140 | hp2 | a0001 | c0004 | t0006 | g0226 | EUR | GBR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | FIN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0137 | EUR | FIN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0097 | EUR | FIN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00323 | hp2 | a0001 | c0001 | t0007 | g0099 | EUR | FIN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00735 | hp1 | a0001 | c0001 | t0024 | g0235 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00738 | hp2 | a0001 | c0001 | t0007 | g0106 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0273 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG00741 | hp2 | a0001 | c0001 | t0007 | g0013 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01069 | hp2 | a0001 | c0002 | t0007 | g0175 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01070 | hp1 | a0001 | c0002 | t0008 | g0165 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01071 | hp1 | a0001 | c0002 | t0007 | g0001 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01071 | hp2 | a0001 | c0002 | t0008 | g0164 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01081 | hp1 | a0001 | c0002 | t0009 | g0160 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0234 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01099 | hp1 | a0001 | c0004 | t0006 | g0107 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0297 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01109 | hp2 | a0001 | c0008 | t0008 | g0237 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0293 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01175 | hp2 | a0001 | c0002 | t0007 | g0168 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PUR | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01255 | hp2 | a0001 | c0005 | t0001 | g0151 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0035 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01258 | hp2 | a0001 | c0002 | t0006 | g0157 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01361 | hp1 | a0001 | c0001 | t0007 | g0209 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0230 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01884 | hp1 | a0001 | c0001 | t0031 | g0227 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01884 | hp2 | a0001 | c0002 | t0005 | g0136 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01891 | hp1 | a0001 | c0009 | t0005 | g0238 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01978 | hp1 | a0001 | c0001 | t0010 | g0195 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0239 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02080 | hp1 | a0001 | c0001 | t0020 | g0059 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02145 | hp1 | a0001 | c0011 | t0025 | g0183 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02145 | hp2 | a0001 | c0012 | t0004 | g0289 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CDX | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | CDX | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02257 | hp1 | a0001 | c0009 | t0005 | g0291 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02257 | hp2 | a0001 | c0002 | t0015 | g0130 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02258 | hp1 | a0001 | c0001 | t0010 | g0193 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02280 | hp1 | a0001 | c0002 | t0004 | g0172 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02572 | hp1 | a0001 | c0002 | t0005 | g0171 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0240 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0073 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02615 | hp1 | a0001 | c0008 | t0004 | g0264 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02615 | hp2 | a0001 | c0001 | t0018 | g0191 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02622 | hp1 | a0001 | c0015 | t0008 | g0133 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02622 | hp2 | a0001 | c0003 | t0005 | g0002 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02630 | hp1 | a0001 | c0002 | t0004 | g0270 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02630 | hp2 | a0001 | c0002 | t0004 | g0143 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02647 | hp1 | a0001 | c0002 | t0016 | g0173 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0176 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02683 | hp1 | a0001 | c0001 | t0009 | g0101 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02683 | hp2 | a0001 | c0004 | t0002 | g0267 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02698 | hp1 | a0001 | c0004 | t0012 | g0062 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0116 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0292 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02723 | hp1 | a0001 | c0001 | t0010 | g0194 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0198 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02738 | hp1 | a0001 | c0001 | t0008 | g0040 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02809 | hp2 | a0001 | c0005 | t0001 | g0142 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02818 | hp1 | a0001 | c0003 | t0039 | g0019 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02818 | hp2 | a0001 | c0001 | t0017 | g0192 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02886 | hp1 | a0001 | c0005 | t0005 | g0178 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02886 | hp2 | a0001 | c0001 | t0022 | g0257 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02896 | hp1 | a0001 | c0008 | t0008 | g0265 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0288 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02965 | hp2 | a0001 | c0005 | t0005 | g0122 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02976 | hp1 | a0001 | c0002 | t0007 | g0001 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02976 | hp2 | a0001 | c0002 | t0033 | g0174 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03017 | hp1 | a0001 | c0001 | t0012 | g0113 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0263 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03130 | hp1 | a0001 | c0001 | t0014 | g0276 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0196 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03139 | hp2 | a0001 | c0002 | t0004 | g0186 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03195 | hp1 | a0001 | c0006 | t0032 | g0140 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0241 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03225 | hp2 | a0001 | c0006 | t0004 | g0179 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03239 | hp2 | a0001 | c0001 | t0012 | g0070 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03453 | hp1 | a0001 | c0002 | t0006 | g0169 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03453 | hp2 | a0001 | c0005 | t0001 | g0188 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0268 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03490 | hp1 | a0001 | c0001 | t0009 | g0103 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03490 | hp2 | a0003 | c0010 | t0009 | g0102 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03516 | hp1 | a0001 | c0005 | t0001 | g0150 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03516 | hp2 | a0001 | c0004 | t0034 | g0072 | AFR | ESN | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03540 | hp1 | a0001 | c0002 | t0004 | g0187 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03579 | hp2 | a0001 | c0001 | t0023 | g0262 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03669 | hp2 | a0001 | c0002 | t0009 | g0141 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0154 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03834 | hp1 | a0001 | c0001 | t0013 | g0023 | SAS | BEB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0159 | SAS | BEB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0228 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04184 | hp1 | a0001 | c0004 | t0002 | g0182 | SAS | BEB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04199 | hp1 | a0001 | c0006 | t0002 | g0138 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0149 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04204 | hp2 | a0003 | c0010 | t0009 | g0069 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04228 | hp1 | a0001 | c0001 | t0013 | g0015 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG04228 | hp2 | a0001 | c0006 | t0001 | g0153 | SAS | STU | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18522 | hp1 | a0001 | c0016 | t0004 | g0189 | AFR | YRI | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18522 | hp2 | a0001 | c0006 | t0006 | g0181 | AFR | YRI | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18612 | hp1 | a0001 | c0001 | t0011 | g0224 | EAS | CHB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18612 | hp2 | a0004 | c0013 | t0001 | g0010 | EAS | CHB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18941 | hp1 | a0001 | c0001 | t0036 | g0285 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18947 | hp2 | a0002 | c0007 | t0001 | g0243 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18949 | hp1 | a0001 | c0002 | t0029 | g0128 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18949 | hp2 | a0001 | c0002 | t0041 | g0124 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18950 | hp1 | a0002 | c0007 | t0001 | g0253 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18954 | hp1 | a0005 | c0014 | t0001 | g0076 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18966 | hp2 | a0001 | c0002 | t0043 | g0125 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18967 | hp1 | a0001 | c0001 | t0035 | g0056 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18967 | hp2 | a0001 | c0002 | t0003 | g0123 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18977 | hp2 | a0001 | c0002 | t0040 | g0126 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18992 | hp2 | a0001 | c0002 | t0042 | g0129 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18994 | hp2 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19000 | hp2 | a0001 | c0001 | t0037 | g0029 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19005 | hp2 | a0001 | c0001 | t0011 | g0065 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | LWK | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19030 | hp2 | a0001 | c0001 | t0014 | g0184 | AFR | LWK | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19043 | hp1 | a0001 | c0001 | t0030 | g0258 | AFR | LWK | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0290 | AFR | LWK | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19055 | hp1 | a0001 | c0001 | t0011 | g0057 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19060 | hp1 | a0001 | c0001 | t0026 | g0049 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19065 | hp2 | a0001 | c0001 | t0028 | g0033 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19077 | hp2 | a0001 | c0001 | t0038 | g0008 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19081 | hp1 | a0001 | c0001 | t0011 | g0252 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19090 | hp1 | a0002 | c0007 | t0001 | g0200 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | YRI | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | YRI | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0158 | AFR | ASW | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA20129 | hp2 | a0001 | c0001 | t0021 | g0295 | AFR | ASW | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | GIH | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA20905 | hp2 | a0001 | c0002 | t0007 | g0166 | SAS | GIH | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02109 | hp1 | a0001 | c0001 | t0010 | g0197 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02486 | hp2 | a0001 | c0002 | t0003 | g0180 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02559 | hp1 | a0001 | c0003 | t0005 | g0242 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0255 | AFR | ACB | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03471 | hp1 | a0001 | c0001 | t0027 | g0199 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG03471 | hp2 | a0001 | c0002 | t0004 | g0170 | AFR | MSL | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
HG06807 | hp2 | a0001 | c0001 | t0019 | g0204 | AFR | USA | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0233 | AFR | USA | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | USA | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | LWK | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0269 | REF | REF | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0271 | REF | REF | USP13_chr3_179648040_179794401 | USP13 | chr3 | 179648040 | 179794401 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179690266 | C | T | 1 | a0003 | 2 | HG03490.hp2 HG04204.hp2 |
missense_variant | MODERATE | c.320C>T | p.Ala107Val | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/21 | 506/8038 | 320/2592 | 107/863 | chr3 | 179690266 | |||
chr3:179690298 | T | A | 1 | a0002 | 3 | NA18947.hp2 NA18950.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.352T>A | p.Leu118Ile | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/21 | 538/8038 | 352/2592 | 118/863 | chr3 | 179690298 | |||
chr3:179720000 | C | T | 1 | a0005 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.866C>T | p.Ala289Val | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/21 | 1052/8038 | 866/2592 | 289/863 | chr3 | 179720000 | |||
chr3:179721414 | C | T | 1 | a0004 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.913C>T | p.Leu305Phe | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/21 | 1099/8038 | 913/2592 | 305/863 | chr3 | 179721414 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179653366 | C | T | 5 | a0001c0002 a0001c0005 a0001c0006 others(2): Show |
68 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(65): Show |
synonymous_variant | LOW | c.141C>T | p.Asn47Asn | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/21 | 327/8038 | 141/2592 | 47/863 | chr3 | 179653366 | |||
chr3:179707074 | A | G | 2 | a0001c0004 a0001c0006 |
11 | HG00140.hp2 HG01099.hp1 HG02683.hp2 others(8): Show |
splice_region_variant&synonymous_variant | LOW | c.618A>G | p.Pro206Pro | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/21 | 804/8038 | 618/2592 | 206/863 | chr3 | 179707074 | |||
chr3:179708794 | C | T | 2 | a0001c0009 a0001c0016 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.642C>T | p.Cys214Cys | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/21 | 828/8038 | 642/2592 | 214/863 | chr3 | 179708794 | |||
chr3:179721512 | T | A | 1 | a0001c0011 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1011T>A | p.Gly337Gly | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/21 | 1197/8038 | 1011/2592 | 337/863 | chr3 | 179721512 | |||
chr3:179740366 | A | G | 1 | a0001c0012 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1374A>G | p.Leu458Leu | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/21 | 1560/8038 | 1374/2592 | 458/863 | chr3 | 179740366 | |||
chr3:179742292 | G | A | 2 | a0001c0008 a0001c0015 |
4 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
synonymous_variant | LOW | c.1476G>A | p.Thr492Thr | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/21 | 1662/8038 | 1476/2592 | 492/863 | chr3 | 179742292 | |||
chr3:179754826 | C | G | 3 | a0001c0003 a0001c0005 a0001c0009 |
15 | HG01255.hp2 HG01433.hp1 HG01891.hp1 others(12): Show |
synonymous_variant | LOW | c.1893C>G | p.Pro631Pro | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/21 | 2079/8038 | 1893/2592 | 631/863 | chr3 | 179754826 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179653124 | G | C | 1 | a0001c0002t0016 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-102G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/21 | 102 | chr3 | 179653124 | ||||||
chr3:179653133 | G | T | 4 | a0001c0002t0040 a0001c0002t0041 a0001c0002t0042 others(1): Show |
4 | NA18949.hp2 NA18966.hp2 NA18977.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-93G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/21 | 93 | chr3 | 179653133 | ||||||
chr3:179653148 | C | G | 1 | a0001c0002t0043 | 1 | NA18966.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-78C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/21 | chr3 | 179653148 | |||||||
chr3:179653207 | T | C | 3 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0018 |
7 | HG01978.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-19T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/21 | 19 | chr3 | 179653207 | ||||||
chr3:179784193 | C | CA | 6 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0019 others(3): Show |
17 | HG00140.hp2 HG00741.hp1 HG01099.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*63dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 64 | INFO_REALIGN_3_PRIME | chr3 | 179784193 | |||||
chr3:179784218 | T | C | 2 | a0001c0001t0003 a0001c0002t0003 |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*77T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 77 | chr3 | 179784218 | ||||||
chr3:179784291 | T | C | 1 | a0001c0001t0020 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 150 | chr3 | 179784291 | ||||||
chr3:179784438 | A | C | 6 | a0001c0001t0005 a0001c0001t0018 a0001c0002t0005 others(3): Show |
16 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*297A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 297 | chr3 | 179784438 | ||||||
chr3:179784892 | A | G | 1 | a0001c0003t0039 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*751A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 751 | chr3 | 179784892 | ||||||
chr3:179784908 | A | G | 1 | a0001c0001t0038 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 767 | chr3 | 179784908 | ||||||
chr3:179784909 | G | A | 1 | a0001c0001t0021 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 768 | chr3 | 179784909 | ||||||
chr3:179784948 | T | A | 4 | a0001c0001t0006 a0001c0002t0006 a0001c0004t0006 others(1): Show |
14 | HG00140.hp2 HG00741.hp1 HG01099.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*807T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 807 | chr3 | 179784948 | ||||||
chr3:179784953 | C | G | 1 | a0001c0001t0037 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*812C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 812 | chr3 | 179784953 | ||||||
chr3:179785219 | G | A | 1 | a0001c0001t0022 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1078G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 1078 | chr3 | 179785219 | ||||||
chr3:179785434 | G | C | 2 | a0001c0001t0014 a0001c0001t0023 |
3 | HG03130.hp1 HG03579.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1293G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 1293 | chr3 | 179785434 | ||||||
chr3:179785501 | G | A | 4 | a0001c0001t0008 a0001c0002t0008 a0001c0008t0008 others(1): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1360G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 1360 | chr3 | 179785501 | ||||||
chr3:179785531 | A | G | 2 | a0001c0001t0011 a0001c0002t0042 |
5 | NA18612.hp1 NA18992.hp2 NA19005.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1390A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 1390 | chr3 | 179785531 | ||||||
chr3:179785553 | G | A | 1 | a0001c0001t0024 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1412G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 1412 | chr3 | 179785553 | ||||||
chr3:179786042 | CAGA | C | 14 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(11): Show |
65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1904_*1906delAAG | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 1904 | INFO_REALIGN_3_PRIME | chr3 | 179786042 | |||||
chr3:179786249 | C | T | 2 | a0001c0001t0003 a0001c0002t0003 |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2108C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2108 | chr3 | 179786249 | ||||||
chr3:179786437 | A | G | 15 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(12): Show |
66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2296A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2296 | chr3 | 179786437 | ||||||
chr3:179786458 | T | C | 1 | a0001c0011t0025 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2317T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2317 | chr3 | 179786458 | ||||||
chr3:179786521 | C | T | 21 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(18): Show |
75 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2380C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2380 | chr3 | 179786521 | ||||||
chr3:179786755 | A | T | 1 | a0001c0001t0036 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2614A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2614 | chr3 | 179786755 | ||||||
chr3:179786757 | G | A | 15 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(12): Show |
66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2616G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2616 | chr3 | 179786757 | ||||||
chr3:179786910 | T | A | 2 | a0001c0001t0003 a0001c0002t0003 |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2769T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2769 | chr3 | 179786910 | ||||||
chr3:179786985 | C | T | 1 | a0001c0004t0034 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2844C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2844 | chr3 | 179786985 | ||||||
chr3:179786987 | A | G | 1 | a0001c0004t0034 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2846A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2846 | chr3 | 179786987 | ||||||
chr3:179786992 | G | C | 1 | a0001c0004t0034 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2851G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2851 | chr3 | 179786992 | ||||||
chr3:179787103 | A | G | 2 | a0001c0001t0003 a0001c0002t0003 |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2962A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2962 | chr3 | 179787103 | ||||||
chr3:179787131 | T | C | 1 | a0001c0001t0037 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2990T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 2990 | chr3 | 179787131 | ||||||
chr3:179787309 | G | A | 1 | a0001c0001t0023 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3168G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3168 | chr3 | 179787309 | ||||||
chr3:179787439 | G | A | 1 | a0001c0001t0026 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3298G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3298 | chr3 | 179787439 | ||||||
chr3:179787456 | T | G | 2 | a0001c0002t0016 a0001c0002t0033 |
2 | HG02647.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3315T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3315 | chr3 | 179787456 | ||||||
chr3:179787654 | G | T | 1 | a0001c0006t0032 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3513G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3513 | chr3 | 179787654 | ||||||
chr3:179787718 | C | T | 3 | a0001c0001t0007 a0001c0001t0010 a0001c0002t0007 |
16 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3577C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3577 | chr3 | 179787718 | ||||||
chr3:179787737 | G | A | 1 | a0001c0001t0027 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3596G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3596 | chr3 | 179787737 | ||||||
chr3:179787750 | C | T | 1 | a0001c0006t0032 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3609C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3609 | chr3 | 179787750 | ||||||
chr3:179787767 | A | G | 2 | a0001c0001t0012 a0001c0004t0012 |
3 | HG02698.hp1 HG03017.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3626A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3626 | chr3 | 179787767 | ||||||
chr3:179787807 | G | T | 1 | a0001c0001t0031 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3666G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3666 | chr3 | 179787807 | ||||||
chr3:179788076 | A | G | 19 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(16): Show |
50 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*3935A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 3935 | chr3 | 179788076 | ||||||
chr3:179788148 | G | A | 1 | a0001c0001t0028 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4007G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 4007 | chr3 | 179788148 | ||||||
chr3:179788219 | G | C | 1 | a0001c0002t0029 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4078G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 4078 | chr3 | 179788219 | ||||||
chr3:179788317 | G | C | 1 | a0001c0001t0022 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4176G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 4176 | chr3 | 179788317 | ||||||
chr3:179788613 | A | G | 1 | a0001c0001t0030 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4472A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 4472 | chr3 | 179788613 | ||||||
chr3:179788694 | A | G | 21 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(18): Show |
75 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*4553A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 4553 | chr3 | 179788694 | ||||||
chr3:179788894 | A | AT | 5 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0035 others(2): Show |
9 | HG01081.hp1 HG02683.hp1 HG03490.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4763dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 4764 | INFO_REALIGN_3_PRIME | chr3 | 179788894 | |||||
chr3:179788907 | G | T | 2 | a0001c0001t0035 a0001c0002t0041 |
2 | NA18949.hp2 NA18967.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4766G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 4766 | chr3 | 179788907 | ||||||
chr3:179788912 | A | G | 2 | a0001c0001t0015 a0001c0002t0015 |
2 | HG02257.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4771A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 4771 | chr3 | 179788912 | ||||||
chr3:179788933 | G | C | 14 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(11): Show |
65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*4792G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 21/21 | 4792 | chr3 | 179788933 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179653453 | G | T | 3 | a0001c0001t0003g0299 a0001c0001t0005g0298 a0001c0001t0006g0297 |
3 | HG01109.hp1 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+60G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653453 | |||||||
chr3:179653524 | T | C | 1 | a0001c0003t0005g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168+131T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653524 | |||||||
chr3:179653541 | T | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0002g0003 others(13): Show |
16 | HG00741.hp2 HG01433.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+148T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653541 | |||||||
chr3:179653544 | G | C | 103 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0027 others(100): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.168+151G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653544 | |||||||
chr3:179653628 | G | A | 56 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0134 others(53): Show |
57 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.168+235G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653628 | |||||||
chr3:179653661 | G | T | 1 | a0001c0001t0001g0121 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.168+268G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653661 | |||||||
chr3:179653695 | T | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0002g0003 others(76): Show |
80 | HG00280.hp2 HG00741.hp2 HG01069.hp1 others(77): Show |
intron_variant | MODIFIER | c.168+302T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653695 | |||||||
chr3:179653713 | G | C | 1 | a0001c0005t0005g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.168+320G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653713 | |||||||
chr3:179653753 | A | G | 103 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0027 others(100): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.168+360A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653753 | |||||||
chr3:179653820 | T | C | 2 | a0001c0001t0014g0184 a0001c0011t0025g0183 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.168+427T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653820 | |||||||
chr3:179653823 | G | A | 1 | a0001c0002t0003g0123 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.168+430G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653823 | |||||||
chr3:179653878 | A | G | 3 | a0001c0001t0003g0294 a0001c0001t0003g0296 a0001c0001t0021g0295 |
3 | HG02717.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+485A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653878 | |||||||
chr3:179653951 | A | G | 1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.168+558A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179653951 | |||||||
chr3:179654002 | G | A | 56 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0134 others(53): Show |
57 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.168+609G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654002 | |||||||
chr3:179654013 | C | T | 1 | a0001c0002t0003g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.168+620C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654013 | |||||||
chr3:179654213 | C | CA | 97 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0203 others(94): Show |
97 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.168+839dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179654213 | ||||||
chr3:179654213 | C | CAA | 73 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(70): Show |
74 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.168+838_168+839dup others(2): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179654213 | ||||||
chr3:179654213 | C | CAAA | 87 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(84): Show |
87 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.168+837_168+839dup others(3): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179654213 | ||||||
chr3:179654213 | C | CAAAA | 16 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0027 others(13): Show |
16 | HG01255.hp1 HG01258.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+836_168+839dup others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179654213 | ||||||
chr3:179654240 | C | A | 4 | a0001c0002t0004g0172 a0001c0002t0015g0130 a0001c0002t0016g0173 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+847C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654240 | |||||||
chr3:179654598 | C | T | 2 | a0001c0001t0004g0018 a0001c0001t0005g0017 |
2 | HG01433.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.168+1205C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654598 | |||||||
chr3:179654611 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.168+1218T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654611 | |||||||
chr3:179654635 | A | G | 1 | a0001c0003t0039g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.168+1242A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654635 | |||||||
chr3:179654742 | C | T | 3 | a0001c0001t0015g0292 a0001c0003t0001g0290 a0001c0009t0005g0291 |
3 | HG02257.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+1349C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654742 | |||||||
chr3:179654845 | G | C | 3 | a0001c0001t0001g0205 a0001c0001t0004g0206 a0001c0001t0019g0204 |
3 | HG06807.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.168+1452G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654845 | |||||||
chr3:179654849 | C | A | 28 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0211 others(25): Show |
28 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.168+1456C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654849 | |||||||
chr3:179654932 | A | G | 7 | a0001c0001t0010g0193 a0001c0001t0010g0194 a0001c0001t0010g0195 others(4): Show |
7 | HG01978.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+1539A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654932 | |||||||
chr3:179654933 | C | CT | 55 | a0001c0001t0001g0201 a0001c0001t0001g0205 a0001c0001t0001g0229 others(52): Show |
55 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.168+1549dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179654933 | ||||||
chr3:179654933 | C | CTT | 12 | a0001c0001t0001g0203 a0001c0001t0003g0299 a0001c0001t0004g0261 others(9): Show |
12 | HG02109.hp2 HG02615.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+1548_168+1549d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179654933 | ||||||
chr3:179654935 | T | C | 2 | a0001c0002t0001g0131 a0001c0002t0001g0132 |
2 | HG02165.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.168+1542T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179654935 | |||||||
chr3:179655012 | A | G | 63 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0205 others(60): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.168+1619A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655012 | |||||||
chr3:179655082 | A | C | 3 | a0001c0001t0015g0292 a0001c0003t0001g0290 a0001c0009t0005g0291 |
3 | HG02257.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+1689A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655082 | |||||||
chr3:179655094 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.168+1701G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655094 | |||||||
chr3:179655096 | C | CCTAA | 280 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(277): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.168+1706_168+1709d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655096 | ||||||
chr3:179655198 | A | C | 28 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0211 others(25): Show |
28 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.168+1805A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655198 | |||||||
chr3:179655231 | T | G | 2 | a0001c0001t0001g0287 a0001c0001t0031g0227 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.168+1838T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655231 | |||||||
chr3:179655456 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.168+2063A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655456 | |||||||
chr3:179655548 | G | GT | 95 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0027 others(92): Show |
95 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.168+2163dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655548 | ||||||
chr3:179655548 | G | GTTTT | 7 | a0001c0001t0004g0236 a0001c0001t0006g0288 a0001c0001t0008g0198 others(4): Show |
7 | HG00735.hp1 HG01109.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+2160_168+2163d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655548 | ||||||
chr3:179655548 | G | GTTTTT | 7 | a0001c0001t0001g0287 a0001c0001t0003g0294 a0001c0001t0003g0296 others(4): Show |
7 | HG02055.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+2159_168+2163d others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655548 | ||||||
chr3:179655548 | G | GTTTTTTT | 6 | a0001c0001t0003g0299 a0001c0001t0004g0261 a0001c0001t0005g0202 others(3): Show |
6 | HG02559.hp1 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+2157_168+2163d others(9): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655548 | ||||||
chr3:179655548 | G | GTTTTTTT others(1): Show |
14 | a0001c0001t0001g0203 a0001c0001t0001g0245 a0001c0001t0001g0246 others(11): Show |
14 | HG01884.hp1 HG02040.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+2156_168+2163d others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655548 | ||||||
chr3:179655548 | G | GTTTTTTT others(2): Show |
10 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(7): Show |
10 | HG01109.hp1 HG02027.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.168+2163_168+2164i others(11): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655548 | ||||||
chr3:179655548 | G | GTTTTTTT others(3): Show |
6 | a0001c0001t0001g0201 a0001c0001t0002g0117 a0001c0001t0003g0118 others(3): Show |
6 | HG00438.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+2163_168+2164i others(12): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655548 | ||||||
chr3:179655548 | G | GTTTTTTT others(4): Show |
2 | a0001c0001t0001g0259 a0001c0001t0002g0119 |
2 | HG00438.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.168+2163_168+2164i others(13): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655548 | ||||||
chr3:179655548 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0002g0120 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.168+2163_168+2164i others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655548 | ||||||
chr3:179655552 | TTTTTGTT others(3): Show |
T | 2 | a0001c0001t0001g0260 a0001c0001t0030g0258 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.168+2169_168+2178d others(12): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655552 | ||||||
chr3:179655555 | TTGTTTTG others(5): Show |
T | 2 | a0001c0001t0001g0229 a0001c0001t0006g0228 |
2 | HG01361.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.168+2164_168+2175d others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179655555 | ||||||
chr3:179655556 | TG | T | 27 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0211 others(24): Show |
27 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.168+2164delG | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655556 | |||||||
chr3:179655557 | G | T | 157 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0030 others(154): Show |
158 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.168+2164G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655557 | |||||||
chr3:179655558 | T | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0030 others(89): Show |
93 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.168+2165T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655558 | |||||||
chr3:179655561 | T | G | 91 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0027 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.168+2168T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655561 | |||||||
chr3:179655562 | G | T | 152 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0027 others(149): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.168+2169G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655562 | |||||||
chr3:179655565 | T | TG | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
5 | HG00558.hp1 HG00558.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+2172_168+2173i others(3): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655565 | |||||||
chr3:179655566 | T | G | 56 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0134 others(53): Show |
57 | HG00280.hp2 HG01069.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.168+2173T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655566 | |||||||
chr3:179655567 | G | T | 278 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(275): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.168+2174G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655567 | |||||||
chr3:179655568 | T | G | 29 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0211 others(26): Show |
29 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.168+2175T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655568 | |||||||
chr3:179655569 | T | G | 3 | a0001c0001t0015g0292 a0001c0003t0001g0290 a0001c0009t0005g0291 |
3 | HG02257.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+2176T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655569 | |||||||
chr3:179655570 | T | G | 1 | a0001c0015t0008g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.168+2177T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179655570 | |||||||
chr3:179656010 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0031g0227 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.168+2617C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179656010 | |||||||
chr3:179656070 | T | C | 1 | a0001c0002t0001g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.168+2677T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179656070 | |||||||
chr3:179656075 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.168+2682T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179656075 | |||||||
chr3:179656169 | G | A | 4 | a0001c0001t0001g0020 a0001c0002t0001g0134 a0001c0002t0001g0135 others(1): Show |
4 | HG01069.hp1 HG01884.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+2776G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179656169 | |||||||
chr3:179656291 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.168+2898A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179656291 | |||||||
chr3:179656547 | G | A | 28 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0001c0001t0001g0211 others(25): Show |
28 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.168+3154G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179656547 | |||||||
chr3:179656598 | C | T | 3 | a0001c0001t0015g0292 a0001c0003t0001g0290 a0001c0009t0005g0291 |
3 | HG02257.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+3205C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179656598 | |||||||
chr3:179656657 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.168+3264C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179656657 | |||||||
chr3:179656781 | C | T | 5 | a0001c0002t0004g0186 a0001c0002t0004g0187 a0001c0002t0004g0270 others(2): Show |
5 | HG02630.hp1 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+3388C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179656781 | |||||||
chr3:179657069 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.168+3676C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657069 | |||||||
chr3:179657073 | A | G | 1 | a0001c0001t0003g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.168+3680A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657073 | |||||||
chr3:179657172 | A | C | 1 | a0001c0001t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168+3779A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657172 | |||||||
chr3:179657255 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.168+3862C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657255 | |||||||
chr3:179657298 | A | T | 56 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0134 others(53): Show |
57 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.168+3905A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657298 | |||||||
chr3:179657484 | C | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0203 others(44): Show |
47 | HG00741.hp2 HG01109.hp1 HG01433.hp2 others(44): Show |
intron_variant | MODIFIER | c.168+4091C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657484 | |||||||
chr3:179657516 | A | G | 3 | a0001c0001t0015g0292 a0001c0003t0001g0290 a0001c0009t0005g0291 |
3 | HG02257.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+4123A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657516 | |||||||
chr3:179657533 | T | C | 278 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(275): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.168+4140T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657533 | |||||||
chr3:179657543 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0004g0206 a0001c0001t0019g0204 |
3 | HG06807.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.168+4150A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657543 | |||||||
chr3:179657558 | C | T | 56 | a0001c0001t0001g0205 a0001c0001t0004g0206 a0001c0001t0004g0234 others(53): Show |
57 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.168+4165C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657558 | |||||||
chr3:179657573 | C | T | 1 | a0001c0001t0031g0227 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.168+4180C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657573 | |||||||
chr3:179657574 | A | G | 1 | a0001c0004t0006g0107 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.168+4181A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657574 | |||||||
chr3:179657656 | C | T | 1 | a0001c0004t0006g0226 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.168+4263C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657656 | |||||||
chr3:179657678 | C | T | 10 | a0001c0001t0001g0205 a0001c0001t0004g0206 a0001c0001t0005g0231 others(7): Show |
10 | HG01069.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+4285C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657678 | |||||||
chr3:179657720 | C | T | 4 | a0001c0001t0003g0294 a0001c0001t0003g0296 a0001c0001t0008g0293 others(1): Show |
4 | HG01169.hp1 HG02717.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+4327C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657720 | |||||||
chr3:179657762 | C | CA | 97 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0031 others(94): Show |
97 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.168+4393dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657762 | ||||||
chr3:179657762 | C | CAA | 15 | a0001c0001t0001g0039 a0001c0001t0001g0121 a0001c0001t0001g0203 others(12): Show |
15 | HG00140.hp2 HG01884.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+4392_168+4393d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657762 | ||||||
chr3:179657762 | C | CAAA | 44 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0190 others(41): Show |
44 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.168+4391_168+4393d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657762 | ||||||
chr3:179657762 | C | CAAAA | 7 | a0001c0001t0002g0256 a0001c0001t0003g0208 a0001c0001t0005g0298 others(4): Show |
7 | HG00735.hp1 HG01952.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+4390_168+4393d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657762 | ||||||
chr3:179657762 | CA | C | 8 | a0001c0001t0008g0293 a0001c0001t0022g0257 a0001c0002t0001g0185 others(5): Show |
8 | HG01169.hp1 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+4393delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657762 | ||||||
chr3:179657762 | CAAA | C | 19 | a0001c0001t0001g0201 a0001c0001t0001g0245 a0001c0001t0001g0246 others(16): Show |
19 | HG00438.hp1 HG00438.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.168+4391_168+4393d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657762 | ||||||
chr3:179657762 | CAAAA | C | 7 | a0001c0001t0001g0229 a0001c0001t0006g0228 a0001c0001t0007g0241 others(4): Show |
7 | HG01361.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+4390_168+4393d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657762 | ||||||
chr3:179657762 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0020 a0001c0012t0004g0289 |
2 | HG02145.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.168+4382_168+4393d others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657762 | ||||||
chr3:179657776 | A | AAAAG | 8 | a0001c0001t0004g0105 a0001c0002t0001g0139 a0001c0002t0004g0170 others(5): Show |
9 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+4386_168+4387i others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657776 | ||||||
chr3:179657780 | A | AG | 11 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0146 others(8): Show |
11 | NA18943.hp2 NA18947.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+4387_168+4388i others(3): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657780 | |||||||
chr3:179657780 | A | G | 33 | a0001c0001t0001g0100 a0001c0001t0002g0104 a0001c0001t0004g0234 others(30): Show |
33 | HG00140.hp1 HG01069.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.168+4387A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657780 | |||||||
chr3:179657783 | A | G | 11 | a0001c0001t0004g0105 a0001c0001t0015g0292 a0001c0002t0001g0139 others(8): Show |
12 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+4390A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179657783 | |||||||
chr3:179657842 | TGTGTAGG others(17): Show |
T | 1 | a0001c0016t0004g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.168+4453_168+4476d others(26): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179657842 | ||||||
chr3:179658148 | G | A | 1 | a0001c0001t0008g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.168+4755G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658148 | |||||||
chr3:179658156 | A | G | 15 | a0001c0001t0004g0261 a0001c0001t0005g0202 a0001c0001t0005g0263 others(12): Show |
15 | HG01109.hp2 HG02257.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+4763A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658156 | |||||||
chr3:179658161 | G | A | 1 | a0001c0001t0007g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.168+4768G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658161 | |||||||
chr3:179658201 | A | G | 3 | a0001c0001t0002g0016 a0001c0001t0013g0015 a0001c0004t0006g0226 |
3 | HG00140.hp2 HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.168+4808A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658201 | |||||||
chr3:179658204 | T | G | 1 | a0001c0001t0013g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.168+4811T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658204 | |||||||
chr3:179658274 | A | G | 31 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(28): Show |
31 | HG00438.hp1 HG00738.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.168+4881A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658274 | |||||||
chr3:179658366 | C | T | 2 | a0001c0004t0002g0267 a0001c0006t0002g0138 |
2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.168+4973C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658366 | |||||||
chr3:179658416 | G | T | 70 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0039 others(67): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.168+5023G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658416 | |||||||
chr3:179658419 | T | C | 78 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0034 others(75): Show |
78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.168+5026T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658419 | |||||||
chr3:179658436 | GC | G | 33 | a0001c0001t0001g0205 a0001c0001t0001g0260 a0001c0001t0001g0277 others(30): Show |
34 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.168+5049delC | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179658436 | ||||||
chr3:179658455 | T | C | 1 | a0001c0003t0001g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168+5062T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658455 | |||||||
chr3:179658496 | A | G | 9 | a0001c0001t0004g0018 a0001c0001t0022g0257 a0001c0001t0027g0199 others(6): Show |
9 | HG01433.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+5103A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658496 | |||||||
chr3:179658504 | C | T | 80 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0064 others(77): Show |
80 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.168+5111C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658504 | |||||||
chr3:179658608 | T | C | 1 | a0001c0001t0004g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.168+5215T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658608 | |||||||
chr3:179658738 | AT | A | 5 | a0001c0001t0010g0193 a0001c0001t0010g0194 a0001c0001t0010g0195 others(2): Show |
5 | HG01978.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+5348delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179658738 | ||||||
chr3:179658758 | C | T | 1 | a0001c0001t0006g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.168+5365C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658758 | |||||||
chr3:179658800 | G | A | 1 | a0001c0004t0002g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.168+5407G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658800 | |||||||
chr3:179658854 | A | T | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0284 others(4): Show |
7 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+5461A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658854 | |||||||
chr3:179658911 | G | T | 1 | a0001c0002t0001g0135 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.168+5518G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179658911 | |||||||
chr3:179659169 | A | T | 65 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0001g0082 others(62): Show |
65 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.168+5776A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179659169 | |||||||
chr3:179659364 | T | C | 7 | a0001c0001t0003g0299 a0001c0001t0018g0191 a0001c0002t0001g0137 others(4): Show |
7 | HG00280.hp2 HG01255.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+5971T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179659364 | |||||||
chr3:179659385 | C | T | 261 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(258): Show |
262 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.168+5992C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179659385 | |||||||
chr3:179659404 | G | C | 3 | a0001c0001t0002g0216 a0001c0001t0035g0056 a0001c0002t0041g0124 |
3 | NA18949.hp2 NA18967.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.168+6011G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179659404 | |||||||
chr3:179659451 | G | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.168+6058G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179659451 | |||||||
chr3:179659523 | G | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0030 others(29): Show |
33 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.168+6130G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179659523 | |||||||
chr3:179659550 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.168+6157T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179659550 | |||||||
chr3:179659815 | G | A | 1 | a0001c0001t0004g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.168+6422G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179659815 | |||||||
chr3:179659911 | G | A | 5 | a0001c0003t0005g0002 a0001c0003t0005g0242 a0001c0005t0005g0122 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+6518G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179659911 | |||||||
chr3:179660009 | C | T | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0002g0014 |
3 | NA18999.hp1 NA19007.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.168+6616C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179660009 | |||||||
chr3:179660072 | C | A | 2 | a0001c0001t0001g0277 a0001c0001t0014g0276 |
2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.168+6679C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179660072 | |||||||
chr3:179660105 | A | G | 7 | a0001c0001t0001g0277 a0001c0001t0003g0296 a0001c0001t0014g0276 others(4): Show |
7 | HG02258.hp2 HG02559.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+6712A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179660105 | |||||||
chr3:179660586 | A | G | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.168+7193A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179660586 | |||||||
chr3:179660667 | T | G | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(262): Show |
266 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.168+7274T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179660667 | |||||||
chr3:179660670 | A | G | 1 | a0001c0002t0007g0166 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.168+7277A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179660670 | |||||||
chr3:179660692 | T | G | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.168+7299T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179660692 | |||||||
chr3:179660753 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0030 others(30): Show |
34 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.168+7360G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179660753 | |||||||
chr3:179660980 | G | T | 1 | a0001c0011t0025g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.168+7587G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179660980 | |||||||
chr3:179661023 | A | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.168+7630A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179661023 | |||||||
chr3:179661071 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.168+7678G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179661071 | |||||||
chr3:179661461 | AT | A | 110 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0031 others(107): Show |
110 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.168+8081delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179661461 | ||||||
chr3:179661775 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+8382T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179661775 | |||||||
chr3:179661814 | C | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0031 others(114): Show |
117 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.168+8421C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179661814 | |||||||
chr3:179661876 | A | G | 4 | a0001c0004t0034g0072 a0001c0006t0004g0179 a0001c0006t0006g0181 others(1): Show |
4 | HG03195.hp1 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+8483A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179661876 | |||||||
chr3:179662195 | TA | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0030 others(40): Show |
44 | HG00558.hp2 HG01069.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.168+8804delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179662195 | ||||||
chr3:179662312 | G | T | 1 | a0001c0005t0001g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.168+8919G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179662312 | |||||||
chr3:179662413 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0275 |
2 | HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.168+9020C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179662413 | |||||||
chr3:179662518 | A | T | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.168+9125A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179662518 | |||||||
chr3:179662627 | T | C | 64 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0058 others(61): Show |
64 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.168+9234T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179662627 | |||||||
chr3:179662751 | T | A | 83 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0039 others(80): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.168+9358T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179662751 | |||||||
chr3:179662768 | A | G | 6 | a0001c0001t0001g0203 a0001c0001t0001g0287 a0001c0002t0004g0172 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+9375A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179662768 | |||||||
chr3:179662969 | A | T | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | NA18959.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.168+9576A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179662969 | |||||||
chr3:179662977 | A | T | 2 | a0001c0001t0004g0018 a0001c0001t0004g0234 |
2 | HG01081.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.168+9584A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179662977 | |||||||
chr3:179663100 | A | G | 1 | a0001c0002t0033g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168+9707A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663100 | |||||||
chr3:179663293 | A | G | 1 | a0001c0001t0012g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.168+9900A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663293 | |||||||
chr3:179663317 | C | T | 8 | a0001c0001t0003g0294 a0001c0001t0003g0296 a0001c0001t0004g0266 others(5): Show |
8 | HG01884.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+9924C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663317 | |||||||
chr3:179663409 | C | G | 1 | a0001c0003t0005g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168+10016C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663409 | |||||||
chr3:179663531 | C | T | 1 | a0001c0003t0005g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168+10138C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663531 | |||||||
chr3:179663674 | A | G | 64 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0058 others(61): Show |
64 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.168+10281A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663674 | |||||||
chr3:179663675 | A | G | 12 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0007g0209 others(9): Show |
12 | HG00323.hp1 HG01099.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+10282A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663675 | |||||||
chr3:179663835 | C | T | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.168+10442C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663835 | |||||||
chr3:179663848 | T | C | 61 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0058 others(58): Show |
61 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.168+10455T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663848 | |||||||
chr3:179663887 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA18999.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.168+10494C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663887 | |||||||
chr3:179663924 | C | T | 1 | a0001c0001t0003g0090 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.168+10531C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663924 | |||||||
chr3:179663989 | G | A | 7 | a0001c0001t0001g0203 a0001c0001t0001g0287 a0001c0002t0004g0172 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+10596G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179663989 | |||||||
chr3:179664001 | A | G | 6 | a0001c0001t0001g0203 a0001c0001t0001g0287 a0001c0002t0004g0172 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+10608A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179664001 | |||||||
chr3:179664079 | G | A | 263 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(260): Show |
264 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.168+10686G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179664079 | |||||||
chr3:179664130 | GT | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0064 others(15): Show |
18 | HG00558.hp1 HG01109.hp2 HG02293.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+10750delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179664130 | ||||||
chr3:179664640 | C | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(93): Show |
97 | HG00558.hp1 HG00558.hp2 HG01069.hp2 others(94): Show |
intron_variant | MODIFIER | c.168+11247C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179664640 | |||||||
chr3:179664723 | T | C | 3 | a0001c0001t0004g0105 a0001c0001t0017g0192 a0001c0001t0030g0258 |
3 | HG02809.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.168+11330T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179664723 | |||||||
chr3:179664735 | C | T | 260 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(257): Show |
261 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.168+11342C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179664735 | |||||||
chr3:179664794 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.168+11401T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179664794 | |||||||
chr3:179665019 | C | T | 11 | a0001c0001t0002g0007 a0001c0001t0007g0209 a0001c0004t0002g0182 others(8): Show |
11 | HG01099.hp1 HG01361.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+11626C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665019 | |||||||
chr3:179665020 | G | A | 1 | a0001c0002t0009g0141 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.168+11627G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665020 | |||||||
chr3:179665047 | A | G | 1 | a0001c0001t0005g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.168+11654A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665047 | |||||||
chr3:179665064 | G | A | 71 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0039 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.168+11671G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665064 | |||||||
chr3:179665251 | C | T | 7 | a0001c0001t0002g0007 a0001c0001t0007g0209 a0001c0004t0002g0182 others(4): Show |
7 | HG01099.hp1 HG01361.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+11858C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665251 | |||||||
chr3:179665562 | C | T | 1 | a0001c0002t0005g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.168+12169C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665562 | |||||||
chr3:179665679 | C | T | 8 | a0001c0001t0001g0203 a0001c0001t0001g0219 a0001c0001t0001g0287 others(5): Show |
8 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+12286C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665679 | |||||||
chr3:179665753 | T | C | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.168+12360T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665753 | |||||||
chr3:179665978 | G | C | 78 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0039 others(75): Show |
78 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.168+12585G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665978 | |||||||
chr3:179665980 | G | A | 7 | a0001c0001t0001g0203 a0001c0001t0001g0287 a0001c0002t0004g0172 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+12587G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179665980 | |||||||
chr3:179666013 | C | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0064 others(15): Show |
18 | HG00558.hp1 HG01109.hp2 HG02293.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+12620C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179666013 | |||||||
chr3:179666120 | G | A | 181 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(178): Show |
182 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.168+12727G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179666120 | |||||||
chr3:179666573 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.168+13180C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179666573 | |||||||
chr3:179666661 | C | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0275 a0001c0001t0001g0282 |
3 | HG01169.hp2 HG02738.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.168+13268C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179666661 | |||||||
chr3:179666758 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.168+13365C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179666758 | |||||||
chr3:179666876 | A | G | 10 | a0001c0001t0006g0297 a0001c0001t0008g0198 a0001c0001t0015g0292 others(7): Show |
10 | HG00735.hp1 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+13483A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179666876 | |||||||
chr3:179667150 | G | A | 8 | a0001c0001t0003g0294 a0001c0001t0003g0296 a0001c0001t0004g0266 others(5): Show |
8 | HG01884.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+13757G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179667150 | |||||||
chr3:179667212 | C | T | 145 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0031 others(142): Show |
145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.168+13819C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179667212 | |||||||
chr3:179667224 | A | G | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.168+13831A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179667224 | |||||||
chr3:179667242 | G | GT | 63 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0058 others(60): Show |
63 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.168+13850dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179667242 | ||||||
chr3:179667519 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.168+14126G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179667519 | |||||||
chr3:179667720 | C | T | 5 | a0001c0001t0006g0297 a0001c0001t0015g0292 a0001c0002t0004g0143 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-14158C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179667720 | |||||||
chr3:179667723 | C | T | 1 | a0001c0002t0009g0141 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.169-14155C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179667723 | |||||||
chr3:179667771 | T | C | 63 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0058 others(60): Show |
63 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-14107T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179667771 | |||||||
chr3:179667848 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0075 others(3): Show |
6 | HG02015.hp1 HG02074.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-14030A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179667848 | |||||||
chr3:179668396 | C | A | 1 | a0001c0002t0001g0152 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.169-13482C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179668396 | |||||||
chr3:179668422 | G | A | 1 | a0001c0001t0002g0272 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.169-13456G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179668422 | |||||||
chr3:179668440 | A | C | 63 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0058 others(60): Show |
63 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.169-13438A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179668440 | |||||||
chr3:179668440 | A | G | 3 | a0001c0002t0004g0170 a0001c0002t0005g0171 a0001c0002t0006g0169 |
3 | HG02572.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169-13438A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179668440 | |||||||
chr3:179668709 | A | T | 9 | a0001c0001t0006g0297 a0001c0001t0008g0198 a0001c0001t0015g0292 others(6): Show |
9 | HG00735.hp1 HG01109.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-13169A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179668709 | |||||||
chr3:179668753 | A | G | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.169-13125A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179668753 | |||||||
chr3:179668927 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.169-12951C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179668927 | |||||||
chr3:179668956 | A | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0030 others(43): Show |
47 | HG00558.hp2 HG01069.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.169-12922A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179668956 | |||||||
chr3:179669097 | T | C | 1 | a0001c0002t0009g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.169-12781T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669097 | |||||||
chr3:179669232 | A | G | 65 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0058 others(62): Show |
65 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.169-12646A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669232 | |||||||
chr3:179669243 | C | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0064 others(15): Show |
18 | HG00558.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.169-12635C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669243 | |||||||
chr3:179669325 | C | T | 71 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0039 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.169-12553C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669325 | |||||||
chr3:179669347 | C | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0064 others(15): Show |
18 | HG00558.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.169-12531C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669347 | |||||||
chr3:179669384 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-12494C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669384 | |||||||
chr3:179669385 | A | G | 253 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(250): Show |
254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.169-12493A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669385 | |||||||
chr3:179669426 | T | C | 72 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0039 others(69): Show |
72 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.169-12452T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669426 | |||||||
chr3:179669488 | A | T | 74 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0039 others(71): Show |
74 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.169-12390A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669488 | |||||||
chr3:179669511 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0014g0276 |
2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.169-12367C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669511 | |||||||
chr3:179669758 | G | T | 34 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0203 others(31): Show |
34 | HG00280.hp2 HG00642.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.169-12120G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669758 | |||||||
chr3:179669832 | AC | A | 71 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0039 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.169-12038delC | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179669832 | ||||||
chr3:179669843 | C | A | 12 | a0001c0001t0002g0007 a0001c0001t0007g0209 a0001c0002t0001g0134 others(9): Show |
12 | HG01099.hp1 HG01361.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-12035C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179669843 | |||||||
chr3:179670006 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.169-11872C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670006 | |||||||
chr3:179670006 | C | CCT | 32 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0064 others(29): Show |
32 | HG00558.hp1 HG01109.hp2 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.169-11871_169-1187 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179670006 | ||||||
chr3:179670009 | G | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0064 others(29): Show |
32 | HG00558.hp1 HG01109.hp2 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.169-11869G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670009 | |||||||
chr3:179670094 | G | T | 252 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(249): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.169-11784G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670094 | |||||||
chr3:179670198 | G | A | 1 | a0001c0001t0003g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.169-11680G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670198 | |||||||
chr3:179670202 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.169-11676C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670202 | |||||||
chr3:179670207 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.169-11671C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670207 | |||||||
chr3:179670506 | A | G | 1 | a0001c0001t0005g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.169-11372A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670506 | |||||||
chr3:179670618 | C | T | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(262): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.169-11260C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670618 | |||||||
chr3:179670629 | A | G | 2 | a0001c0001t0005g0202 a0001c0001t0005g0263 |
2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.169-11249A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670629 | |||||||
chr3:179670642 | A | C | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.169-11236A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670642 | |||||||
chr3:179670691 | A | AT | 126 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0048 others(123): Show |
126 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.169-11180dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179670691 | ||||||
chr3:179670721 | A | T | 132 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0048 others(129): Show |
132 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.169-11157A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670721 | |||||||
chr3:179670760 | T | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0212 a0001c0001t0001g0259 |
3 | HG00621.hp2 NA18941.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.169-11118T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670760 | |||||||
chr3:179670767 | C | T | 1 | a0001c0001t0004g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.169-11111C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179670767 | |||||||
chr3:179671073 | C | T | 3 | a0001c0001t0005g0231 a0001c0001t0005g0233 a0001c0001t0006g0240 |
3 | HG02055.hp1 HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.169-10805C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671073 | |||||||
chr3:179671177 | C | T | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.169-10701C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671177 | |||||||
chr3:179671344 | G | A | 1 | a0001c0001t0006g0288 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.169-10534G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671344 | |||||||
chr3:179671526 | A | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(55): Show |
59 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.169-10352A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671526 | |||||||
chr3:179671670 | T | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(75): Show |
79 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.169-10208T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671670 | |||||||
chr3:179671685 | T | C | 3 | a0001c0001t0004g0261 a0001c0001t0006g0288 a0001c0001t0023g0262 |
3 | HG02965.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.169-10193T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671685 | |||||||
chr3:179671726 | A | T | 11 | a0001c0001t0004g0261 a0001c0001t0005g0202 a0001c0001t0005g0231 others(8): Show |
11 | HG01433.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-10152A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671726 | |||||||
chr3:179671807 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.169-10071C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671807 | |||||||
chr3:179671827 | G | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(55): Show |
59 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.169-10051G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671827 | |||||||
chr3:179671868 | C | T | 55 | a0001c0001t0001g0032 a0001c0001t0001g0058 a0001c0001t0001g0082 others(52): Show |
55 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.169-10010C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671868 | |||||||
chr3:179671869 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0220 |
2 | HG00558.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.169-10009G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179671869 | |||||||
chr3:179672068 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(56): Show |
60 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.169-9810A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179672068 | |||||||
chr3:179672104 | A | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(62): Show |
66 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.169-9774A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179672104 | |||||||
chr3:179672130 | T | C | 1 | a0001c0002t0001g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-9748T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179672130 | |||||||
chr3:179672255 | T | C | 108 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(105): Show |
108 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.169-9623T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179672255 | |||||||
chr3:179672501 | C | T | 1 | a0001c0006t0004g0179 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-9377C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179672501 | |||||||
chr3:179672512 | ATAGCTGG others(41): Show |
A | 1 | a0001c0001t0007g0099 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.169-9339_169-9292d others(50): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179672512 | ||||||
chr3:179672594 | G | A | 1 | a0001c0001t0026g0049 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.169-9284G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179672594 | |||||||
chr3:179672885 | A | G | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.169-8993A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179672885 | |||||||
chr3:179672892 | T | C | 2 | a0001c0004t0002g0267 a0001c0006t0002g0138 |
2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.169-8986T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179672892 | |||||||
chr3:179673016 | T | C | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.169-8862T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179673016 | |||||||
chr3:179673083 | A | G | 1 | a0003c0010t0009g0069 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.169-8795A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179673083 | |||||||
chr3:179673150 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.169-8728A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179673150 | |||||||
chr3:179673351 | A | T | 14 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0008g0040 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-8527A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179673351 | |||||||
chr3:179673400 | GC | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(275): Show |
279 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.169-8471delC | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179673400 | ||||||
chr3:179673532 | T | G | 120 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0050 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.169-8346T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179673532 | |||||||
chr3:179673770 | G | A | 1 | a0001c0001t0005g0232 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.169-8108G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179673770 | |||||||
chr3:179673774 | G | A | 57 | a0001c0001t0001g0032 a0001c0001t0001g0058 a0001c0001t0001g0082 others(54): Show |
57 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.169-8104G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179673774 | |||||||
chr3:179673915 | G | C | 1 | a0001c0001t0002g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.169-7963G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179673915 | |||||||
chr3:179673978 | C | T | 4 | a0001c0001t0001g0260 a0001c0001t0003g0294 a0001c0001t0017g0192 others(1): Show |
4 | HG02486.hp1 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-7900C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179673978 | |||||||
chr3:179674366 | G | A | 108 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0050 others(105): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.169-7512G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179674366 | |||||||
chr3:179674448 | A | G | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.169-7430A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179674448 | |||||||
chr3:179674565 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.169-7313T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179674565 | |||||||
chr3:179674620 | GT | G | 107 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0050 others(104): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.169-7247delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179674620 | ||||||
chr3:179674720 | A | G | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.169-7158A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179674720 | |||||||
chr3:179674721 | T | G | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.169-7157T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179674721 | |||||||
chr3:179674901 | T | C | 4 | a0001c0004t0034g0072 a0001c0006t0004g0179 a0001c0006t0006g0181 others(1): Show |
4 | HG03195.hp1 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-6977T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179674901 | |||||||
chr3:179675036 | A | G | 2 | a0001c0001t0002g0120 a0001c0002t0002g0147 |
2 | NA18943.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.169-6842A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179675036 | |||||||
chr3:179675246 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0121 a0001c0001t0001g0249 others(2): Show |
5 | NA18954.hp1 NA18986.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-6632G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179675246 | |||||||
chr3:179675262 | GT | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(53): Show |
57 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.169-6612delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179675262 | ||||||
chr3:179675536 | T | TTTA | 126 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(123): Show |
127 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.169-6315_169-6313d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179675536 | ||||||
chr3:179675536 | T | TTTATTA | 20 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0096 others(17): Show |
20 | HG00323.hp1 HG00738.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.169-6318_169-6313d others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179675536 | ||||||
chr3:179675536 | T | TTTATTAT others(2): Show |
4 | a0001c0001t0007g0209 a0001c0004t0006g0107 a0001c0004t0034g0072 others(1): Show |
4 | HG01099.hp1 HG01361.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-6321_169-6313d others(11): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179675536 | ||||||
chr3:179675536 | T | TTTATTAT others(5): Show |
3 | a0001c0004t0006g0226 a0001c0006t0006g0181 a0001c0006t0032g0140 |
3 | HG00140.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.169-6324_169-6313d others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179675536 | ||||||
chr3:179675539 | A | T | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.169-6339A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179675539 | |||||||
chr3:179675641 | G | A | 5 | a0001c0001t0001g0260 a0001c0001t0003g0294 a0001c0001t0003g0296 others(2): Show |
5 | HG02486.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-6237G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179675641 | |||||||
chr3:179675662 | C | T | 1 | a0001c0002t0003g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-6216C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179675662 | |||||||
chr3:179675697 | T | G | 281 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(278): Show |
282 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.169-6181T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179675697 | |||||||
chr3:179675823 | C | T | 1 | a0001c0009t0005g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.169-6055C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179675823 | |||||||
chr3:179675985 | A | G | 25 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0004g0261 others(22): Show |
25 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.169-5893A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179675985 | |||||||
chr3:179676040 | A | C | 1 | a0001c0002t0003g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-5838A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179676040 | |||||||
chr3:179676049 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.169-5829T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179676049 | |||||||
chr3:179676143 | G | A | 1 | a0001c0002t0005g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.169-5735G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179676143 | |||||||
chr3:179676208 | C | T | 1 | a0001c0002t0003g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-5670C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179676208 | |||||||
chr3:179676335 | T | G | 48 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(45): Show |
48 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-5543T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179676335 | |||||||
chr3:179676438 | T | C | 1 | a0001c0001t0003g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.169-5440T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179676438 | |||||||
chr3:179676475 | A | G | 1 | a0001c0002t0003g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-5403A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179676475 | |||||||
chr3:179676557 | C | A | 41 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(38): Show |
41 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.169-5321C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179676557 | |||||||
chr3:179676728 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.169-5150G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179676728 | |||||||
chr3:179677109 | C | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169-4769C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179677109 | |||||||
chr3:179677201 | C | T | 1 | a0001c0002t0003g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-4677C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179677201 | |||||||
chr3:179677243 | C | A | 7 | a0001c0001t0001g0260 a0001c0001t0003g0294 a0001c0001t0003g0296 others(4): Show |
7 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-4635C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179677243 | |||||||
chr3:179677410 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.169-4468G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179677410 | |||||||
chr3:179677495 | A | G | 213 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0031 others(210): Show |
213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.169-4383A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179677495 | |||||||
chr3:179677711 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.169-4167A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179677711 | |||||||
chr3:179677789 | G | T | 1 | a0001c0001t0002g0086 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.169-4089G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179677789 | |||||||
chr3:179677837 | G | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169-4041G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179677837 | |||||||
chr3:179677848 | A | G | 18 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0053 others(15): Show |
18 | HG00673.hp1 HG00738.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.169-4030A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179677848 | |||||||
chr3:179678018 | C | T | 1 | a0001c0002t0009g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.169-3860C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179678018 | |||||||
chr3:179678218 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.169-3660A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179678218 | |||||||
chr3:179678281 | G | A | 108 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0050 others(105): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.169-3597G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179678281 | |||||||
chr3:179678343 | T | G | 1 | a0001c0001t0019g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.169-3535T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179678343 | |||||||
chr3:179678438 | A | G | 2 | a0001c0002t0016g0173 a0001c0002t0033g0174 |
2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.169-3440A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179678438 | |||||||
chr3:179678478 | A | AT | 74 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0050 others(71): Show |
74 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.169-3388dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179678478 | ||||||
chr3:179678478 | A | ATT | 16 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0008g0040 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.169-3389_169-3388d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179678478 | ||||||
chr3:179678735 | G | T | 2 | a0001c0001t0003g0296 a0001c0003t0001g0255 |
2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.169-3143G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179678735 | |||||||
chr3:179678799 | C | T | 165 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0048 others(162): Show |
165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.169-3079C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179678799 | |||||||
chr3:179678922 | C | T | 164 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0048 others(161): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.169-2956C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179678922 | |||||||
chr3:179679022 | C | T | 1 | a0001c0002t0009g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.169-2856C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179679022 | |||||||
chr3:179679057 | G | A | 138 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0048 others(135): Show |
138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.169-2821G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179679057 | |||||||
chr3:179679094 | T | TAGAAATT others(365): Show |
1 | a0001c0003t0001g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169-2769_169-2768i others(374): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179679094 | ||||||
chr3:179679147 | T | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0075 a0001c0001t0001g0251 |
3 | HG02015.hp1 HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.169-2731T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179679147 | |||||||
chr3:179679407 | A | G | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.169-2471A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179679407 | |||||||
chr3:179679646 | A | T | 1 | a0001c0002t0003g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.169-2232A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179679646 | |||||||
chr3:179679794 | GT | G | 20 | a0001c0001t0001g0205 a0001c0001t0001g0225 a0001c0001t0001g0284 others(17): Show |
20 | HG01070.hp2 HG01074.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.169-2057delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179679794 | ||||||
chr3:179679794 | GTT | G | 122 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0048 others(119): Show |
123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.169-2058_169-2057d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179679794 | ||||||
chr3:179679794 | GTTT | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(70): Show |
73 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.169-2059_169-2057d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179679794 | ||||||
chr3:179679794 | GTTTT | G | 14 | a0001c0001t0001g0286 a0001c0001t0003g0294 a0001c0001t0003g0296 others(11): Show |
14 | HG01071.hp2 HG01109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-2060_169-2057d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179679794 | ||||||
chr3:179679794 | GTTTTTTT others(3): Show |
G | 46 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(43): Show |
46 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.169-2066_169-2057d others(12): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179679794 | ||||||
chr3:179679794 | GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0003g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.169-2069_169-2057d others(15): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179679794 | ||||||
chr3:179679808 | T | G | 13 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0004t0002g0182 others(10): Show |
13 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.169-2070T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179679808 | |||||||
chr3:179680036 | A | G | 7 | a0001c0001t0001g0260 a0001c0001t0003g0294 a0001c0001t0003g0296 others(4): Show |
7 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-1842A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680036 | |||||||
chr3:179680045 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.169-1833C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680045 | |||||||
chr3:179680104 | C | T | 122 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(119): Show |
123 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.169-1774C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680104 | |||||||
chr3:179680136 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169-1742A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680136 | |||||||
chr3:179680164 | C | T | 66 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0050 others(63): Show |
66 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.169-1714C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680164 | |||||||
chr3:179680173 | A | AAAC | 17 | a0001c0001t0001g0287 a0001c0001t0002g0007 a0001c0001t0002g0097 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.169-1678_169-1676d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179680173 | ||||||
chr3:179680173 | A | AAACAAC | 7 | a0001c0001t0031g0227 a0001c0002t0005g0136 a0001c0003t0005g0002 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-1681_169-1676d others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179680173 | ||||||
chr3:179680173 | A | AAACAACA others(2): Show |
28 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0039 others(25): Show |
28 | HG00558.hp1 HG00642.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.169-1684_169-1676d others(11): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179680173 | ||||||
chr3:179680173 | A | AAACAACA others(5): Show |
7 | a0001c0001t0001g0034 a0001c0001t0001g0094 a0001c0001t0001g0212 others(4): Show |
7 | HG00621.hp2 HG02165.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-1687_169-1676d others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179680173 | ||||||
chr3:179680173 | A | AAACAACA others(11): Show |
5 | a0001c0001t0001g0222 a0001c0001t0002g0089 a0001c0001t0002g0120 others(2): Show |
5 | HG01257.hp2 NA18943.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-1693_169-1676d others(20): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179680173 | ||||||
chr3:179680173 | AAAC | A | 61 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(58): Show |
62 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.169-1678_169-1676d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179680173 | ||||||
chr3:179680173 | AAACAAC | A | 58 | a0001c0001t0001g0032 a0001c0001t0001g0058 a0001c0001t0001g0082 others(55): Show |
58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.169-1681_169-1676d others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 179680173 | ||||||
chr3:179680212 | G | A | 222 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(219): Show |
223 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.169-1666G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680212 | |||||||
chr3:179680319 | C | T | 280 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(277): Show |
281 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.169-1559C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680319 | |||||||
chr3:179680411 | C | T | 2 | a0001c0001t0014g0184 a0001c0011t0025g0183 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.169-1467C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680411 | |||||||
chr3:179680429 | C | T | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.169-1449C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680429 | |||||||
chr3:179680430 | G | A | 1 | a0001c0002t0029g0128 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.169-1448G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680430 | |||||||
chr3:179680439 | G | A | 222 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(219): Show |
223 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.169-1439G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680439 | |||||||
chr3:179680479 | T | A | 14 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0007g0209 others(11): Show |
14 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-1399T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680479 | |||||||
chr3:179680549 | CA | C | 8 | a0001c0001t0001g0260 a0001c0001t0003g0294 a0001c0001t0003g0296 others(5): Show |
8 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-1328delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680549 | |||||||
chr3:179680551 | T | G | 8 | a0001c0001t0001g0260 a0001c0001t0003g0294 a0001c0001t0003g0296 others(5): Show |
8 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-1327T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680551 | |||||||
chr3:179680569 | C | G | 7 | a0001c0001t0001g0260 a0001c0001t0003g0294 a0001c0001t0003g0296 others(4): Show |
7 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-1309C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680569 | |||||||
chr3:179680572 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.169-1306A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680572 | |||||||
chr3:179680821 | ATGAGTCA others(178): Show |
A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(53): Show |
56 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.169-1056_169-872de others(1): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680821 | |||||||
chr3:179680909 | C | A | 1 | a0001c0001t0003g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.169-969C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680909 | |||||||
chr3:179680937 | A | G | 63 | a0001c0001t0001g0032 a0001c0001t0001g0048 a0001c0001t0001g0058 others(60): Show |
63 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.169-941A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680937 | |||||||
chr3:179680998 | A | C | 14 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0007g0209 others(11): Show |
14 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-880A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179680998 | |||||||
chr3:179681008 | C | T | 56 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(53): Show |
56 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.169-870C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681008 | |||||||
chr3:179681009 | A | T | 56 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(53): Show |
56 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.169-869A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681009 | |||||||
chr3:179681010 | A | C | 14 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0007g0209 others(11): Show |
14 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-868A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681010 | |||||||
chr3:179681010 | A | T | 56 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(53): Show |
56 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.169-868A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681010 | |||||||
chr3:179681080 | G | T | 1 | a0001c0002t0040g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.169-798G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681080 | |||||||
chr3:179681438 | G | T | 60 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(57): Show |
60 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.169-440G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681438 | |||||||
chr3:179681519 | G | T | 2 | a0001c0001t0002g0045 a0001c0002t0002g0149 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.169-359G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681519 | |||||||
chr3:179681588 | A | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(55): Show |
59 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.169-290A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681588 | |||||||
chr3:179681624 | A | C | 1 | a0001c0002t0003g0123 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.169-254A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681624 | |||||||
chr3:179681782 | C | T | 131 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(128): Show |
131 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.169-96C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681782 | |||||||
chr3:179681867 | C | T | 4 | a0001c0003t0039g0019 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-11C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 1/20 | chr3 | 179681867 | |||||||
chr3:179682011 | C | T | 2 | a0001c0002t0003g0158 a0001c0003t0001g0230 |
2 | HG01433.hp1 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.294+8C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682011 | |||||||
chr3:179682034 | T | C | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.294+31T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682034 | |||||||
chr3:179682158 | A | G | 52 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(49): Show |
52 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.294+155A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682158 | |||||||
chr3:179682247 | G | GAAA | 100 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0032 others(97): Show |
100 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.294+252_294+254dup others(3): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179682247 | ||||||
chr3:179682247 | G | GAAAA | 55 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(52): Show |
55 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.294+251_294+254dup others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179682247 | ||||||
chr3:179682257 | A | AC | 15 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0007g0209 others(12): Show |
15 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.294+256dupC | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179682257 | ||||||
chr3:179682307 | C | T | 173 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(170): Show |
173 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.294+304C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682307 | |||||||
chr3:179682316 | T | TA | 154 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(151): Show |
154 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.294+322dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179682316 | ||||||
chr3:179682326 | C | A | 1 | a0001c0001t0001g0280 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.294+323C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682326 | |||||||
chr3:179682328 | A | G | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.294+325A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682328 | |||||||
chr3:179682385 | GCTTC | G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(170): Show |
173 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.294+386_294+389del others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179682385 | ||||||
chr3:179682415 | C | T | 1 | a0001c0002t0001g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.294+412C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682415 | |||||||
chr3:179682557 | C | T | 51 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(48): Show |
51 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.294+554C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682557 | |||||||
chr3:179682567 | T | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0041 others(30): Show |
33 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.294+564T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682567 | |||||||
chr3:179682593 | G | A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(154): Show |
157 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.294+590G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682593 | |||||||
chr3:179682674 | G | A | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.294+671G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682674 | |||||||
chr3:179682947 | T | G | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.294+944T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179682947 | |||||||
chr3:179683049 | T | C | 1 | a0001c0003t0001g0230 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.294+1046T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179683049 | |||||||
chr3:179683308 | T | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(45): Show |
48 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.294+1305T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179683308 | |||||||
chr3:179683357 | T | C | 15 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0007g0209 others(12): Show |
15 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.294+1354T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179683357 | |||||||
chr3:179683624 | A | C | 2 | a0001c0001t0014g0184 a0001c0011t0025g0183 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+1621A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179683624 | |||||||
chr3:179683762 | T | C | 283 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(280): Show |
284 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.294+1759T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179683762 | |||||||
chr3:179684034 | C | T | 158 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(155): Show |
158 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.294+2031C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684034 | |||||||
chr3:179684070 | C | T | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.294+2067C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684070 | |||||||
chr3:179684107 | C | T | 55 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(52): Show |
55 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.294+2104C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684107 | |||||||
chr3:179684108 | G | A | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.294+2105G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684108 | |||||||
chr3:179684189 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.294+2186G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684189 | |||||||
chr3:179684201 | C | T | 18 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0053 others(15): Show |
18 | HG00673.hp1 HG00738.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.294+2198C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684201 | |||||||
chr3:179684261 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.294+2258A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684261 | |||||||
chr3:179684270 | T | TAC | 30 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0080 others(27): Show |
30 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.294+2309_294+2310d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684270 | ||||||
chr3:179684270 | T | TACAC | 85 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0041 others(82): Show |
85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.294+2307_294+2310d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684270 | ||||||
chr3:179684270 | T | TACACAC | 39 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0064 others(36): Show |
39 | HG00642.hp2 HG01175.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.294+2305_294+2310d others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684270 | ||||||
chr3:179684270 | T | TACACACA others(1): Show |
22 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0048 others(19): Show |
22 | HG00558.hp1 HG01099.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.294+2303_294+2310d others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684270 | ||||||
chr3:179684270 | T | TACACACA others(3): Show |
11 | a0001c0001t0001g0032 a0001c0001t0001g0219 a0001c0001t0001g0249 others(8): Show |
11 | HG02074.hp1 HG02155.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.294+2301_294+2310d others(12): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684270 | ||||||
chr3:179684270 | T | TACACACA others(5): Show |
2 | a0001c0002t0001g0159 a0001c0004t0034g0072 |
2 | HG03516.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.294+2299_294+2310d others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684270 | ||||||
chr3:179684270 | TAC | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0093 a0001c0001t0001g0100 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.294+2309_294+2310d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684270 | ||||||
chr3:179684270 | TACAC | T | 4 | a0001c0001t0001g0260 a0001c0001t0001g0274 a0001c0003t0005g0002 others(1): Show |
4 | HG01975.hp1 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+2307_294+2310d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684270 | ||||||
chr3:179684270 | TACACACA others(11): Show |
T | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.294+2293_294+2310d others(20): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684270 | ||||||
chr3:179684278 | C | CACACACA others(5): Show |
1 | a0001c0002t0001g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.294+2286_294+2287i others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684278 | ||||||
chr3:179684280 | C | CACACACA others(3): Show |
49 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(46): Show |
49 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.294+2286_294+2287i others(12): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684280 | ||||||
chr3:179684284 | C | CACACAG | 3 | a0001c0001t0002g0067 a0001c0001t0021g0295 a0001c0002t0001g0163 |
3 | HG01358.hp1 HG01358.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.294+2286_294+2287i others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684284 | ||||||
chr3:179684358 | T | A | 1 | a0001c0001t0002g0044 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.294+2355T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684358 | |||||||
chr3:179684394 | T | A | 283 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(280): Show |
284 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.294+2391T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684394 | |||||||
chr3:179684779 | CT | C | 282 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(279): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.294+2787delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179684779 | ||||||
chr3:179684821 | T | A | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.294+2818T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684821 | |||||||
chr3:179684952 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.294+2949T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684952 | |||||||
chr3:179684983 | G | T | 1 | a0001c0001t0009g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.294+2980G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179684983 | |||||||
chr3:179685165 | AT | A | 95 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0030 others(92): Show |
96 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.294+3172delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179685165 | ||||||
chr3:179685184 | A | G | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.294+3181A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179685184 | |||||||
chr3:179685187 | AT | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(45): Show |
48 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.294+3195delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179685187 | ||||||
chr3:179685411 | T | A | 1 | a0001c0001t0001g0031 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.294+3408T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179685411 | |||||||
chr3:179685547 | T | C | 1 | a0001c0001t0003g0294 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.294+3544T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179685547 | |||||||
chr3:179685631 | TA | T | 8 | a0001c0001t0001g0050 a0001c0001t0002g0045 a0001c0001t0002g0216 others(5): Show |
8 | HG01975.hp2 HG02735.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+3644delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179685631 | ||||||
chr3:179685693 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.294+3690A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179685693 | |||||||
chr3:179685971 | C | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(46): Show |
49 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.294+3968C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179685971 | |||||||
chr3:179686019 | C | A | 1 | a0001c0002t0001g0159 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.294+4016C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179686019 | |||||||
chr3:179686058 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.294+4055C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179686058 | |||||||
chr3:179686195 | C | T | 1 | a0001c0001t0006g0273 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.295-4046C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179686195 | |||||||
chr3:179686583 | A | G | 14 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
14 | HG00673.hp1 HG01928.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.295-3658A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179686583 | |||||||
chr3:179686627 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.295-3614C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179686627 | |||||||
chr3:179686885 | C | T | 96 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0030 others(93): Show |
97 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.295-3356C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179686885 | |||||||
chr3:179686903 | G | T | 1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.295-3338G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179686903 | |||||||
chr3:179687036 | C | T | 54 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(51): Show |
54 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.295-3205C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179687036 | |||||||
chr3:179687442 | C | T | 1 | a0001c0001t0005g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295-2799C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179687442 | |||||||
chr3:179687509 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.295-2732A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179687509 | |||||||
chr3:179687600 | G | A | 1 | a0001c0001t0002g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.295-2641G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179687600 | |||||||
chr3:179687659 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0020 a0001c0001t0004g0105 a0001c0001t0004g0236 others(3): Show |
6 | HG01256.hp2 HG01258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-2563_295-2556d others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0280 a0001c0003t0005g0242 a0001c0005t0005g0122 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-2565_295-2556d others(12): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0031 a0001c0001t0004g0261 a0001c0002t0004g0186 others(1): Show |
4 | HG00558.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-2566_295-2556d others(13): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(5): Show |
18 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0041 others(15): Show |
18 | HG02015.hp1 HG02132.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.295-2567_295-2556d others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(6): Show |
34 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0063 others(31): Show |
34 | HG00621.hp2 HG00642.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.295-2568_295-2556d others(15): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(7): Show |
17 | a0001c0001t0001g0034 a0001c0001t0001g0064 a0001c0001t0001g0080 others(14): Show |
17 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.295-2569_295-2556d others(16): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(8): Show |
33 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(30): Show |
33 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.295-2570_295-2556d others(17): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(9): Show |
28 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0110 others(25): Show |
28 | HG01256.hp1 HG01358.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.295-2571_295-2556d others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(10): Show |
15 | a0001c0001t0001g0055 a0001c0001t0001g0078 a0001c0001t0001g0211 others(12): Show |
16 | HG00140.hp2 HG00621.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.295-2572_295-2556d others(19): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(11): Show |
7 | a0001c0001t0001g0030 a0001c0001t0002g0036 a0001c0001t0002g0097 others(4): Show |
7 | HG00323.hp1 HG00558.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-2573_295-2556d others(20): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(12): Show |
7 | a0001c0001t0003g0299 a0001c0001t0005g0202 a0001c0001t0005g0298 others(4): Show |
7 | HG01192.hp2 HG02145.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-2574_295-2556d others(21): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(13): Show |
5 | a0001c0001t0005g0263 a0001c0001t0018g0191 a0001c0005t0001g0150 others(2): Show |
5 | HG01255.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-2575_295-2556d others(22): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(14): Show |
3 | a0001c0001t0008g0293 a0001c0003t0001g0290 a0003c0010t0009g0102 |
3 | HG01169.hp1 HG03490.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.295-2576_295-2556d others(23): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0260 a0001c0002t0001g0185 |
3 | HG01123.hp1 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.295-2577_295-2556d others(24): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0007g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.295-2579_295-2556d others(26): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(18): Show |
3 | a0001c0001t0002g0012 a0001c0001t0002g0060 a0001c0001t0012g0070 |
3 | HG03239.hp2 NA18943.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.295-2580_295-2556d others(27): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(19): Show |
6 | a0001c0001t0001g0201 a0001c0001t0002g0086 a0001c0001t0004g0018 others(3): Show |
6 | HG00438.hp1 HG01175.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-2581_295-2556d others(28): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(20): Show |
6 | a0001c0001t0001g0032 a0001c0001t0001g0048 a0001c0001t0001g0278 others(3): Show |
6 | HG01074.hp1 HG01099.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-2556_295-2555i others(29): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(21): Show |
4 | a0001c0001t0001g0207 a0001c0001t0006g0081 a0001c0001t0007g0099 others(1): Show |
4 | HG00323.hp2 HG02280.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-2556_295-2555i others(30): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(23): Show |
3 | a0001c0001t0004g0234 a0001c0001t0007g0013 a0001c0002t0001g0135 |
3 | HG00741.hp2 HG01069.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.295-2556_295-2555i others(32): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0035g0056 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.295-2556_295-2555i others(33): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(25): Show |
3 | a0001c0001t0001g0058 a0001c0001t0001g0218 a0001c0001t0002g0011 |
3 | HG00597.hp2 HG03927.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.295-2556_295-2555i others(34): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(26): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0229 |
2 | HG01361.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.295-2556_295-2555i others(35): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(27): Show |
1 | a0001c0001t0006g0228 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.295-2556_295-2555i others(36): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(28): Show |
3 | a0001c0001t0002g0216 a0001c0001t0011g0057 a0001c0002t0007g0166 |
3 | NA19055.hp1 NA19055.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.295-2556_295-2555i others(37): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(29): Show |
2 | a0001c0001t0011g0224 a0004c0013t0001g0010 |
2 | NA18612.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.295-2556_295-2555i others(38): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(30): Show |
2 | a0001c0002t0001g0137 a0001c0002t0041g0124 |
2 | HG00280.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.295-2556_295-2555i others(39): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-2556_295-2555i others(41): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | C | CAAAAAAA others(37): Show |
1 | a0001c0001t0002g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.295-2556_295-2555i others(46): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | CA | C | 6 | a0001c0001t0001g0284 a0001c0001t0007g0241 a0001c0001t0010g0193 others(3): Show |
6 | HG01192.hp1 HG01978.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-2556delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687659 | CAAAAAAA others(2): Show |
C | 16 | a0001c0001t0001g0068 a0001c0001t0003g0009 a0001c0001t0005g0017 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.295-2564_295-2556d others(11): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179687659 | ||||||
chr3:179687755 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.295-2486T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179687755 | |||||||
chr3:179687811 | C | G | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0071 others(1): Show |
4 | HG00621.hp1 HG02080.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-2430C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179687811 | |||||||
chr3:179687940 | C | T | 40 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0109 others(37): Show |
41 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.295-2301C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179687940 | |||||||
chr3:179688079 | A | ATCCATCC others(13): Show |
2 | a0001c0002t0003g0158 a0001c0003t0001g0230 |
2 | HG01433.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.295-2147_295-2146i others(22): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688079 | ||||||
chr3:179688083 | A | ATCCATCC others(13): Show |
3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0005c0014t0001g0076 |
3 | NA18954.hp1 NA18999.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.295-2143_295-2142i others(22): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688083 | ||||||
chr3:179688083 | A | ATCCATCC others(9): Show |
6 | a0001c0001t0005g0202 a0001c0001t0005g0231 a0001c0001t0005g0232 others(3): Show |
6 | HG02055.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-2147_295-2146i others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688083 | ||||||
chr3:179688087 | A | ATCCATCC others(5): Show |
2 | a0001c0001t0006g0240 a0001c0002t0005g0171 |
2 | HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.295-2147_295-2146i others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688087 | ||||||
chr3:179688099 | G | A | 14 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0005g0202 others(11): Show |
14 | HG01433.hp1 HG02055.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.295-2142G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179688099 | |||||||
chr3:179688099 | G | GTCCA | 32 | a0001c0001t0001g0030 a0001c0001t0001g0109 a0001c0001t0001g0211 others(29): Show |
33 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.295-2112_295-2109d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688099 | ||||||
chr3:179688099 | G | GTCCATCC others(1): Show |
19 | a0001c0001t0001g0020 a0001c0001t0001g0115 a0001c0001t0001g0260 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.295-2116_295-2109d others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688099 | ||||||
chr3:179688099 | G | GTCCATCC others(5): Show |
96 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0032 others(93): Show |
96 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.295-2120_295-2109d others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688099 | ||||||
chr3:179688099 | G | GTCCATCC others(9): Show |
93 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0031 others(90): Show |
93 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.295-2124_295-2109d others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688099 | ||||||
chr3:179688099 | G | GTCCATCC others(13): Show |
12 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0052 others(9): Show |
12 | HG00597.hp1 HG00673.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-2128_295-2109d others(22): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688099 | ||||||
chr3:179688099 | G | GTCCGTCC others(13): Show |
1 | a0001c0001t0001g0121 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.295-2139_295-2138i others(22): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688099 | ||||||
chr3:179688138 | C | CATCCATC others(9): Show |
1 | a0001c0002t0001g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.295-2074_295-2059d others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688138 | ||||||
chr3:179688138 | CATCCATC others(9): Show |
C | 2 | a0001c0001t0007g0209 a0001c0004t0006g0107 |
2 | HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.295-2074_295-2059d others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688138 | ||||||
chr3:179688161 | C | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295-2080C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179688161 | |||||||
chr3:179688194 | A | AATCC | 23 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0005g0017 others(20): Show |
23 | HG00140.hp2 HG00323.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.295-2005_295-2002d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688194 | ||||||
chr3:179688234 | C | CATCCATC others(13): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0282 |
2 | HG03688.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.295-2002_295-2001i others(22): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688234 | ||||||
chr3:179688234 | C | CATCCATC others(9): Show |
28 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0080 others(25): Show |
28 | HG00597.hp2 HG00621.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.295-2002_295-2001i others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688234 | ||||||
chr3:179688234 | C | CATCCATC others(5): Show |
139 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0025 others(136): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.295-2002_295-2001i others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688234 | ||||||
chr3:179688234 | C | CATCCATC others(1): Show |
84 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0041 others(81): Show |
84 | HG00597.hp1 HG00673.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.295-2002_295-2001i others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 179688234 | ||||||
chr3:179688234 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.295-2007C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179688234 | |||||||
chr3:179688341 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0002g0085 a0001c0001t0002g0114 |
3 | NA18948.hp2 NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.295-1900C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179688341 | |||||||
chr3:179688417 | C | T | 40 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0109 others(37): Show |
41 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.295-1824C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179688417 | |||||||
chr3:179688483 | C | T | 2 | a0001c0002t0016g0173 a0001c0002t0033g0174 |
2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.295-1758C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179688483 | |||||||
chr3:179688809 | A | G | 53 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(50): Show |
53 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.295-1432A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179688809 | |||||||
chr3:179689154 | C | T | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.295-1087C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179689154 | |||||||
chr3:179689305 | T | C | 1 | a0001c0001t0008g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.295-936T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179689305 | |||||||
chr3:179689317 | G | A | 11 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0022g0257 others(8): Show |
11 | HG01109.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-924G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179689317 | |||||||
chr3:179689405 | G | T | 277 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(274): Show |
278 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.295-836G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179689405 | |||||||
chr3:179689424 | C | T | 54 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(51): Show |
54 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.295-817C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179689424 | |||||||
chr3:179689626 | C | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(45): Show |
48 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.295-615C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179689626 | |||||||
chr3:179689697 | A | G | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.295-544A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179689697 | |||||||
chr3:179690033 | T | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295-208T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179690033 | |||||||
chr3:179690043 | A | G | 27 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0005g0017 others(24): Show |
27 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.295-198A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179690043 | |||||||
chr3:179690222 | T | A | 2 | a0001c0009t0005g0238 a0001c0016t0004g0189 |
2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.295-19T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 2/20 | chr3 | 179690222 | |||||||
chr3:179690365 | T | C | 1 | a0001c0002t0001g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.355+64T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179690365 | |||||||
chr3:179690683 | C | T | 13 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0004t0002g0182 others(10): Show |
13 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.355+382C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179690683 | |||||||
chr3:179691153 | C | T | 4 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0002t0008g0164 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+852C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179691153 | |||||||
chr3:179691167 | TA | T | 242 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(239): Show |
242 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.355+883delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179691167 | ||||||
chr3:179691430 | C | G | 1 | a0001c0003t0001g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.355+1129C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179691430 | |||||||
chr3:179691850 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.355+1549G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179691850 | |||||||
chr3:179691884 | C | T | 16 | a0001c0001t0001g0025 a0001c0001t0003g0021 a0001c0001t0003g0022 others(13): Show |
16 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.355+1583C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179691884 | |||||||
chr3:179691952 | A | G | 1 | a0001c0003t0001g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.355+1651A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179691952 | |||||||
chr3:179692057 | A | C | 130 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0032 others(127): Show |
130 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.355+1756A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179692057 | |||||||
chr3:179692190 | C | T | 10 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0022g0257 others(7): Show |
10 | HG01109.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.355+1889C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179692190 | |||||||
chr3:179692191 | G | A | 1 | a0001c0001t0024g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.355+1890G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179692191 | |||||||
chr3:179692392 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.355+2091C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179692392 | |||||||
chr3:179692554 | A | G | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.355+2253A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179692554 | |||||||
chr3:179692613 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.355+2312T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179692613 | |||||||
chr3:179692908 | C | T | 1 | a0001c0003t0001g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.355+2607C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179692908 | |||||||
chr3:179692937 | G | T | 1 | a0001c0002t0002g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.355+2636G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179692937 | |||||||
chr3:179692975 | A | G | 4 | a0001c0001t0015g0292 a0001c0002t0004g0143 a0001c0002t0015g0130 others(1): Show |
4 | HG02055.hp2 HG02257.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+2674A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179692975 | |||||||
chr3:179693039 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.355+2738A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179693039 | |||||||
chr3:179693326 | T | A | 4 | a0001c0001t0007g0268 a0001c0002t0007g0001 a0001c0002t0007g0168 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+3025T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179693326 | |||||||
chr3:179693331 | T | C | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.355+3030T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179693331 | |||||||
chr3:179693456 | A | G | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.355+3155A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179693456 | |||||||
chr3:179693761 | C | T | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.355+3460C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179693761 | |||||||
chr3:179693799 | G | A | 53 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(50): Show |
53 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.355+3498G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179693799 | |||||||
chr3:179694123 | G | T | 42 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(39): Show |
42 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.355+3822G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694123 | |||||||
chr3:179694216 | C | A | 4 | a0001c0003t0039g0019 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+3915C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694216 | |||||||
chr3:179694270 | C | T | 5 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0002t0008g0164 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+3969C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694270 | |||||||
chr3:179694279 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.355+3978C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694279 | |||||||
chr3:179694304 | C | T | 53 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(50): Show |
53 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.355+4003C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694304 | |||||||
chr3:179694462 | G | T | 4 | a0001c0003t0039g0019 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+4161G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694462 | |||||||
chr3:179694541 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.355+4240G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694541 | |||||||
chr3:179694732 | C | T | 1 | a0001c0001t0003g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.355+4431C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694732 | |||||||
chr3:179694736 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.355+4435G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694736 | |||||||
chr3:179694756 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.355+4455G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694756 | |||||||
chr3:179694782 | A | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0031 others(98): Show |
101 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.355+4481A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694782 | |||||||
chr3:179694799 | CAAA | C | 90 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0031 others(87): Show |
90 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.355+4520_355+4522d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179694799 | ||||||
chr3:179694799 | CAAAA | C | 9 | a0001c0001t0001g0205 a0001c0001t0001g0287 a0001c0001t0019g0204 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.355+4519_355+4522d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179694799 | ||||||
chr3:179694799 | CAAAAAAA others(7): Show |
C | 1 | a0001c0008t0004g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355+4509_355+4522d others(16): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179694799 | ||||||
chr3:179694801 | A | AAG | 6 | a0001c0001t0003g0087 a0001c0003t0001g0255 a0001c0006t0002g0138 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.355+4501_355+4502i others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179694801 | ||||||
chr3:179694802 | A | AG | 123 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0032 others(120): Show |
123 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.355+4501_355+4502i others(3): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694802 | |||||||
chr3:179694803 | A | G | 3 | a0001c0001t0004g0261 a0001c0002t0001g0135 a0001c0002t0042g0129 |
3 | HG01069.hp1 HG02970.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.355+4502A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694803 | |||||||
chr3:179694809 | A | G | 1 | a0001c0002t0002g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.355+4508A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179694809 | |||||||
chr3:179695006 | C | T | 53 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(50): Show |
53 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.355+4705C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179695006 | |||||||
chr3:179695007 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.355+4706G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179695007 | |||||||
chr3:179695533 | A | AT | 11 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0022g0257 others(8): Show |
11 | HG01109.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.355+5245dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179695533 | ||||||
chr3:179695766 | C | T | 53 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(50): Show |
53 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.356-5242C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179695766 | |||||||
chr3:179695797 | G | A | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.356-5211G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179695797 | |||||||
chr3:179695846 | C | T | 10 | a0001c0001t0005g0202 a0001c0001t0005g0231 a0001c0001t0005g0232 others(7): Show |
10 | HG01433.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.356-5162C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179695846 | |||||||
chr3:179696081 | A | C | 1 | a0001c0005t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.356-4927A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696081 | |||||||
chr3:179696098 | A | C | 1 | a0001c0003t0001g0290 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.356-4910A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696098 | |||||||
chr3:179696132 | G | A | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.356-4876G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696132 | |||||||
chr3:179696196 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-4812C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696196 | |||||||
chr3:179696328 | A | AT | 38 | a0001c0001t0001g0082 a0001c0001t0001g0219 a0001c0001t0001g0222 others(35): Show |
38 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.356-4661dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179696328 | ||||||
chr3:179696328 | A | ATT | 182 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0027 others(179): Show |
183 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.356-4662_356-4661d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179696328 | ||||||
chr3:179696328 | A | ATTT | 54 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(51): Show |
54 | HG00280.hp2 HG00558.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.356-4663_356-4661d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179696328 | ||||||
chr3:179696351 | A | T | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.356-4657A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696351 | |||||||
chr3:179696412 | C | T | 24 | a0001c0001t0002g0007 a0001c0001t0002g0097 a0001c0001t0005g0017 others(21): Show |
24 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.356-4596C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696412 | |||||||
chr3:179696501 | T | G | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.356-4507T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696501 | |||||||
chr3:179696522 | G | A | 39 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(36): Show |
39 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.356-4486G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696522 | |||||||
chr3:179696780 | G | T | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.356-4228G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696780 | |||||||
chr3:179696917 | G | A | 237 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(234): Show |
237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.356-4091G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179696917 | |||||||
chr3:179697209 | G | T | 2 | a0001c0001t0012g0070 a0001c0001t0012g0113 |
2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.356-3799G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179697209 | |||||||
chr3:179697565 | T | C | 4 | a0001c0004t0034g0072 a0001c0006t0004g0179 a0001c0006t0006g0181 others(1): Show |
4 | HG03195.hp1 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-3443T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179697565 | |||||||
chr3:179697681 | T | C | 24 | a0001c0001t0002g0007 a0001c0001t0005g0017 a0001c0001t0006g0297 others(21): Show |
24 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.356-3327T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179697681 | |||||||
chr3:179697807 | G | A | 54 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(51): Show |
54 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.356-3201G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179697807 | |||||||
chr3:179697824 | G | T | 1 | a0001c0008t0004g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.356-3184G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179697824 | |||||||
chr3:179697847 | C | T | 3 | a0001c0001t0001g0205 a0001c0001t0019g0204 a0001c0001t0021g0295 |
3 | HG06807.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.356-3161C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179697847 | |||||||
chr3:179697986 | A | G | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.356-3022A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179697986 | |||||||
chr3:179698212 | C | A | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.356-2796C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179698212 | |||||||
chr3:179698346 | C | A | 27 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(24): Show |
27 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.356-2662C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179698346 | |||||||
chr3:179698423 | A | G | 1 | a0001c0002t0043g0125 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.356-2585A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179698423 | |||||||
chr3:179698494 | G | T | 71 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(68): Show |
71 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.356-2514G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179698494 | |||||||
chr3:179698514 | A | T | 237 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(234): Show |
237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.356-2494A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179698514 | |||||||
chr3:179698540 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.356-2468T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179698540 | |||||||
chr3:179698825 | G | C | 34 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(31): Show |
34 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(31): Show |
intron_variant | MODIFIER | c.356-2183G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179698825 | |||||||
chr3:179698871 | A | AT | 171 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(168): Show |
171 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.356-2123dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179698871 | ||||||
chr3:179699001 | T | C | 3 | a0001c0001t0006g0297 a0001c0002t0004g0170 a0001c0002t0006g0169 |
3 | HG01109.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.356-2007T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699001 | |||||||
chr3:179699016 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.356-1992G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699016 | |||||||
chr3:179699164 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.356-1844C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699164 | |||||||
chr3:179699430 | A | G | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.356-1578A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699430 | |||||||
chr3:179699585 | A | T | 1 | a0001c0002t0009g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.356-1423A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699585 | |||||||
chr3:179699586 | G | C | 2 | a0001c0001t0002g0012 a0001c0002t0009g0160 |
2 | HG01081.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.356-1422G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699586 | |||||||
chr3:179699691 | C | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0094 a0001c0001t0001g0121 others(5): Show |
8 | HG00621.hp2 HG02165.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.356-1317C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699691 | |||||||
chr3:179699699 | C | CA | 59 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(56): Show |
60 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.356-1294dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699699 | ||||||
chr3:179699699 | C | CAAA | 149 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(146): Show |
149 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.356-1296_356-1294d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699699 | ||||||
chr3:179699699 | C | CAAAA | 21 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0008g0293 others(18): Show |
21 | HG01109.hp1 HG01109.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.356-1297_356-1294d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699699 | ||||||
chr3:179699699 | C | CAAAAA | 10 | a0001c0001t0002g0007 a0001c0004t0002g0182 a0001c0004t0002g0267 others(7): Show |
10 | HG00140.hp2 HG01099.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.356-1298_356-1294d others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699699 | ||||||
chr3:179699699 | CA | C | 6 | a0001c0001t0007g0241 a0001c0001t0010g0193 a0001c0001t0010g0194 others(3): Show |
6 | HG01978.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.356-1294delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699699 | ||||||
chr3:179699739 | C | CTTATT | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0015g0292 |
3 | HG00738.hp1 HG02717.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.356-1267_356-1263d others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699739 | ||||||
chr3:179699739 | CTTAT | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0246 a0001c0001t0019g0204 others(1): Show |
4 | HG02080.hp2 HG06807.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-1262_356-1259d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699739 | ||||||
chr3:179699742 | A | AT | 11 | a0001c0001t0001g0055 a0001c0001t0001g0092 a0001c0001t0002g0077 others(8): Show |
11 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.356-1263dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699742 | ||||||
chr3:179699746 | A | T | 18 | a0001c0001t0001g0050 a0001c0001t0001g0248 a0001c0001t0002g0003 others(15): Show |
18 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.356-1262A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699746 | |||||||
chr3:179699747 | T | A | 18 | a0001c0001t0001g0050 a0001c0001t0001g0248 a0001c0001t0002g0003 others(15): Show |
18 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.356-1261T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699747 | |||||||
chr3:179699747 | T | TTTA | 14 | a0001c0001t0001g0055 a0001c0001t0001g0092 a0001c0001t0001g0095 others(11): Show |
14 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.356-1259_356-1258i others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699747 | ||||||
chr3:179699747 | T | TTTTA | 38 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0053 others(35): Show |
38 | HG00323.hp1 HG00673.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.356-1221_356-1218d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699747 | ||||||
chr3:179699747 | T | TTTTATTT others(1): Show |
22 | a0001c0001t0001g0025 a0001c0001t0001g0221 a0001c0001t0003g0021 others(19): Show |
22 | HG00140.hp2 HG01255.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.356-1225_356-1218d others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699747 | ||||||
chr3:179699747 | TTTTA | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0039 others(62): Show |
66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.356-1221_356-1218d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699747 | ||||||
chr3:179699747 | TTTTATTT others(1): Show |
T | 19 | a0001c0001t0001g0034 a0001c0001t0001g0063 a0001c0001t0001g0080 others(16): Show |
19 | HG00642.hp2 HG01169.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.356-1225_356-1218d others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699747 | ||||||
chr3:179699747 | TTTTATTT others(5): Show |
T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0287 others(4): Show |
7 | HG00558.hp2 HG01109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-1229_356-1218d others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699747 | ||||||
chr3:179699747 | TTTTATTT others(9): Show |
T | 10 | a0001c0001t0001g0222 a0001c0001t0002g0014 a0001c0001t0002g0024 others(7): Show |
10 | HG00140.hp1 HG01257.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.356-1233_356-1218d others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179699747 | ||||||
chr3:179699750 | T | A | 1 | a0001c0001t0001g0284 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.356-1258T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699750 | |||||||
chr3:179699751 | A | T | 1 | a0001c0001t0001g0284 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.356-1257A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699751 | |||||||
chr3:179699878 | A | T | 1 | a0001c0001t0037g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.356-1130A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699878 | |||||||
chr3:179699970 | G | A | 1 | a0001c0003t0001g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.356-1038G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179699970 | |||||||
chr3:179700188 | C | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(238): Show |
241 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.356-820C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179700188 | |||||||
chr3:179700375 | T | C | 2 | a0001c0001t0014g0184 a0001c0011t0025g0183 |
2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.356-633T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179700375 | |||||||
chr3:179700429 | A | C | 55 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(52): Show |
55 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.356-579A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179700429 | |||||||
chr3:179700611 | T | A | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.356-397T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179700611 | |||||||
chr3:179700668 | T | C | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.356-340T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179700668 | |||||||
chr3:179700787 | A | G | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.356-221A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179700787 | |||||||
chr3:179700912 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-96C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | chr3 | 179700912 | |||||||
chr3:179700975 | ACTT | A | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.356-29_356-27delCT others(1): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 179700975 | ||||||
chr3:179701387 | T | C | 232 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(229): Show |
232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.477+258T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701387 | |||||||
chr3:179701435 | G | T | 1 | a0001c0002t0001g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.477+306G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701435 | |||||||
chr3:179701474 | G | A | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.477+345G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701474 | |||||||
chr3:179701572 | A | C | 1 | a0001c0001t0001g0031 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.477+443A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701572 | |||||||
chr3:179701645 | C | T | 1 | a0001c0002t0009g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.477+516C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701645 | |||||||
chr3:179701765 | C | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(45): Show |
48 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.477+636C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701765 | |||||||
chr3:179701790 | A | T | 26 | a0001c0001t0004g0261 a0001c0001t0005g0017 a0001c0001t0006g0297 others(23): Show |
26 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.477+661A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701790 | |||||||
chr3:179701810 | C | G | 74 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(71): Show |
74 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.477+681C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701810 | |||||||
chr3:179701924 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.477+795G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701924 | |||||||
chr3:179701944 | T | G | 25 | a0001c0001t0004g0206 a0001c0001t0004g0261 a0001c0001t0006g0297 others(22): Show |
25 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.477+815T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701944 | |||||||
chr3:179701984 | T | C | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.477+855T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179701984 | |||||||
chr3:179702034 | T | C | 26 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(23): Show |
26 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.477+905T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702034 | |||||||
chr3:179702058 | T | C | 54 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(51): Show |
54 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.477+929T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702058 | |||||||
chr3:179702124 | G | A | 4 | a0001c0001t0001g0218 a0001c0009t0005g0238 a0001c0009t0005g0291 others(1): Show |
4 | HG00597.hp2 HG01891.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+995G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702124 | |||||||
chr3:179702173 | T | C | 235 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(232): Show |
235 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.477+1044T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702173 | |||||||
chr3:179702177 | G | A | 54 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(51): Show |
54 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.477+1048G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702177 | |||||||
chr3:179702178 | C | T | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.477+1049C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702178 | |||||||
chr3:179702186 | T | A | 230 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(227): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.477+1057T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702186 | |||||||
chr3:179702315 | G | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(77): Show |
80 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.477+1186G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702315 | |||||||
chr3:179702397 | C | G | 1 | a0001c0001t0001g0006 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.477+1268C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702397 | |||||||
chr3:179702583 | C | A | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.477+1454C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702583 | |||||||
chr3:179702602 | C | T | 114 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0041 others(111): Show |
114 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.477+1473C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702602 | |||||||
chr3:179702654 | G | A | 73 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(70): Show |
73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.477+1525G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702654 | |||||||
chr3:179702656 | G | A | 113 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0041 others(110): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.477+1527G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702656 | |||||||
chr3:179702656 | G | C | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.477+1527G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702656 | |||||||
chr3:179702763 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0019g0204 a0001c0001t0021g0295 |
3 | HG06807.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.477+1634G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702763 | |||||||
chr3:179702803 | C | T | 23 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0008g0293 others(20): Show |
23 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.477+1674C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702803 | |||||||
chr3:179702877 | G | A | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.477+1748G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702877 | |||||||
chr3:179702878 | T | G | 73 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(70): Show |
73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.477+1749T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179702878 | |||||||
chr3:179703101 | C | A | 1 | a0001c0001t0012g0070 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.477+1972C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703101 | |||||||
chr3:179703302 | G | A | 1 | a0001c0004t0006g0226 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.477+2173G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703302 | |||||||
chr3:179703505 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.477+2376G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703505 | |||||||
chr3:179703548 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.477+2419G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703548 | |||||||
chr3:179703681 | C | T | 11 | a0001c0004t0002g0182 a0001c0004t0002g0267 a0001c0004t0006g0107 others(8): Show |
11 | HG00140.hp2 HG01099.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.477+2552C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703681 | |||||||
chr3:179703716 | T | C | 54 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(51): Show |
54 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.477+2587T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703716 | |||||||
chr3:179703759 | A | G | 55 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(52): Show |
55 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.477+2630A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703759 | |||||||
chr3:179703888 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.477+2759C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703888 | |||||||
chr3:179703889 | G | A | 2 | a0001c0001t0002g0097 a0001c0002t0002g0162 |
2 | HG00323.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.477+2760G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703889 | |||||||
chr3:179703943 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0109 others(3): Show |
6 | HG00558.hp2 HG02015.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+2814G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179703943 | |||||||
chr3:179704002 | C | T | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.477+2873C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704002 | |||||||
chr3:179704003 | A | G | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.477+2874A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704003 | |||||||
chr3:179704009 | A | T | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.477+2880A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704009 | |||||||
chr3:179704314 | A | C | 1 | a0001c0002t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.478-2620A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704314 | |||||||
chr3:179704497 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.478-2437C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704497 | |||||||
chr3:179704552 | G | A | 23 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0008g0293 others(20): Show |
23 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.478-2382G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704552 | |||||||
chr3:179704568 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.478-2366T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704568 | |||||||
chr3:179704667 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0117 |
2 | HG02129.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.478-2267A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704667 | |||||||
chr3:179704806 | C | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(42): Show |
45 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.478-2128C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704806 | |||||||
chr3:179704951 | C | T | 1 | a0001c0001t0003g0296 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.478-1983C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704951 | |||||||
chr3:179704969 | T | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(75): Show |
78 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.478-1965T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704969 | |||||||
chr3:179704982 | G | A | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.478-1952G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704982 | |||||||
chr3:179704989 | G | A | 2 | a0001c0001t0008g0198 a0001c0001t0027g0199 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.478-1945G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179704989 | |||||||
chr3:179705009 | G | T | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.478-1925G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705009 | |||||||
chr3:179705013 | C | T | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.478-1921C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705013 | |||||||
chr3:179705072 | G | T | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.478-1862G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705072 | |||||||
chr3:179705194 | A | G | 4 | a0001c0003t0039g0019 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-1740A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705194 | |||||||
chr3:179705308 | AT | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0094 a0001c0001t0001g0121 others(5): Show |
8 | HG00621.hp2 HG02165.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1623delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 179705308 | ||||||
chr3:179705496 | C | G | 11 | a0001c0004t0002g0182 a0001c0004t0002g0267 a0001c0004t0006g0107 others(8): Show |
11 | HG00140.hp2 HG01099.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.478-1438C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705496 | |||||||
chr3:179705645 | A | G | 73 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(70): Show |
73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.478-1289A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705645 | |||||||
chr3:179705720 | T | TA | 4 | a0001c0003t0039g0019 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-1213dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 179705720 | ||||||
chr3:179705731 | T | A | 11 | a0001c0004t0002g0182 a0001c0004t0002g0267 a0001c0004t0006g0107 others(8): Show |
11 | HG00140.hp2 HG01099.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.478-1203T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705731 | |||||||
chr3:179705781 | G | A | 54 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(51): Show |
54 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.478-1153G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705781 | |||||||
chr3:179705847 | T | C | 231 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(228): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.478-1087T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705847 | |||||||
chr3:179705947 | T | C | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.478-987T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179705947 | |||||||
chr3:179706078 | T | C | 1 | a0001c0001t0014g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.478-856T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179706078 | |||||||
chr3:179706108 | ATATAT | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(42): Show |
45 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.478-825_478-821del others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179706108 | |||||||
chr3:179706114 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(42): Show |
45 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.478-820A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179706114 | |||||||
chr3:179706138 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.478-796T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179706138 | |||||||
chr3:179706270 | A | C | 239 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(236): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.478-664A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179706270 | |||||||
chr3:179706302 | A | G | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478-632A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179706302 | |||||||
chr3:179706449 | C | A | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478-485C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179706449 | |||||||
chr3:179706622 | G | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(42): Show |
45 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.478-312G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 4/20 | chr3 | 179706622 | |||||||
chr3:179707231 | C | T | 4 | a0001c0003t0039g0019 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+155C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707231 | |||||||
chr3:179707281 | T | C | 54 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(51): Show |
54 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.620+205T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707281 | |||||||
chr3:179707303 | AGCACTTG others(9): Show |
A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(42): Show |
45 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.620+231_620+246del others(16): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 179707303 | ||||||
chr3:179707359 | A | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(174): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.620+283A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707359 | |||||||
chr3:179707413 | C | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(42): Show |
45 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.620+337C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707413 | |||||||
chr3:179707424 | C | T | 3 | a0001c0009t0005g0238 a0001c0009t0005g0291 a0001c0016t0004g0189 |
3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.620+348C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707424 | |||||||
chr3:179707467 | C | T | 4 | a0001c0001t0002g0216 a0001c0001t0002g0223 a0001c0001t0035g0056 others(1): Show |
4 | NA18945.hp1 NA18949.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+391C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707467 | |||||||
chr3:179707545 | T | C | 73 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(70): Show |
73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.620+469T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707545 | |||||||
chr3:179707663 | A | C | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.620+587A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707663 | |||||||
chr3:179707724 | A | G | 73 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(70): Show |
73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.620+648A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707724 | |||||||
chr3:179707967 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.621-806G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179707967 | |||||||
chr3:179708020 | T | C | 4 | a0001c0003t0039g0019 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.621-753T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179708020 | |||||||
chr3:179708034 | A | C | 23 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0008g0293 others(20): Show |
23 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.621-739A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179708034 | |||||||
chr3:179708109 | T | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(45): Show |
48 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.621-664T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179708109 | |||||||
chr3:179708171 | A | G | 145 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(142): Show |
145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.621-602A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179708171 | |||||||
chr3:179708288 | G | A | 286 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(283): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.621-485G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179708288 | |||||||
chr3:179708308 | AT | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(138): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.621-449delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 179708308 | ||||||
chr3:179708337 | T | C | 1 | a0001c0003t0001g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.621-436T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179708337 | |||||||
chr3:179708439 | CTGGGATT | C | 180 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(177): Show |
180 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.621-326_621-320del others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 179708439 | ||||||
chr3:179708503 | C | T | 6 | a0001c0003t0001g0230 a0001c0003t0005g0002 a0001c0003t0005g0242 others(3): Show |
6 | HG01433.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.621-270C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179708503 | |||||||
chr3:179708524 | C | T | 4 | a0001c0001t0017g0192 a0001c0009t0005g0238 a0001c0009t0005g0291 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.621-249C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179708524 | |||||||
chr3:179708595 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.621-178C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 5/20 | chr3 | 179708595 | |||||||
chr3:179708967 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.805+10C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179708967 | |||||||
chr3:179709199 | T | C | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.805+242T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709199 | |||||||
chr3:179709436 | G | T | 1 | a0001c0002t0004g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.805+479G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709436 | |||||||
chr3:179709446 | A | C | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.805+489A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709446 | |||||||
chr3:179709674 | A | T | 1 | a0001c0016t0004g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.805+717A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709674 | |||||||
chr3:179709687 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.805+730G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709687 | |||||||
chr3:179709688 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.805+731G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709688 | |||||||
chr3:179709689 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.805+732C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709689 | |||||||
chr3:179709713 | T | C | 4 | a0001c0001t0007g0268 a0001c0002t0007g0001 a0001c0002t0007g0168 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+756T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709713 | |||||||
chr3:179709934 | A | G | 6 | a0001c0002t0004g0172 a0001c0002t0004g0187 a0001c0002t0004g0270 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.805+977A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709934 | |||||||
chr3:179709981 | GTA | G | 71 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(68): Show |
71 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.805+1025_805+1026d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179709981 | |||||||
chr3:179710195 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0275 |
2 | HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.805+1238C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179710195 | |||||||
chr3:179710345 | A | G | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.805+1388A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179710345 | |||||||
chr3:179710420 | A | T | 88 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(85): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.805+1463A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179710420 | |||||||
chr3:179710642 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(78): Show |
81 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.805+1685T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179710642 | |||||||
chr3:179710663 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.805+1706T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179710663 | |||||||
chr3:179710668 | C | T | 185 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(182): Show |
185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.805+1711C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179710668 | |||||||
chr3:179710914 | T | A | 6 | a0001c0001t0007g0241 a0001c0001t0010g0193 a0001c0001t0010g0194 others(3): Show |
6 | HG01978.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.805+1957T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179710914 | |||||||
chr3:179711032 | C | T | 1 | a0001c0002t0004g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.805+2075C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711032 | |||||||
chr3:179711159 | A | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(78): Show |
81 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.805+2202A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711159 | |||||||
chr3:179711218 | T | A | 54 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(51): Show |
54 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.805+2261T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711218 | |||||||
chr3:179711314 | A | G | 1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.805+2357A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711314 | |||||||
chr3:179711376 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.805+2419G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711376 | |||||||
chr3:179711525 | A | T | 16 | a0001c0001t0004g0206 a0001c0001t0005g0017 a0001c0001t0006g0297 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.805+2568A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711525 | |||||||
chr3:179711580 | T | C | 1 | a0001c0001t0007g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.805+2623T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711580 | |||||||
chr3:179711592 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.805+2635T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711592 | |||||||
chr3:179711632 | T | A | 16 | a0001c0001t0004g0206 a0001c0001t0005g0017 a0001c0001t0006g0297 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.805+2675T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711632 | |||||||
chr3:179711799 | G | A | 1 | a0001c0001t0008g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.805+2842G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179711799 | |||||||
chr3:179712009 | T | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0089 |
2 | NA18995.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.805+3052T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179712009 | |||||||
chr3:179712240 | T | C | 16 | a0001c0001t0004g0206 a0001c0001t0005g0017 a0001c0001t0006g0297 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.805+3283T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179712240 | |||||||
chr3:179712257 | G | A | 1 | a0001c0008t0008g0265 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.805+3300G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179712257 | |||||||
chr3:179712365 | A | C | 1 | a0001c0002t0009g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.805+3408A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179712365 | |||||||
chr3:179712368 | A | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(78): Show |
81 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.805+3411A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179712368 | |||||||
chr3:179712489 | C | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0034 others(44): Show |
47 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.805+3532C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179712489 | |||||||
chr3:179712616 | C | G | 1 | a0001c0002t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.805+3659C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179712616 | |||||||
chr3:179712658 | T | C | 12 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(9): Show |
12 | HG00140.hp2 HG01099.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.805+3701T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179712658 | |||||||
chr3:179712690 | A | C | 1 | a0001c0002t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.805+3733A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179712690 | |||||||
chr3:179713153 | G | A | 239 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(236): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.805+4196G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179713153 | |||||||
chr3:179713206 | C | T | 1 | a0001c0001t0009g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.805+4249C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179713206 | |||||||
chr3:179713293 | CAG | C | 3 | a0001c0001t0002g0097 a0001c0002t0001g0163 a0001c0002t0002g0162 |
3 | HG00323.hp1 HG01074.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.805+4339_805+4340d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 179713293 | ||||||
chr3:179713501 | C | G | 1 | a0001c0001t0001g0286 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.805+4544C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179713501 | |||||||
chr3:179713507 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.805+4550G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179713507 | |||||||
chr3:179713588 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.805+4631C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179713588 | |||||||
chr3:179713810 | T | C | 2 | a0001c0002t0001g0154 a0001c0002t0001g0161 |
2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.805+4853T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179713810 | |||||||
chr3:179714123 | C | T | 6 | a0001c0003t0001g0230 a0001c0003t0005g0002 a0001c0003t0005g0242 others(3): Show |
6 | HG01433.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.805+5166C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179714123 | |||||||
chr3:179714174 | G | A | 88 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(85): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.805+5217G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179714174 | |||||||
chr3:179714316 | C | T | 12 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(9): Show |
12 | HG00140.hp2 HG01099.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.805+5359C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179714316 | |||||||
chr3:179714407 | G | A | 3 | a0001c0001t0008g0040 a0001c0002t0008g0164 a0001c0002t0008g0165 |
3 | HG01070.hp1 HG01071.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.805+5450G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179714407 | |||||||
chr3:179714541 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.806-5399A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179714541 | |||||||
chr3:179714870 | C | CT | 157 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0043 others(154): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.806-5056dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 179714870 | ||||||
chr3:179714870 | C | CTT | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(78): Show |
81 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.806-5057_806-5056d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 179714870 | ||||||
chr3:179715168 | C | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(78): Show |
81 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.806-4772C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715168 | |||||||
chr3:179715175 | C | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0066 a0001c0001t0002g0054 others(4): Show |
7 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.806-4765C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715175 | |||||||
chr3:179715191 | C | G | 1 | a0001c0009t0005g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.806-4749C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715191 | |||||||
chr3:179715367 | C | CT | 14 | a0001c0001t0001g0229 a0001c0001t0002g0003 a0001c0001t0002g0117 others(11): Show |
14 | HG00140.hp2 HG01099.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.806-4558dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 179715367 | ||||||
chr3:179715367 | C | CTT | 70 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(67): Show |
70 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.806-4559_806-4558d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 179715367 | ||||||
chr3:179715371 | T | C | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.806-4569T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715371 | |||||||
chr3:179715372 | T | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(44): Show |
47 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.806-4568T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715372 | |||||||
chr3:179715383 | G | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(44): Show |
47 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.806-4557G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715383 | |||||||
chr3:179715401 | C | G | 185 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(182): Show |
185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.806-4539C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715401 | |||||||
chr3:179715403 | G | A | 185 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(182): Show |
185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.806-4537G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715403 | |||||||
chr3:179715522 | G | A | 16 | a0001c0001t0004g0206 a0001c0001t0005g0017 a0001c0001t0006g0297 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.806-4418G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715522 | |||||||
chr3:179715692 | G | A | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.806-4248G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715692 | |||||||
chr3:179715807 | G | A | 2 | a0001c0001t0006g0035 a0001c0002t0006g0157 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.806-4133G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715807 | |||||||
chr3:179715857 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.806-4083C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715857 | |||||||
chr3:179715978 | G | A | 1 | a0001c0001t0006g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.806-3962G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179715978 | |||||||
chr3:179716112 | C | T | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.806-3828C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179716112 | |||||||
chr3:179716244 | G | T | 12 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0022g0257 others(9): Show |
12 | HG01109.hp1 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.806-3696G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179716244 | |||||||
chr3:179716364 | A | C | 4 | a0001c0004t0034g0072 a0001c0006t0004g0179 a0001c0006t0006g0181 others(1): Show |
4 | HG03195.hp1 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.806-3576A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179716364 | |||||||
chr3:179716382 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.806-3558T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179716382 | |||||||
chr3:179716452 | C | T | 1 | a0001c0008t0004g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.806-3488C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179716452 | |||||||
chr3:179716489 | C | G | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.806-3451C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179716489 | |||||||
chr3:179716566 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0003g0210 |
2 | HG02132.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.806-3374C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179716566 | |||||||
chr3:179716582 | T | C | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.806-3358T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179716582 | |||||||
chr3:179717007 | A | G | 5 | a0001c0002t0001g0134 a0001c0004t0034g0072 a0001c0006t0004g0179 others(2): Show |
5 | HG03195.hp1 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.806-2933A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717007 | |||||||
chr3:179717010 | C | G | 2 | a0001c0002t0001g0154 a0001c0002t0001g0161 |
2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.806-2930C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717010 | |||||||
chr3:179717099 | C | T | 25 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.806-2841C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717099 | |||||||
chr3:179717262 | C | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(94): Show |
97 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.806-2678C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717262 | |||||||
chr3:179717274 | G | C | 1 | a0001c0001t0002g0085 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.806-2666G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717274 | |||||||
chr3:179717341 | G | T | 3 | a0001c0001t0015g0292 a0001c0002t0015g0130 a0001c0003t0001g0239 |
3 | HG02055.hp2 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.806-2599G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717341 | |||||||
chr3:179717344 | T | A | 1 | a0001c0001t0001g0254 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.806-2596T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717344 | |||||||
chr3:179717595 | C | A | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.806-2345C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717595 | |||||||
chr3:179717670 | T | TC | 239 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(236): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.806-2270_806-2269i others(3): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717670 | |||||||
chr3:179717671 | G | C | 239 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(236): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.806-2269G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717671 | |||||||
chr3:179717742 | A | G | 1 | a0001c0002t0009g0141 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.806-2198A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179717742 | |||||||
chr3:179717956 | T | TAGAA | 239 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(236): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.806-1981_806-1980i others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 179717956 | ||||||
chr3:179718286 | C | CT | 227 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(224): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.806-1642dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 179718286 | ||||||
chr3:179718510 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(94): Show |
97 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.806-1430C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179718510 | |||||||
chr3:179718607 | T | C | 4 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0002t0008g0164 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-1333T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179718607 | |||||||
chr3:179718696 | A | G | 186 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(183): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.806-1244A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179718696 | |||||||
chr3:179718807 | A | T | 5 | a0001c0002t0001g0134 a0001c0004t0034g0072 a0001c0006t0004g0179 others(2): Show |
5 | HG03195.hp1 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.806-1133A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179718807 | |||||||
chr3:179718849 | T | C | 12 | a0001c0001t0005g0017 a0001c0001t0006g0297 a0001c0001t0022g0257 others(9): Show |
12 | HG01109.hp1 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.806-1091T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179718849 | |||||||
chr3:179718874 | AGCCTCCC others(10): Show |
A | 4 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0002t0008g0164 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-1064_806-1048d others(19): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 179718874 | ||||||
chr3:179719328 | G | A | 2 | a0001c0004t0002g0267 a0001c0006t0002g0138 |
2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.806-612G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179719328 | |||||||
chr3:179719422 | C | T | 16 | a0001c0001t0004g0206 a0001c0001t0005g0017 a0001c0001t0006g0297 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.806-518C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179719422 | |||||||
chr3:179719622 | A | G | 1 | a0001c0009t0005g0291 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.806-318A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179719622 | |||||||
chr3:179719643 | T | C | 4 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0002t0008g0164 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-297T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179719643 | |||||||
chr3:179719749 | A | G | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.806-191A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179719749 | |||||||
chr3:179719834 | G | A | 4 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0002t0008g0164 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-106G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 6/20 | chr3 | 179719834 | |||||||
chr3:179720148 | T | C | 5 | a0001c0002t0001g0134 a0001c0004t0034g0072 a0001c0006t0004g0179 others(2): Show |
5 | HG03195.hp1 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.900+114T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720148 | |||||||
chr3:179720174 | A | G | 1 | a0001c0001t0028g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.900+140A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720174 | |||||||
chr3:179720183 | T | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(84): Show |
87 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.900+149T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720183 | |||||||
chr3:179720198 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(42): Show |
45 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.900+164A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720198 | |||||||
chr3:179720313 | G | A | 16 | a0001c0001t0004g0206 a0001c0001t0005g0017 a0001c0001t0006g0297 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.900+279G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720313 | |||||||
chr3:179720341 | G | A | 4 | a0001c0001t0014g0184 a0001c0001t0014g0276 a0001c0001t0030g0258 others(1): Show |
4 | HG02145.hp2 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.900+307G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720341 | |||||||
chr3:179720438 | T | C | 195 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(192): Show |
195 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.900+404T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720438 | |||||||
chr3:179720528 | A | G | 3 | a0001c0001t0006g0073 a0001c0001t0006g0116 a0001c0001t0006g0228 |
3 | HG02602.hp2 HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.900+494A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720528 | |||||||
chr3:179720559 | G | A | 276 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(273): Show |
277 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.900+525G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720559 | |||||||
chr3:179720563 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0280 |
2 | HG00597.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.900+529C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720563 | |||||||
chr3:179720581 | C | T | 2 | a0001c0002t0008g0164 a0001c0002t0008g0165 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.900+547C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720581 | |||||||
chr3:179720676 | C | T | 1 | a0001c0002t0004g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.900+642C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720676 | |||||||
chr3:179720776 | A | G | 1 | a0001c0001t0004g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.901-626A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720776 | |||||||
chr3:179720811 | C | CT | 28 | a0001c0001t0001g0064 a0001c0001t0001g0111 a0001c0001t0004g0206 others(25): Show |
28 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.901-577dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 179720811 | ||||||
chr3:179720871 | C | T | 2 | a0001c0006t0006g0181 a0001c0006t0032g0140 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.901-531C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179720871 | |||||||
chr3:179721075 | T | C | 248 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(245): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.901-327T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179721075 | |||||||
chr3:179721215 | T | C | 2 | a0001c0001t0004g0105 a0001c0001t0004g0236 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.901-187T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | chr3 | 179721215 | |||||||
chr3:179721256 | CTT | C | 4 | a0001c0003t0001g0255 a0001c0009t0005g0238 a0001c0009t0005g0291 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.901-141_901-140del others(2): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 179721256 | ||||||
chr3:179721621 | G | A | 1 | a0001c0001t0028g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1088+32G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179721621 | |||||||
chr3:179721678 | T | C | 81 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1088+89T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179721678 | |||||||
chr3:179721748 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(85): Show |
88 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.1088+159G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179721748 | |||||||
chr3:179721763 | G | T | 1 | a0001c0001t0006g0081 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1088+174G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179721763 | |||||||
chr3:179721779 | A | G | 81 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1088+190A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179721779 | |||||||
chr3:179721875 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0278 |
2 | HG01952.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1088+286G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179721875 | |||||||
chr3:179721890 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1088+301C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179721890 | |||||||
chr3:179722003 | T | C | 2 | a0001c0001t0014g0184 a0001c0001t0014g0276 |
2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1088+414T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722003 | |||||||
chr3:179722065 | C | CA | 98 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(95): Show |
99 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.1088+493dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179722065 | ||||||
chr3:179722065 | CAAA | C | 80 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1088+491_1088+493d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179722065 | ||||||
chr3:179722083 | G | A | 1 | a0001c0002t0009g0141 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1088+494G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722083 | |||||||
chr3:179722091 | T | C | 2 | a0001c0001t0008g0198 a0001c0001t0027g0199 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1088+502T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722091 | |||||||
chr3:179722154 | C | T | 3 | a0001c0002t0001g0134 a0001c0004t0034g0072 a0001c0006t0004g0179 |
3 | HG03225.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1088+565C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722154 | |||||||
chr3:179722235 | C | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(85): Show |
88 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.1088+646C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722235 | |||||||
chr3:179722303 | T | A | 3 | a0001c0002t0001g0134 a0001c0004t0034g0072 a0001c0006t0004g0179 |
3 | HG03225.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1088+714T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722303 | |||||||
chr3:179722319 | G | C | 81 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1088+730G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722319 | |||||||
chr3:179722398 | A | G | 35 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0066 others(32): Show |
35 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1088+809A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722398 | |||||||
chr3:179722406 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(95): Show |
98 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.1088+817G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722406 | |||||||
chr3:179722432 | T | C | 3 | a0001c0002t0004g0143 a0001c0002t0016g0173 a0001c0002t0033g0174 |
3 | HG02630.hp2 HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1088+843T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722432 | |||||||
chr3:179722596 | G | A | 3 | a0001c0002t0001g0134 a0001c0004t0034g0072 a0001c0006t0004g0179 |
3 | HG03225.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1088+1007G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722596 | |||||||
chr3:179722613 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1088+1024A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722613 | |||||||
chr3:179722647 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1088+1058C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722647 | |||||||
chr3:179722791 | C | T | 187 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(184): Show |
187 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1088+1202C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722791 | |||||||
chr3:179722795 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1088+1206A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722795 | |||||||
chr3:179722836 | C | T | 5 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0001t0008g0293 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+1247C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179722836 | |||||||
chr3:179723026 | G | A | 2 | a0001c0006t0006g0181 a0001c0006t0032g0140 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1088+1437G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723026 | |||||||
chr3:179723042 | T | C | 3 | a0001c0002t0001g0134 a0001c0004t0034g0072 a0001c0006t0004g0179 |
3 | HG03225.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1088+1453T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723042 | |||||||
chr3:179723054 | G | A | 2 | a0001c0001t0022g0257 a0001c0002t0001g0139 |
2 | HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1088+1465G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723054 | |||||||
chr3:179723066 | C | T | 2 | a0001c0006t0006g0181 a0001c0006t0032g0140 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1088+1477C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723066 | |||||||
chr3:179723290 | T | C | 246 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(243): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1088+1701T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723290 | |||||||
chr3:179723380 | A | G | 8 | a0001c0001t0005g0202 a0001c0001t0005g0231 a0001c0001t0005g0232 others(5): Show |
8 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1088+1791A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723380 | |||||||
chr3:179723633 | T | C | 85 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1088+2044T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723633 | |||||||
chr3:179723648 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1088+2059C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723648 | |||||||
chr3:179723713 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1088+2124A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723713 | |||||||
chr3:179723726 | T | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0108 a0001c0001t0001g0278 others(4): Show |
7 | HG01952.hp1 NA18612.hp2 NA19055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1088+2137T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723726 | |||||||
chr3:179723729 | C | G | 3 | a0001c0008t0008g0237 a0001c0008t0008g0265 a0001c0015t0008g0133 |
3 | HG01109.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1088+2140C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723729 | |||||||
chr3:179723785 | C | G | 2 | a0001c0001t0002g0120 a0001c0002t0002g0147 |
2 | NA18943.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1088+2196C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723785 | |||||||
chr3:179723790 | C | A | 1 | a0001c0002t0041g0124 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1088+2201C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723790 | |||||||
chr3:179723994 | AT | A | 3 | a0001c0001t0001g0222 a0001c0001t0036g0285 a0001c0002t0002g0127 |
3 | HG01257.hp2 NA18941.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1088+2408delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179723994 | ||||||
chr3:179723997 | T | A | 39 | a0001c0001t0001g0211 a0001c0001t0001g0279 a0001c0001t0002g0005 others(36): Show |
40 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1088+2408T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723997 | |||||||
chr3:179723998 | A | T | 5 | a0001c0001t0006g0297 a0001c0001t0022g0257 a0001c0002t0001g0139 others(2): Show |
5 | HG01109.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088+2409A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179723998 | |||||||
chr3:179724073 | T | C | 3 | a0001c0008t0008g0237 a0001c0008t0008g0265 a0001c0015t0008g0133 |
3 | HG01109.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1088+2484T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724073 | |||||||
chr3:179724147 | A | G | 1 | a0001c0001t0028g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1088+2558A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724147 | |||||||
chr3:179724179 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA18999.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1088+2590C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724179 | |||||||
chr3:179724315 | G | A | 5 | a0001c0001t0006g0297 a0001c0001t0022g0257 a0001c0002t0001g0139 others(2): Show |
5 | HG01109.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088+2726G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724315 | |||||||
chr3:179724350 | C | T | 81 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1088+2761C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724350 | |||||||
chr3:179724407 | G | A | 1 | a0001c0002t0041g0124 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1088+2818G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724407 | |||||||
chr3:179724441 | A | G | 192 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(189): Show |
192 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1088+2852A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724441 | |||||||
chr3:179724460 | G | GA | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(85): Show |
88 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.1088+2887dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179724460 | ||||||
chr3:179724460 | G | GAA | 20 | a0001c0001t0002g0272 a0001c0001t0004g0206 a0001c0001t0008g0040 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1088+2886_1088+288 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179724460 | ||||||
chr3:179724491 | T | G | 81 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1088+2902T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724491 | |||||||
chr3:179724542 | A | G | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1088+2953A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724542 | |||||||
chr3:179724955 | C | T | 5 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0001t0008g0293 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+3366C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179724955 | |||||||
chr3:179725059 | A | C | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1088+3470A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725059 | |||||||
chr3:179725073 | G | A | 1 | a0001c0001t0010g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1088+3484G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725073 | |||||||
chr3:179725291 | C | T | 1 | a0001c0009t0005g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1088+3702C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725291 | |||||||
chr3:179725298 | G | GT | 10 | a0001c0001t0018g0191 a0001c0003t0001g0255 a0001c0003t0001g0290 others(7): Show |
10 | HG01255.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1088+3718dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179725298 | ||||||
chr3:179725301 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1088+3712T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725301 | |||||||
chr3:179725397 | A | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1088+3808A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725397 | |||||||
chr3:179725578 | A | G | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1088+3989A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725578 | |||||||
chr3:179725643 | T | C | 247 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(244): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1088+4054T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725643 | |||||||
chr3:179725713 | T | C | 6 | a0001c0001t0018g0191 a0001c0003t0001g0290 a0001c0005t0001g0142 others(3): Show |
6 | HG01255.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088+4124T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725713 | |||||||
chr3:179725752 | G | T | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1088+4163G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725752 | |||||||
chr3:179725805 | G | A | 5 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0001t0008g0293 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+4216G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179725805 | |||||||
chr3:179726005 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1089-4184G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179726005 | |||||||
chr3:179726122 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1089-4067C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179726122 | |||||||
chr3:179726248 | G | A | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-3941G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179726248 | |||||||
chr3:179726427 | A | G | 294 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(291): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1089-3762A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179726427 | |||||||
chr3:179726662 | A | G | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-3527A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179726662 | |||||||
chr3:179726682 | CT | C | 245 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(242): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1089-3494delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179726682 | ||||||
chr3:179726782 | A | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(45): Show |
48 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1089-3407A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179726782 | |||||||
chr3:179727030 | TAAC | T | 12 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(9): Show |
12 | HG00140.hp2 HG01099.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1089-3153_1089-315 others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727030 | ||||||
chr3:179727060 | A | G | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-3129A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727060 | |||||||
chr3:179727163 | G | GT | 49 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0211 others(46): Show |
49 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1089-3005dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727163 | ||||||
chr3:179727163 | GT | G | 12 | a0001c0001t0001g0050 a0001c0001t0001g0220 a0001c0001t0004g0234 others(9): Show |
12 | HG01081.hp2 HG02055.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1089-3005delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727163 | ||||||
chr3:179727163 | GTT | G | 52 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(49): Show |
52 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1089-3006_1089-300 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727163 | ||||||
chr3:179727163 | GTTT | G | 50 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0064 others(47): Show |
50 | HG01109.hp2 HG01255.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.1089-3007_1089-300 others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727163 | ||||||
chr3:179727184 | T | A | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-3005T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727184 | |||||||
chr3:179727280 | A | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(176): Show |
179 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1089-2909A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727280 | |||||||
chr3:179727282 | T | A | 1 | a0002c0007t0001g0243 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1089-2907T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727282 | |||||||
chr3:179727319 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0287 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1089-2870T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727319 | |||||||
chr3:179727343 | T | A | 82 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(79): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1089-2846T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727343 | |||||||
chr3:179727366 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1089-2823C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727366 | |||||||
chr3:179727435 | T | C | 247 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(244): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1089-2754T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727435 | |||||||
chr3:179727449 | C | T | 246 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(243): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1089-2740C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727449 | |||||||
chr3:179727467 | T | G | 1 | a0001c0001t0036g0285 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1089-2722T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727467 | |||||||
chr3:179727616 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(46): Show |
49 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1089-2573C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727616 | |||||||
chr3:179727623 | C | G | 1 | a0001c0001t0003g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1089-2566C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727623 | |||||||
chr3:179727655 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1089-2534A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727655 | |||||||
chr3:179727682 | T | C | 1 | a0001c0001t0003g0244 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1089-2507T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727682 | |||||||
chr3:179727695 | C | T | 11 | a0001c0001t0018g0191 a0001c0001t0030g0258 a0001c0003t0001g0255 others(8): Show |
11 | HG01255.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1089-2494C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727695 | |||||||
chr3:179727703 | T | TG | 193 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(190): Show |
193 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1089-2485dupG | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727703 | ||||||
chr3:179727703 | T | TGGCCAGG others(121): Show |
1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1089-2485_1089-248 others(132): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727703 | ||||||
chr3:179727707 | A | G | 13 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(10): Show |
13 | HG00140.hp2 HG01099.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1089-2482A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727707 | |||||||
chr3:179727707 | AGGCAGAG others(123): Show |
A | 3 | a0001c0001t0015g0292 a0001c0002t0015g0130 a0001c0003t0001g0239 |
3 | HG02055.hp2 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1089-2405_1089-227 others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727707 | ||||||
chr3:179727728 | C | T | 82 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(79): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1089-2461C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727728 | |||||||
chr3:179727753 | C | T | 4 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0002t0008g0164 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-2436C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727753 | |||||||
chr3:179727768 | G | A | 4 | a0001c0001t0005g0231 a0001c0001t0005g0233 a0001c0002t0004g0172 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-2421G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727768 | |||||||
chr3:179727789 | A | G | 1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1089-2400A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727789 | |||||||
chr3:179727798 | AC | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(95): Show |
98 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.1089-2381delC | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727798 | ||||||
chr3:179727798 | ACC | A | 135 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(132): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1089-2382_1089-238 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727798 | ||||||
chr3:179727799 | C | CCCCCCCC others(43): Show |
1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1089-2382_1089-238 others(54): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727799 | ||||||
chr3:179727800 | C | CCCCCCAC others(118): Show |
1 | a0001c0001t0008g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1089-2384_1089-238 others(129): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727800 | ||||||
chr3:179727801 | C | CCCCCACC others(117): Show |
1 | a0001c0001t0004g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1089-2384_1089-238 others(128): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727801 | ||||||
chr3:179727801 | C | CCCCCACC others(117): Show |
2 | a0001c0002t0008g0164 a0001c0002t0008g0165 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1089-2384_1089-238 others(128): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727801 | ||||||
chr3:179727803 | C | T | 12 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(9): Show |
12 | HG00140.hp2 HG01099.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1089-2386C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727803 | |||||||
chr3:179727805 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0026g0049 a0001c0002t0001g0145 |
3 | NA18966.hp1 NA18995.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1089-2384C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727805 | |||||||
chr3:179727808 | C | G | 2 | a0001c0001t0001g0203 a0001c0002t0001g0134 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1089-2381C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727808 | |||||||
chr3:179727821 | G | A | 5 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0001t0008g0293 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-2368G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727821 | |||||||
chr3:179727822 | A | G | 5 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0001t0008g0293 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-2367A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727822 | |||||||
chr3:179727828 | C | CGGCTGGC others(121): Show |
1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-2320_1089-231 others(132): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727828 | ||||||
chr3:179727828 | C | CGGCTGGC others(120): Show |
9 | a0001c0001t0018g0191 a0001c0003t0001g0255 a0001c0003t0001g0290 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1089-2275_1089-227 others(131): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727828 | ||||||
chr3:179727828 | C | CGGCTGGC others(120): Show |
3 | a0001c0001t0001g0277 a0001c0001t0001g0287 a0001c0002t0001g0131 |
3 | HG02258.hp2 HG03098.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1089-2275_1089-227 others(131): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727828 | ||||||
chr3:179727828 | C | CGGCTGGC others(375): Show |
43 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(40): Show |
44 | HG00140.hp1 HG00673.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1089-2275_1089-227 others(386): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727828 | ||||||
chr3:179727828 | C | CGGCTGGC others(630): Show |
1 | a0001c0001t0002g0216 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1089-2275_1089-227 others(641): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727828 | ||||||
chr3:179727828 | C | CGGCTGGC others(376): Show |
1 | a0001c0001t0002g0119 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1089-2275_1089-227 others(387): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727828 | ||||||
chr3:179727828 | C | CGGCTGGC others(120): Show |
8 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(5): Show |
8 | HG00140.hp2 HG01099.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089-2321_1089-232 others(131): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727828 | ||||||
chr3:179727828 | C | CGGCTGGC others(297): Show |
3 | a0001c0002t0004g0172 a0001c0002t0004g0187 a0001c0002t0004g0270 |
3 | HG02280.hp1 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1089-2349_1089-234 others(308): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727828 | ||||||
chr3:179727828 | C | T | 5 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0001t0008g0293 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-2361C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727828 | |||||||
chr3:179727829 | GGCTGGCC others(268): Show |
G | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1089-2274_1089-200 others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727829 | ||||||
chr3:179727836 | C | CGGGCAGA others(120): Show |
2 | a0001c0001t0014g0184 a0001c0001t0014g0276 |
2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1089-2275_1089-227 others(131): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727836 | ||||||
chr3:179727869 | C | T | 4 | a0001c0004t0002g0182 a0001c0004t0002g0267 a0001c0006t0001g0153 others(1): Show |
4 | HG02683.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-2320C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727869 | |||||||
chr3:179727891 | ACCTCCCG others(141): Show |
A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(114): Show |
117 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1089-2274_1089-212 others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727891 | ||||||
chr3:179727911 | GGCCAGGT others(140): Show |
G | 1 | a0001c0001t0002g0272 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1089-2276_1089-213 others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727911 | ||||||
chr3:179727915 | A | G | 48 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.1089-2274A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727915 | |||||||
chr3:179727918 | T | C | 48 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.1089-2271T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727918 | |||||||
chr3:179727929 | C | A | 4 | a0001c0004t0002g0182 a0001c0004t0002g0267 a0001c0006t0001g0153 others(1): Show |
4 | HG02683.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-2260C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727929 | |||||||
chr3:179727940 | C | CCCTCCCG others(71): Show |
6 | a0001c0001t0002g0045 a0001c0002t0002g0149 a0001c0004t0002g0182 others(3): Show |
6 | HG02683.hp2 HG02735.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1089-2245_1089-224 others(82): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727940 | ||||||
chr3:179727940 | C | CCCTCCCG others(71): Show |
39 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(36): Show |
39 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.1089-2245_1089-224 others(82): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727940 | ||||||
chr3:179727945 | T | C | 56 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(53): Show |
56 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1089-2244T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727945 | |||||||
chr3:179727947 | G | A | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2242G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727947 | |||||||
chr3:179727948 | G | A | 3 | a0001c0004t0034g0072 a0001c0005t0001g0150 a0001c0006t0004g0179 |
3 | HG03225.hp2 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2241G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727948 | |||||||
chr3:179727949 | A | G | 3 | a0001c0004t0034g0072 a0001c0005t0001g0150 a0001c0006t0004g0179 |
3 | HG03225.hp2 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2240A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727949 | |||||||
chr3:179727951 | G | A | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2238G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727951 | |||||||
chr3:179727952 | A | G | 56 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(53): Show |
56 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1089-2237A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727952 | |||||||
chr3:179727955 | C | T | 3 | a0001c0004t0034g0072 a0001c0005t0001g0150 a0001c0006t0004g0179 |
3 | HG03225.hp2 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2234C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727955 | |||||||
chr3:179727963 | T | C | 46 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(43): Show |
46 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.1089-2226T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727963 | |||||||
chr3:179727964 | G | A | 45 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(42): Show |
45 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.1089-2225G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727964 | |||||||
chr3:179727967 | C | T | 45 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(42): Show |
45 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.1089-2222C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727967 | |||||||
chr3:179727968 | G | A | 2 | a0001c0004t0034g0072 a0001c0006t0004g0179 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2221G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727968 | |||||||
chr3:179727969 | G | A | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2220G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727969 | |||||||
chr3:179727970 | G | A | 2 | a0001c0004t0034g0072 a0001c0006t0004g0179 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2219G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727970 | |||||||
chr3:179727976 | G | C | 2 | a0001c0004t0034g0072 a0001c0006t0004g0179 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2213G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727976 | |||||||
chr3:179727979 | C | T | 2 | a0001c0004t0034g0072 a0001c0006t0004g0179 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2210C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727979 | |||||||
chr3:179727980 | C | T | 2 | a0001c0004t0034g0072 a0001c0006t0004g0179 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2209C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727980 | |||||||
chr3:179727982 | CCCACCTC others(43): Show |
C | 5 | a0001c0001t0001g0260 a0001c0001t0003g0026 a0001c0001t0004g0261 others(2): Show |
5 | HG01934.hp1 HG02486.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-2193_1089-214 others(54): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179727982 | ||||||
chr3:179727983 | C | CAGTAGGG others(17): Show |
2 | a0001c0004t0034g0072 a0001c0006t0004g0179 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2206_1089-220 others(28): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727983 | |||||||
chr3:179727983 | C | T | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2206C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727983 | |||||||
chr3:179727985 | A | C | 2 | a0001c0004t0034g0072 a0001c0006t0004g0179 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1089-2204A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727985 | |||||||
chr3:179727991 | C | T | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2198C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727991 | |||||||
chr3:179727994 | C | T | 41 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(38): Show |
41 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.1089-2195C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727994 | |||||||
chr3:179727996 | A | G | 70 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(67): Show |
70 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.1089-2193A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727996 | |||||||
chr3:179727998 | A | T | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2191A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727998 | |||||||
chr3:179727999 | C | A | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2190C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179727999 | |||||||
chr3:179728001 | G | A | 41 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(38): Show |
41 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.1089-2188G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728001 | |||||||
chr3:179728008 | T | C | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2181T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728008 | |||||||
chr3:179728011 | C | G | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2178C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728011 | |||||||
chr3:179728012 | C | T | 45 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(42): Show |
45 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.1089-2177C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728012 | |||||||
chr3:179728013 | A | G | 45 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(42): Show |
45 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.1089-2176A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728013 | |||||||
chr3:179728015 | G | A | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2174G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728015 | |||||||
chr3:179728016 | T | C | 45 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(42): Show |
45 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.1089-2173T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728016 | |||||||
chr3:179728016 | T | G | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2173T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728016 | |||||||
chr3:179728018 | G | C | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2171G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728018 | |||||||
chr3:179728026 | AT | A | 47 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(44): Show |
47 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.1089-2162delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728026 | |||||||
chr3:179728032 | A | ACCACCTC others(42): Show |
1 | a0001c0001t0004g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1089-2127_1089-212 others(53): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179728032 | ||||||
chr3:179728032 | A | ACCACCTC others(140): Show |
2 | a0001c0001t0014g0184 a0001c0001t0014g0276 |
2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1089-2097_1089-209 others(151): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179728032 | ||||||
chr3:179728032 | A | C | 47 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(44): Show |
47 | HG01109.hp1 HG01109.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.1089-2157A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728032 | |||||||
chr3:179728032 | A | G | 8 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(5): Show |
8 | HG00140.hp2 HG01099.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089-2157A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728032 | |||||||
chr3:179728032 | A | T | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2157A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728032 | |||||||
chr3:179728039 | C | A | 1 | a0001c0005t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-2150C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728039 | |||||||
chr3:179728046 | G | A | 2 | a0001c0001t0002g0045 a0001c0002t0002g0149 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1089-2143G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728046 | |||||||
chr3:179728048 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1089-2141A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728048 | |||||||
chr3:179728054 | C | T | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1089-2135C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728054 | |||||||
chr3:179728055 | GGCTGGCC others(42): Show |
G | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1089-2122_1089-207 others(53): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179728055 | ||||||
chr3:179728063 | G | A | 5 | a0001c0001t0004g0236 a0001c0004t0002g0182 a0001c0004t0002g0267 others(2): Show |
5 | HG02683.hp2 HG03041.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-2126G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728063 | |||||||
chr3:179728066 | C | T | 5 | a0001c0001t0004g0236 a0001c0004t0002g0182 a0001c0004t0002g0267 others(2): Show |
5 | HG02683.hp2 HG03041.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-2123C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728066 | |||||||
chr3:179728073 | C | T | 2 | a0001c0006t0006g0181 a0001c0006t0032g0140 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1089-2116C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728073 | |||||||
chr3:179728076 | A | AT | 4 | a0001c0004t0002g0182 a0001c0004t0002g0267 a0001c0006t0001g0153 others(1): Show |
4 | HG02683.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-2113_1089-211 others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728076 | |||||||
chr3:179728077 | C | A | 70 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(67): Show |
70 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1089-2112C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728077 | |||||||
chr3:179728081 | C | G | 4 | a0001c0004t0002g0182 a0001c0004t0002g0267 a0001c0006t0001g0153 others(1): Show |
4 | HG02683.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-2108C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728081 | |||||||
chr3:179728096 | G | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(115): Show |
118 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1089-2093G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728096 | |||||||
chr3:179728097 | A | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(115): Show |
118 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1089-2092A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728097 | |||||||
chr3:179728098 | C | T | 1 | a0001c0001t0002g0114 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1089-2091C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728098 | |||||||
chr3:179728103 | C | T | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(115): Show |
118 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1089-2086C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728103 | |||||||
chr3:179728104 | A | G | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(118): Show |
121 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1089-2085A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728104 | |||||||
chr3:179728110 | C | G | 1 | a0001c0006t0004g0179 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1089-2079C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728110 | |||||||
chr3:179728111 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(45): Show |
48 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1089-2078C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728111 | |||||||
chr3:179728140 | G | C | 3 | a0001c0001t0001g0039 a0001c0001t0026g0049 a0001c0002t0001g0145 |
3 | NA18966.hp1 NA18995.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1089-2049G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728140 | |||||||
chr3:179728172 | C | T | 1 | a0001c0002t0001g0131 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1089-2017C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728172 | |||||||
chr3:179728222 | A | G | 189 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(186): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1089-1967A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728222 | |||||||
chr3:179728270 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1089-1919C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728270 | |||||||
chr3:179728271 | A | G | 82 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(79): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1089-1918A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728271 | |||||||
chr3:179728305 | C | T | 9 | a0001c0001t0006g0297 a0001c0001t0022g0257 a0001c0002t0001g0139 others(6): Show |
9 | HG01109.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1089-1884C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728305 | |||||||
chr3:179728324 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1089-1865C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728324 | |||||||
chr3:179728336 | C | G | 1 | a0001c0001t0005g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1089-1853C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728336 | |||||||
chr3:179728338 | C | T | 1 | a0001c0002t0004g0187 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1089-1851C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728338 | |||||||
chr3:179728339 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(93): Show |
96 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.1089-1850G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728339 | |||||||
chr3:179728344 | G | A | 2 | a0001c0001t0003g0022 a0001c0001t0003g0042 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1089-1845G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728344 | |||||||
chr3:179728466 | C | T | 10 | a0001c0001t0018g0191 a0001c0003t0001g0255 a0001c0003t0001g0290 others(7): Show |
10 | HG01255.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1089-1723C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728466 | |||||||
chr3:179728479 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1089-1710A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728479 | |||||||
chr3:179728482 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1089-1707C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728482 | |||||||
chr3:179728535 | C | T | 2 | a0001c0001t0001g0096 a0001c0002t0001g0167 |
2 | HG00738.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1089-1654C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728535 | |||||||
chr3:179728557 | A | G | 22 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(19): Show |
22 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1089-1632A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728557 | |||||||
chr3:179728574 | C | CG | 7 | a0001c0001t0001g0212 a0001c0001t0002g0272 a0001c0001t0006g0273 others(4): Show |
7 | HG00621.hp2 HG00741.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1089-1611dupG | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179728574 | ||||||
chr3:179728577 | G | A | 1 | a0001c0001t0002g0216 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1089-1612G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728577 | |||||||
chr3:179728586 | C | T | 2 | a0001c0001t0001g0080 a0001c0003t0001g0255 |
2 | HG02559.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1089-1603C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728586 | |||||||
chr3:179728606 | A | G | 172 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(169): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1089-1583A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728606 | |||||||
chr3:179728659 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0225 |
3 | HG01993.hp1 HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1089-1530G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728659 | |||||||
chr3:179728667 | G | A | 9 | a0001c0001t0018g0191 a0001c0003t0001g0290 a0001c0005t0001g0142 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1089-1522G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728667 | |||||||
chr3:179728699 | A | C | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-1490A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728699 | |||||||
chr3:179728702 | G | C | 1 | a0001c0003t0001g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1089-1487G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728702 | |||||||
chr3:179728716 | C | A | 82 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(79): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1089-1473C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728716 | |||||||
chr3:179728718 | G | C | 1 | a0001c0001t0002g0037 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1089-1471G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728718 | |||||||
chr3:179728788 | G | C | 82 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(79): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1089-1401G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728788 | |||||||
chr3:179728859 | A | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(221): Show |
224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1089-1330A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179728859 | |||||||
chr3:179728906 | T | TACCC | 86 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(83): Show |
86 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.1089-1280_1089-127 others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179728906 | ||||||
chr3:179728930 | C | CAGAGGGA others(16): Show |
12 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(9): Show |
12 | HG00140.hp2 HG01099.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1089-1243_1089-122 others(27): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179728930 | ||||||
chr3:179728930 | CAGAGGGA others(16): Show |
C | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-1243_1089-122 others(27): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179728930 | ||||||
chr3:179728982 | A | AAGAGGG | 180 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(177): Show |
180 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.1089-1190_1089-118 others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179728982 | ||||||
chr3:179729360 | A | G | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1089-829A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179729360 | |||||||
chr3:179729387 | C | T | 3 | a0001c0001t0006g0297 a0001c0002t0004g0170 a0001c0002t0006g0169 |
3 | HG01109.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1089-802C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179729387 | |||||||
chr3:179729390 | G | A | 70 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(67): Show |
70 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1089-799G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179729390 | |||||||
chr3:179729511 | A | G | 1 | a0001c0001t0011g0065 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1089-678A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179729511 | |||||||
chr3:179729619 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1089-570G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179729619 | |||||||
chr3:179729632 | T | C | 71 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(68): Show |
71 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1089-557T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179729632 | |||||||
chr3:179729634 | G | A | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-555G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179729634 | |||||||
chr3:179729706 | C | A | 193 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(190): Show |
193 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1089-483C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179729706 | |||||||
chr3:179729712 | T | G | 2 | a0003c0010t0009g0069 a0003c0010t0009g0102 |
2 | HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1089-477T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179729712 | |||||||
chr3:179730024 | G | A | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1089-165G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179730024 | |||||||
chr3:179730064 | T | A | 52 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(49): Show |
53 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1089-125T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179730064 | |||||||
chr3:179730097 | G | T | 9 | a0001c0003t0001g0255 a0001c0003t0001g0290 a0001c0005t0001g0142 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1089-92G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179730097 | |||||||
chr3:179730126 | G | T | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1089-63G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | chr3 | 179730126 | |||||||
chr3:179730141 | GTTC | G | 9 | a0001c0003t0001g0255 a0001c0003t0001g0290 a0001c0005t0001g0142 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1089-42_1089-40del others(3): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 179730141 | ||||||
chr3:179730278 | AT | A | 272 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(269): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1160+29delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr3 | 179730278 | ||||||
chr3:179730595 | C | T | 193 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(190): Show |
193 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1161-21C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 9/20 | chr3 | 179730595 | |||||||
chr3:179731081 | C | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(176): Show |
179 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1254+372C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731081 | |||||||
chr3:179731176 | C | T | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1254+467C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731176 | |||||||
chr3:179731200 | T | C | 72 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(69): Show |
72 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1254+491T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731200 | |||||||
chr3:179731208 | C | A | 1 | a0001c0001t0004g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1254+499C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731208 | |||||||
chr3:179731629 | T | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+920T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731629 | |||||||
chr3:179731729 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(9): Show |
12 | HG00558.hp1 HG01934.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1254+1020C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731729 | |||||||
chr3:179731748 | G | A | 1 | a0001c0001t0009g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1254+1039G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731748 | |||||||
chr3:179731800 | C | T | 1 | a0001c0001t0005g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1254+1091C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731800 | |||||||
chr3:179731830 | T | A | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1254+1121T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731830 | |||||||
chr3:179731831 | C | A | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1254+1122C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731831 | |||||||
chr3:179731852 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1254+1143G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179731852 | |||||||
chr3:179731989 | C | CAAGAGAA others(13): Show |
5 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0001t0008g0293 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+1295_1254+129 others(24): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr3 | 179731989 | ||||||
chr3:179732005 | G | A | 245 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(242): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1254+1296G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732005 | |||||||
chr3:179732110 | A | G | 14 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0001t0008g0293 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1254+1401A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732110 | |||||||
chr3:179732202 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0017g0192 a0001c0002t0001g0185 |
3 | HG02486.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1254+1493G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732202 | |||||||
chr3:179732320 | A | G | 1 | a0001c0001t0005g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1254+1611A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732320 | |||||||
chr3:179732418 | G | T | 1 | a0001c0002t0001g0131 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1254+1709G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732418 | |||||||
chr3:179732501 | A | G | 5 | a0001c0001t0001g0082 a0001c0001t0001g0278 a0001c0001t0001g0281 others(2): Show |
5 | HG01952.hp1 NA19055.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+1792A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732501 | |||||||
chr3:179732540 | T | G | 1 | a0001c0001t0012g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1254+1831T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732540 | |||||||
chr3:179732635 | T | G | 5 | a0001c0001t0004g0206 a0001c0001t0008g0040 a0001c0001t0008g0293 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+1926T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732635 | |||||||
chr3:179732738 | T | C | 1 | a0001c0001t0004g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1254+2029T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732738 | |||||||
chr3:179732745 | T | TA | 72 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(69): Show |
72 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1254+2043dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr3 | 179732745 | ||||||
chr3:179732747 | A | C | 46 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(43): Show |
46 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.1254+2038A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732747 | |||||||
chr3:179732775 | A | G | 1 | a0001c0001t0002g0256 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1254+2066A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732775 | |||||||
chr3:179732849 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1254+2140G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732849 | |||||||
chr3:179732860 | G | A | 52 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(49): Show |
53 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1254+2151G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179732860 | |||||||
chr3:179733034 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1254+2325G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179733034 | |||||||
chr3:179733055 | G | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(46): Show |
49 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1254+2346G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179733055 | |||||||
chr3:179733482 | C | G | 167 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0043 others(164): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1254+2773C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179733482 | |||||||
chr3:179733584 | C | T | 7 | a0001c0001t0006g0297 a0001c0001t0022g0257 a0001c0002t0001g0139 others(4): Show |
7 | HG01109.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+2875C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179733584 | |||||||
chr3:179733678 | G | A | 53 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(50): Show |
54 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1254+2969G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179733678 | |||||||
chr3:179733722 | T | C | 1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1254+3013T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179733722 | |||||||
chr3:179733813 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1254+3104A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179733813 | |||||||
chr3:179734045 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1254+3336A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179734045 | |||||||
chr3:179734099 | C | A | 52 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(49): Show |
53 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1254+3390C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179734099 | |||||||
chr3:179734162 | C | CT | 5 | a0001c0001t0006g0297 a0001c0001t0022g0257 a0001c0002t0001g0139 others(2): Show |
5 | HG01109.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+3458dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr3 | 179734162 | ||||||
chr3:179734193 | T | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+3484T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179734193 | |||||||
chr3:179734285 | G | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+3576G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179734285 | |||||||
chr3:179734326 | A | G | 1 | a0001c0002t0004g0143 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1254+3617A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179734326 | |||||||
chr3:179734728 | A | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+4019A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179734728 | |||||||
chr3:179734883 | C | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+4174C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179734883 | |||||||
chr3:179734918 | C | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+4209C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179734918 | |||||||
chr3:179734988 | T | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+4279T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179734988 | |||||||
chr3:179735100 | A | G | 245 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(242): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1254+4391A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735100 | |||||||
chr3:179735104 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0093 a0001c0001t0001g0100 others(1): Show |
4 | HG01891.hp2 HG02602.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+4395C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735104 | |||||||
chr3:179735234 | C | T | 2 | a0001c0001t0004g0105 a0001c0001t0004g0236 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1254+4525C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735234 | |||||||
chr3:179735235 | G | A | 1 | a0001c0001t0002g0216 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1254+4526G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735235 | |||||||
chr3:179735284 | C | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+4575C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735284 | |||||||
chr3:179735416 | C | CT | 24 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(21): Show |
24 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1254+4720dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr3 | 179735416 | ||||||
chr3:179735416 | CT | C | 54 | a0001c0001t0001g0051 a0001c0001t0001g0211 a0001c0001t0001g0222 others(51): Show |
55 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1254+4720delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr3 | 179735416 | ||||||
chr3:179735439 | A | G | 2 | a0001c0004t0034g0072 a0001c0006t0032g0140 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1254+4730A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735439 | |||||||
chr3:179735643 | A | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-4604A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735643 | |||||||
chr3:179735659 | C | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-4588C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735659 | |||||||
chr3:179735741 | T | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-4506T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735741 | |||||||
chr3:179735772 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1255-4475C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735772 | |||||||
chr3:179735773 | G | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-4474G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735773 | |||||||
chr3:179735851 | A | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1255-4396A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735851 | |||||||
chr3:179735941 | G | A | 2 | a0001c0001t0012g0070 a0001c0001t0012g0113 |
2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1255-4306G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735941 | |||||||
chr3:179735975 | G | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-4272G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735975 | |||||||
chr3:179735998 | C | T | 1 | a0001c0001t0011g0065 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1255-4249C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179735998 | |||||||
chr3:179736090 | A | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-4157A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736090 | |||||||
chr3:179736207 | T | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-4040T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736207 | |||||||
chr3:179736233 | A | G | 1 | a0001c0002t0003g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1255-4014A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736233 | |||||||
chr3:179736294 | G | A | 1 | a0001c0004t0012g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1255-3953G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736294 | |||||||
chr3:179736379 | G | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-3868G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736379 | |||||||
chr3:179736445 | A | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-3802A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736445 | |||||||
chr3:179736496 | A | T | 1 | a0001c0003t0039g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1255-3751A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736496 | |||||||
chr3:179736606 | A | G | 4 | a0001c0008t0004g0264 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-3641A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736606 | |||||||
chr3:179736638 | A | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-3609A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736638 | |||||||
chr3:179736665 | C | T | 1 | a0001c0001t0011g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1255-3582C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736665 | |||||||
chr3:179736941 | G | A | 4 | a0001c0008t0004g0264 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-3306G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179736941 | |||||||
chr3:179737120 | G | GTGTT | 10 | a0001c0003t0001g0230 a0001c0003t0001g0255 a0001c0003t0001g0290 others(7): Show |
10 | HG01255.hp2 HG01433.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1255-3126_1255-312 others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr3 | 179737120 | ||||||
chr3:179737203 | A | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-3044A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737203 | |||||||
chr3:179737203 | AT | A | 5 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0071 others(2): Show |
5 | HG00621.hp1 HG02080.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255-3043delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737203 | |||||||
chr3:179737337 | A | C | 71 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(68): Show |
71 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1255-2910A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737337 | |||||||
chr3:179737461 | T | C | 1 | a0001c0001t0003g0294 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1255-2786T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737461 | |||||||
chr3:179737493 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1255-2754C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737493 | |||||||
chr3:179737494 | G | A | 10 | a0001c0003t0001g0230 a0001c0003t0001g0255 a0001c0003t0001g0290 others(7): Show |
10 | HG01255.hp2 HG01433.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1255-2753G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737494 | |||||||
chr3:179737525 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0017g0192 a0001c0002t0001g0185 |
3 | HG02486.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1255-2722C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737525 | |||||||
chr3:179737553 | T | A | 3 | a0001c0001t0001g0260 a0001c0001t0017g0192 a0001c0002t0001g0185 |
3 | HG02486.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1255-2694T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737553 | |||||||
chr3:179737652 | G | A | 53 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(50): Show |
54 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1255-2595G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737652 | |||||||
chr3:179737823 | C | T | 188 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(185): Show |
189 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1255-2424C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179737823 | |||||||
chr3:179738008 | G | A | 5 | a0001c0001t0006g0035 a0001c0001t0007g0099 a0001c0001t0007g0106 others(2): Show |
5 | HG00323.hp2 HG00738.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255-2239G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738008 | |||||||
chr3:179738077 | C | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-2170C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738077 | |||||||
chr3:179738141 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1255-2106C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738141 | |||||||
chr3:179738169 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0093 a0001c0001t0001g0100 others(1): Show |
4 | HG01891.hp2 HG02602.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-2078C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738169 | |||||||
chr3:179738222 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1255-2025A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738222 | |||||||
chr3:179738315 | T | G | 4 | a0001c0001t0007g0268 a0001c0002t0007g0001 a0001c0002t0007g0168 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255-1932T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738315 | |||||||
chr3:179738365 | T | C | 1 | a0001c0002t0009g0141 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1255-1882T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738365 | |||||||
chr3:179738478 | A | G | 1 | a0003c0010t0009g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1255-1769A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738478 | |||||||
chr3:179738509 | C | T | 1 | a0001c0001t0004g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1255-1738C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738509 | |||||||
chr3:179738744 | G | A | 139 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(136): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1255-1503G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738744 | |||||||
chr3:179738798 | A | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(46): Show |
49 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1255-1449A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738798 | |||||||
chr3:179738863 | C | T | 1 | a0001c0001t0005g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1255-1384C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738863 | |||||||
chr3:179738948 | G | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-1299G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179738948 | |||||||
chr3:179739100 | A | G | 71 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(68): Show |
71 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1255-1147A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739100 | |||||||
chr3:179739135 | G | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-1112G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739135 | |||||||
chr3:179739146 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1255-1101C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739146 | |||||||
chr3:179739151 | T | A | 52 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(49): Show |
53 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1255-1096T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739151 | |||||||
chr3:179739235 | G | C | 3 | a0001c0001t0001g0260 a0001c0001t0017g0192 a0001c0002t0001g0185 |
3 | HG02486.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1255-1012G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739235 | |||||||
chr3:179739252 | C | G | 2 | a0001c0001t0017g0192 a0001c0001t0030g0258 |
2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1255-995C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739252 | |||||||
chr3:179739314 | T | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-933T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739314 | |||||||
chr3:179739488 | G | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-759G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739488 | |||||||
chr3:179739587 | T | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-660T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739587 | |||||||
chr3:179739596 | C | T | 71 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(68): Show |
71 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1255-651C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739596 | |||||||
chr3:179739619 | G | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-628G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739619 | |||||||
chr3:179739626 | C | T | 4 | a0001c0008t0004g0264 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-621C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739626 | |||||||
chr3:179739931 | C | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-316C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739931 | |||||||
chr3:179739954 | G | A | 6 | a0001c0001t0008g0198 a0001c0001t0015g0292 a0001c0001t0024g0235 others(3): Show |
6 | HG00735.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-293G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739954 | |||||||
chr3:179739964 | T | C | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1255-283T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179739964 | |||||||
chr3:179740002 | C | T | 51 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(48): Show |
52 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1255-245C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179740002 | |||||||
chr3:179740057 | G | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255-190G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179740057 | |||||||
chr3:179740157 | G | A | 1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1255-90G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 10/20 | chr3 | 179740157 | |||||||
chr3:179740384 | G | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1380+12G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740384 | |||||||
chr3:179740421 | C | T | 1 | a0001c0003t0039g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1380+49C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740421 | |||||||
chr3:179740440 | T | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1380+68T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740440 | |||||||
chr3:179740454 | C | G | 1 | a0001c0001t0023g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1380+82C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740454 | |||||||
chr3:179740525 | T | G | 6 | a0001c0001t0001g0222 a0001c0001t0002g0024 a0001c0001t0002g0089 others(3): Show |
6 | HG01257.hp2 NA18943.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1380+153T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740525 | |||||||
chr3:179740694 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1380+322G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740694 | |||||||
chr3:179740753 | C | T | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1380+381C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740753 | |||||||
chr3:179740769 | CT | C | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0002g0036 others(3): Show |
6 | HG01169.hp2 HG01975.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1380+412delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr3 | 179740769 | ||||||
chr3:179740827 | C | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1380+455C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740827 | |||||||
chr3:179740869 | C | T | 1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1380+497C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740869 | |||||||
chr3:179740913 | C | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1380+541C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740913 | |||||||
chr3:179740923 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1380+551C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740923 | |||||||
chr3:179740924 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(45): Show |
48 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1380+552G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740924 | |||||||
chr3:179740945 | T | G | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1380+573T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740945 | |||||||
chr3:179740979 | C | T | 2 | a0003c0010t0009g0069 a0003c0010t0009g0102 |
2 | HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1380+607C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179740979 | |||||||
chr3:179741017 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1380+645G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741017 | |||||||
chr3:179741047 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1380+675G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741047 | |||||||
chr3:179741113 | C | G | 2 | a0001c0001t0004g0261 a0001c0002t0004g0186 |
2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1380+741C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741113 | |||||||
chr3:179741349 | AC | A | 51 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(48): Show |
52 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1381-847delC | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741349 | |||||||
chr3:179741407 | A | C | 1 | a0001c0001t0023g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1381-790A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741407 | |||||||
chr3:179741511 | T | C | 236 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(233): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1381-686T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741511 | |||||||
chr3:179741521 | AT | A | 243 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(240): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1381-669delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr3 | 179741521 | ||||||
chr3:179741545 | C | T | 1 | a0001c0001t0012g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1381-652C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741545 | |||||||
chr3:179741577 | G | A | 1 | a0001c0001t0006g0081 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1381-620G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741577 | |||||||
chr3:179741599 | C | T | 1 | a0001c0005t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1381-598C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741599 | |||||||
chr3:179741600 | A | G | 243 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(240): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1381-597A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741600 | |||||||
chr3:179741694 | A | G | 127 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1381-503A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179741694 | |||||||
chr3:179742085 | G | A | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1381-112G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 11/20 | chr3 | 179742085 | |||||||
chr3:179742447 | G | C | 1 | a0001c0001t0037g0029 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1534+97G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179742447 | |||||||
chr3:179742510 | G | C | 12 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1534+160G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179742510 | |||||||
chr3:179742552 | A | T | 51 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0279 others(48): Show |
52 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1534+202A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179742552 | |||||||
chr3:179742563 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1534+213A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179742563 | |||||||
chr3:179742955 | T | C | 12 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(9): Show |
12 | HG00140.hp2 HG01099.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1534+605T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179742955 | |||||||
chr3:179743037 | T | C | 158 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0043 others(155): Show |
159 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1534+687T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743037 | |||||||
chr3:179743161 | C | A | 33 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0075 others(30): Show |
33 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.1534+811C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743161 | |||||||
chr3:179743180 | C | T | 19 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(16): Show |
19 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1534+830C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743180 | |||||||
chr3:179743258 | G | T | 1 | a0001c0002t0001g0131 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1534+908G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743258 | |||||||
chr3:179743346 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0030 others(38): Show |
41 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1534+996G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743346 | |||||||
chr3:179743389 | T | G | 70 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(67): Show |
70 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1534+1039T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743389 | |||||||
chr3:179743456 | T | G | 67 | a0001c0001t0001g0030 a0001c0001t0001g0043 a0001c0001t0001g0048 others(64): Show |
67 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1534+1106T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743456 | |||||||
chr3:179743462 | G | T | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1534+1112G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743462 | |||||||
chr3:179743522 | C | T | 3 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0054 |
3 | HG01123.hp2 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1534+1172C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743522 | |||||||
chr3:179743526 | T | G | 1 | a0001c0001t0002g0114 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1534+1176T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743526 | |||||||
chr3:179743652 | G | A | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1534+1302G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743652 | |||||||
chr3:179743652 | G | C | 15 | a0001c0001t0001g0287 a0001c0001t0005g0017 a0001c0001t0005g0202 others(12): Show |
15 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1534+1302G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743652 | |||||||
chr3:179743684 | T | G | 130 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(127): Show |
131 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1534+1334T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743684 | |||||||
chr3:179743830 | CTGAT | C | 108 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(105): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1535-1210_1535-120 others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179743830 | ||||||
chr3:179743846 | G | T | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1535-1197G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743846 | |||||||
chr3:179743895 | G | A | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1535-1148G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743895 | |||||||
chr3:179743905 | C | T | 147 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(144): Show |
148 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.1535-1138C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743905 | |||||||
chr3:179743922 | A | C | 2 | a0001c0001t0009g0101 a0001c0002t0009g0141 |
2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1535-1121A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743922 | |||||||
chr3:179743926 | G | GT | 126 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0048 others(123): Show |
126 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1535-1098dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179743926 | ||||||
chr3:179743926 | G | GTT | 22 | a0001c0001t0001g0025 a0001c0001t0001g0075 a0001c0001t0001g0108 others(19): Show |
22 | HG00741.hp2 HG01175.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1535-1099_1535-109 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179743926 | ||||||
chr3:179743926 | G | GTTT | 38 | a0001c0001t0001g0203 a0001c0001t0001g0221 a0001c0001t0001g0251 others(35): Show |
38 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1535-1100_1535-109 others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179743926 | ||||||
chr3:179743926 | G | GTTTT | 7 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(4): Show |
7 | HG01934.hp1 HG02129.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1535-1101_1535-109 others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179743926 | ||||||
chr3:179743926 | GT | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0030 others(45): Show |
48 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1535-1098delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179743926 | ||||||
chr3:179743926 | GTT | G | 10 | a0001c0001t0001g0094 a0001c0001t0004g0018 a0001c0001t0004g0234 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1535-1099_1535-109 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179743926 | ||||||
chr3:179743989 | A | G | 1 | a0001c0009t0005g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1535-1054A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179743989 | |||||||
chr3:179744294 | A | G | 1 | a0001c0001t0010g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1535-749A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744294 | |||||||
chr3:179744298 | T | C | 1 | a0001c0006t0001g0153 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1535-745T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744298 | |||||||
chr3:179744343 | GT | G | 46 | a0001c0001t0001g0068 a0001c0001t0001g0207 a0001c0001t0001g0211 others(43): Show |
47 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1535-689delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179744343 | ||||||
chr3:179744349 | TTTTTTGT others(9): Show |
T | 3 | a0001c0001t0001g0287 a0001c0001t0006g0240 a0001c0001t0006g0288 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1535-688_1535-673d others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179744349 | ||||||
chr3:179744353 | TTG | T | 14 | a0001c0001t0001g0260 a0001c0001t0005g0017 a0001c0001t0005g0202 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1535-688_1535-687d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr3 | 179744353 | ||||||
chr3:179744354 | TG | T | 55 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0058 others(52): Show |
55 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1535-688delG | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744354 | |||||||
chr3:179744355 | G | T | 7 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0225 others(4): Show |
7 | HG01175.hp1 HG01993.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1535-688G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744355 | |||||||
chr3:179744356 | T | G | 3 | a0001c0001t0001g0260 a0001c0001t0017g0192 a0001c0002t0001g0185 |
3 | HG02486.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1535-687T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744356 | |||||||
chr3:179744359 | T | G | 12 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1535-684T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744359 | |||||||
chr3:179744360 | G | T | 12 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1535-683G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744360 | |||||||
chr3:179744365 | G | T | 21 | a0001c0001t0001g0260 a0001c0001t0004g0018 a0001c0001t0004g0234 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1535-678G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744365 | |||||||
chr3:179744545 | C | A | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1535-498C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744545 | |||||||
chr3:179744621 | G | A | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1535-422G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744621 | |||||||
chr3:179744918 | A | G | 4 | a0001c0008t0004g0264 a0001c0008t0008g0237 a0001c0008t0008g0265 others(1): Show |
4 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535-125A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744918 | |||||||
chr3:179744955 | C | G | 14 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1535-88C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179744955 | |||||||
chr3:179745007 | G | A | 1 | a0001c0001t0007g0013 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1535-36G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 12/20 | chr3 | 179745007 | |||||||
chr3:179745288 | A | G | 208 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0048 others(205): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1709+71A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745288 | |||||||
chr3:179745293 | G | A | 137 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(134): Show |
138 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1709+76G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745293 | |||||||
chr3:179745313 | G | T | 5 | a0001c0001t0003g0299 a0001c0003t0005g0002 a0001c0003t0005g0242 others(2): Show |
5 | HG02559.hp1 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1709+96G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745313 | |||||||
chr3:179745335 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1709+118T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745335 | |||||||
chr3:179745354 | C | T | 1 | a0001c0002t0006g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1709+137C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745354 | |||||||
chr3:179745368 | C | T | 11 | a0001c0002t0001g0134 a0001c0003t0001g0230 a0001c0003t0001g0255 others(8): Show |
11 | HG01255.hp2 HG01433.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1709+151C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745368 | |||||||
chr3:179745421 | A | G | 1 | a0001c0001t0005g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1709+204A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745421 | |||||||
chr3:179745425 | C | T | 1 | a0001c0002t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1709+208C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745425 | |||||||
chr3:179745461 | A | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0002g0024 others(5): Show |
8 | HG00597.hp2 HG00642.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1709+244A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745461 | |||||||
chr3:179745492 | G | GCCTT | 70 | a0001c0001t0001g0211 a0001c0001t0001g0218 a0001c0001t0001g0222 others(67): Show |
71 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1709+296_1709+299d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179745492 | ||||||
chr3:179745501 | CCTTCCTT others(21): Show |
C | 5 | a0001c0001t0006g0297 a0001c0002t0001g0139 a0001c0002t0004g0170 others(2): Show |
5 | HG01109.hp1 HG02896.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1709+300_1709+327d others(30): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179745501 | ||||||
chr3:179745505 | C | T | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1709+288C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745505 | |||||||
chr3:179745529 | T | TCTTTCTT others(5): Show |
1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1709+315_1709+316i others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179745529 | ||||||
chr3:179745533 | C | T | 5 | a0001c0001t0004g0018 a0001c0001t0004g0234 a0001c0001t0008g0040 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1709+316C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745533 | |||||||
chr3:179745711 | A | G | 1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1709+494A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745711 | |||||||
chr3:179745741 | C | G | 2 | a0001c0002t0040g0126 a0001c0002t0043g0125 |
2 | NA18966.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1709+524C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745741 | |||||||
chr3:179745871 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1709+654T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745871 | |||||||
chr3:179745913 | G | A | 200 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0048 others(197): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1709+696G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179745913 | |||||||
chr3:179746048 | C | G | 1 | a0001c0001t0015g0292 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1709+831C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746048 | |||||||
chr3:179746171 | T | G | 6 | a0001c0001t0008g0198 a0001c0001t0015g0292 a0001c0001t0024g0235 others(3): Show |
6 | HG00735.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1709+954T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746171 | |||||||
chr3:179746191 | A | G | 1 | a0001c0002t0001g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1709+974A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746191 | |||||||
chr3:179746268 | T | A | 210 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(207): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1709+1051T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746268 | |||||||
chr3:179746310 | G | A | 121 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(118): Show |
122 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1709+1093G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746310 | |||||||
chr3:179746414 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1709+1197C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746414 | |||||||
chr3:179746432 | T | A | 113 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(110): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1709+1215T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746432 | |||||||
chr3:179746441 | T | G | 1 | a0001c0001t0003g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1709+1224T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746441 | |||||||
chr3:179746506 | T | C | 276 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(273): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1709+1289T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746506 | |||||||
chr3:179746507 | G | A | 1 | a0001c0003t0039g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1709+1290G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746507 | |||||||
chr3:179746510 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1709+1293A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746510 | |||||||
chr3:179746605 | T | C | 122 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(119): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1709+1388T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746605 | |||||||
chr3:179746711 | A | G | 138 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(135): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1709+1494A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746711 | |||||||
chr3:179746784 | G | C | 122 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(119): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1709+1567G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746784 | |||||||
chr3:179746896 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1709+1679C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179746896 | |||||||
chr3:179747281 | A | G | 2 | a0001c0003t0005g0002 a0001c0003t0005g0242 |
2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1709+2064A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747281 | |||||||
chr3:179747444 | G | C | 14 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1709+2227G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747444 | |||||||
chr3:179747518 | C | G | 8 | a0001c0001t0004g0261 a0001c0002t0004g0143 a0001c0002t0004g0186 others(5): Show |
8 | HG02630.hp2 HG02647.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1709+2301C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747518 | |||||||
chr3:179747753 | C | G | 1 | a0001c0002t0001g0131 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1709+2536C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747753 | |||||||
chr3:179747755 | A | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0234 a0001c0001t0008g0040 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1709+2538A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747755 | |||||||
chr3:179747838 | A | G | 138 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(135): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1709+2621A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747838 | |||||||
chr3:179747850 | G | C | 138 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(135): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1709+2633G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747850 | |||||||
chr3:179747861 | T | G | 14 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1709+2644T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747861 | |||||||
chr3:179747869 | C | G | 14 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1709+2652C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747869 | |||||||
chr3:179747871 | T | C | 11 | a0001c0002t0001g0134 a0001c0003t0001g0230 a0001c0003t0001g0255 others(8): Show |
11 | HG01255.hp2 HG01433.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1709+2654T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747871 | |||||||
chr3:179747902 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1709+2685C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747902 | |||||||
chr3:179747925 | C | G | 1 | a0001c0001t0001g0051 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1709+2708C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747925 | |||||||
chr3:179747970 | T | C | 152 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(149): Show |
153 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1709+2753T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179747970 | |||||||
chr3:179748259 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1709+3042C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179748259 | |||||||
chr3:179748350 | T | C | 1 | a0001c0001t0005g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1709+3133T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179748350 | |||||||
chr3:179748723 | T | C | 1 | a0001c0001t0009g0103 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1709+3506T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179748723 | |||||||
chr3:179748896 | A | T | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1710-3389A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179748896 | |||||||
chr3:179749035 | T | A | 1 | a0001c0002t0040g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1710-3250T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179749035 | |||||||
chr3:179749072 | C | A | 6 | a0001c0001t0001g0287 a0001c0001t0004g0018 a0001c0001t0004g0234 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1710-3213C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179749072 | |||||||
chr3:179749091 | T | C | 6 | a0001c0001t0001g0287 a0001c0001t0004g0018 a0001c0001t0004g0234 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1710-3194T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179749091 | |||||||
chr3:179749224 | A | C | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1710-3061A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179749224 | |||||||
chr3:179749298 | A | C | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1710-2987A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179749298 | |||||||
chr3:179749389 | A | G | 1 | a0001c0001t0003g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1710-2896A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179749389 | |||||||
chr3:179749673 | A | G | 11 | a0001c0002t0001g0134 a0001c0003t0001g0230 a0001c0003t0001g0255 others(8): Show |
11 | HG01255.hp2 HG01433.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1710-2612A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179749673 | |||||||
chr3:179750189 | C | T | 3 | a0002c0007t0001g0200 a0002c0007t0001g0243 a0002c0007t0001g0253 |
3 | NA18947.hp2 NA18950.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1710-2096C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750189 | |||||||
chr3:179750213 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1710-2072C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750213 | |||||||
chr3:179750291 | T | C | 1 | a0001c0001t0023g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1710-1994T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750291 | |||||||
chr3:179750296 | A | G | 1 | a0001c0002t0001g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1710-1989A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750296 | |||||||
chr3:179750296 | ATG | A | 9 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0002g0024 others(6): Show |
9 | HG00597.hp2 HG00642.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1710-1981_1710-198 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750296 | ||||||
chr3:179750298 | GTGTGTGT others(15): Show |
G | 48 | a0001c0001t0001g0095 a0001c0001t0001g0207 a0001c0001t0001g0211 others(45): Show |
49 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1710-1963_1710-194 others(26): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750298 | ||||||
chr3:179750302 | GTGTATAT others(23): Show |
G | 14 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1710-1981_1710-195 others(34): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750302 | ||||||
chr3:179750302 | GTGTATAT others(29): Show |
G | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1710-1981_1710-194 others(40): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750302 | ||||||
chr3:179750304 | G | A | 120 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1710-1981G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750304 | |||||||
chr3:179750304 | G | GTA | 40 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(37): Show |
40 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1710-1965_1710-196 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750304 | ||||||
chr3:179750304 | G | GTATATAT others(25): Show |
1 | a0001c0001t0001g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1710-1964_1710-196 others(36): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750304 | ||||||
chr3:179750304 | GTATATAT others(17): Show |
G | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1710-1961_1710-193 others(28): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750304 | ||||||
chr3:179750306 | A | G | 5 | a0001c0001t0003g0299 a0001c0003t0005g0002 a0001c0003t0005g0242 others(2): Show |
5 | HG02559.hp1 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1710-1979A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750306 | |||||||
chr3:179750306 | ATATATAT others(13): Show |
A | 59 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(56): Show |
59 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1710-1963_1710-194 others(24): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750306 | ||||||
chr3:179750308 | ATATATAT others(11): Show |
A | 3 | a0001c0001t0001g0063 a0001c0001t0011g0252 a0004c0013t0001g0010 |
3 | HG02735.hp2 NA18612.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1710-1963_1710-194 others(22): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750308 | ||||||
chr3:179750312 | A | ATATATGT others(3): Show |
1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1710-1968_1710-196 others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750312 | ||||||
chr3:179750312 | ATATATAT others(7): Show |
A | 9 | a0001c0001t0003g0299 a0001c0003t0001g0230 a0001c0003t0001g0255 others(6): Show |
9 | HG01433.hp1 HG02257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1710-1963_1710-195 others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750312 | ||||||
chr3:179750314 | ATATATAT others(5): Show |
A | 5 | a0001c0003t0001g0290 a0001c0005t0001g0142 a0001c0005t0001g0150 others(2): Show |
5 | HG01255.hp2 HG01891.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1710-1963_1710-195 others(16): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750314 | ||||||
chr3:179750316 | ATATATGT others(3): Show |
A | 2 | a0001c0002t0001g0134 a0001c0005t0001g0188 |
2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1710-1963_1710-195 others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750316 | ||||||
chr3:179750318 | A | G | 1 | a0001c0001t0008g0293 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1710-1967A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750318 | |||||||
chr3:179750320 | A | ATATATAT others(3): Show |
2 | a0001c0002t0016g0173 a0001c0002t0033g0174 |
2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1710-1964_1710-196 others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750320 | ||||||
chr3:179750320 | A | ATATG | 5 | a0001c0001t0006g0297 a0001c0002t0001g0139 a0001c0002t0004g0170 others(2): Show |
5 | HG01109.hp1 HG02896.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1710-1964_1710-196 others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750320 | ||||||
chr3:179750320 | A | ATATGTG | 4 | a0001c0001t0004g0261 a0001c0002t0004g0186 a0001c0006t0004g0179 others(1): Show |
4 | HG02970.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1710-1964_1710-196 others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750320 | ||||||
chr3:179750320 | A | G | 4 | a0001c0001t0003g0118 a0001c0001t0008g0293 a0001c0002t0003g0158 others(1): Show |
4 | HG01169.hp1 HG02647.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1710-1965A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750320 | |||||||
chr3:179750322 | G | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0080 others(7): Show |
10 | HG00642.hp1 HG01169.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.1710-1963G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750322 | |||||||
chr3:179750322 | GTGTGTAT others(13): Show |
G | 9 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0002g0024 others(6): Show |
9 | HG00597.hp2 HG00642.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1710-1961_1710-194 others(24): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750322 | ||||||
chr3:179750324 | G | A | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1710-1961G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750324 | |||||||
chr3:179750326 | G | A | 55 | a0001c0001t0001g0095 a0001c0001t0001g0207 a0001c0001t0001g0211 others(52): Show |
56 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.1710-1959G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750326 | |||||||
chr3:179750326 | G | GTA | 3 | a0001c0001t0001g0078 a0001c0001t0001g0245 a0003c0010t0009g0069 |
3 | HG04204.hp2 NA18950.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1710-1941_1710-194 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTATATA | 4 | a0001c0001t0008g0293 a0001c0008t0004g0264 a0001c0008t0008g0265 others(1): Show |
4 | HG01169.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1710-1945_1710-194 others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTATATAT others(13): Show |
2 | a0001c0001t0022g0257 a0001c0012t0004g0289 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1710-1940_1710-193 others(24): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1710-1940_1710-193 others(28): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTATAT others(3): Show |
1 | a0001c0002t0003g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1710-1958_1710-195 others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTATAT others(5): Show |
1 | a0001c0001t0002g0256 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1710-1958_1710-195 others(16): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTATAT others(7): Show |
10 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0037g0029 others(7): Show |
10 | HG00140.hp2 HG01099.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1710-1958_1710-195 others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTATAT others(11): Show |
1 | a0001c0001t0002g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1710-1958_1710-195 others(22): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTATAT others(15): Show |
1 | a0001c0001t0003g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1710-1958_1710-195 others(26): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTGTAT others(3): Show |
1 | a0001c0001t0003g0294 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1710-1958_1710-195 others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTGTAT others(7): Show |
1 | a0001c0001t0023g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1710-1958_1710-195 others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTGTAT others(13): Show |
1 | a0001c0001t0003g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1710-1958_1710-195 others(24): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTGTAT others(17): Show |
2 | a0001c0001t0001g0251 a0001c0001t0003g0090 |
2 | HG02074.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1710-1958_1710-195 others(28): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTGTAT others(19): Show |
7 | a0001c0001t0001g0075 a0001c0001t0003g0009 a0001c0001t0003g0021 others(4): Show |
7 | HG01975.hp2 HG02015.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1710-1958_1710-195 others(30): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTGTAT others(21): Show |
7 | a0001c0001t0003g0022 a0001c0001t0003g0028 a0001c0001t0003g0042 others(4): Show |
7 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1710-1958_1710-195 others(32): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTGTAT others(23): Show |
2 | a0001c0001t0001g0221 a0001c0001t0003g0026 |
2 | HG01934.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1710-1958_1710-195 others(34): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750326 | G | GTGTGTGT others(27): Show |
1 | a0001c0001t0003g0208 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1710-1958_1710-195 others(38): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr3 | 179750326 | ||||||
chr3:179750328 | A | G | 12 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0079 others(9): Show |
12 | HG00642.hp1 HG01169.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.1710-1957A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750328 | |||||||
chr3:179750346 | G | A | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1710-1939G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750346 | |||||||
chr3:179750475 | A | G | 1 | a0001c0003t0005g0242 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1710-1810A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750475 | |||||||
chr3:179750597 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0278 |
2 | HG01952.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1710-1688A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750597 | |||||||
chr3:179750632 | A | G | 1 | a0001c0001t0003g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1710-1653A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750632 | |||||||
chr3:179750637 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1710-1648A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750637 | |||||||
chr3:179750740 | C | T | 64 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(61): Show |
64 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1710-1545C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750740 | |||||||
chr3:179750877 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1710-1408A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750877 | |||||||
chr3:179750990 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1710-1295A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179750990 | |||||||
chr3:179751090 | A | G | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1710-1195A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179751090 | |||||||
chr3:179751119 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1710-1166C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179751119 | |||||||
chr3:179751157 | A | G | 199 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(196): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.1710-1128A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179751157 | |||||||
chr3:179751362 | T | C | 1 | a0001c0004t0006g0226 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1710-923T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179751362 | |||||||
chr3:179751915 | G | T | 1 | a0001c0002t0003g0180 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1710-370G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179751915 | |||||||
chr3:179751995 | G | A | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1710-290G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179751995 | |||||||
chr3:179752058 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1710-227C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179752058 | |||||||
chr3:179752058 | C | T | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1710-227C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179752058 | |||||||
chr3:179752101 | A | G | 1 | a0001c0004t0034g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1710-184A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179752101 | |||||||
chr3:179752180 | A | T | 1 | a0001c0001t0011g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1710-105A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179752180 | |||||||
chr3:179752207 | A | G | 63 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(60): Show |
63 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1710-78A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 13/20 | chr3 | 179752207 | |||||||
chr3:179752389 | G | T | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1798+16G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179752389 | |||||||
chr3:179752411 | A | G | 1 | a0001c0002t0004g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1798+38A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179752411 | |||||||
chr3:179752587 | C | T | 64 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(61): Show |
64 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1798+214C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179752587 | |||||||
chr3:179752733 | T | G | 1 | a0001c0004t0012g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1798+360T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179752733 | |||||||
chr3:179752858 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1798+485G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179752858 | |||||||
chr3:179752960 | G | A | 3 | a0001c0001t0002g0216 a0001c0001t0035g0056 a0001c0002t0041g0124 |
3 | NA18949.hp2 NA18967.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1798+587G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179752960 | |||||||
chr3:179753071 | A | G | 122 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(119): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1798+698A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179753071 | |||||||
chr3:179753183 | C | T | 4 | a0001c0004t0002g0182 a0001c0004t0002g0267 a0001c0006t0001g0153 others(1): Show |
4 | HG02683.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1798+810C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179753183 | |||||||
chr3:179753225 | A | T | 3 | a0001c0002t0004g0143 a0001c0002t0016g0173 a0001c0002t0033g0174 |
3 | HG02630.hp2 HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1798+852A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179753225 | |||||||
chr3:179753234 | C | T | 1 | a0001c0001t0023g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1798+861C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179753234 | |||||||
chr3:179753585 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1799-1147T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179753585 | |||||||
chr3:179753768 | C | G | 1 | a0001c0002t0003g0180 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1799-964C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179753768 | |||||||
chr3:179753847 | C | T | 1 | a0001c0002t0004g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1799-885C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179753847 | |||||||
chr3:179753984 | A | G | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1799-748A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179753984 | |||||||
chr3:179754031 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1799-701A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754031 | |||||||
chr3:179754041 | G | A | 5 | a0001c0001t0004g0018 a0001c0001t0004g0234 a0001c0001t0008g0040 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1799-691G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754041 | |||||||
chr3:179754046 | G | A | 4 | a0001c0003t0005g0002 a0001c0003t0005g0242 a0001c0005t0005g0122 others(1): Show |
4 | HG02559.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1799-686G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754046 | |||||||
chr3:179754157 | G | C | 119 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0058 others(116): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1799-575G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754157 | |||||||
chr3:179754223 | TATG | T | 9 | a0001c0001t0004g0261 a0001c0002t0004g0143 a0001c0002t0004g0186 others(6): Show |
9 | HG02615.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1799-505_1799-503d others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr3 | 179754223 | ||||||
chr3:179754225 | T | C | 1 | a0001c0001t0008g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1799-507T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754225 | |||||||
chr3:179754331 | G | A | 1 | a0001c0001t0011g0065 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1799-401G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754331 | |||||||
chr3:179754333 | G | A | 1 | a0001c0001t0011g0065 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1799-399G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754333 | |||||||
chr3:179754576 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0031g0227 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1799-156T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754576 | |||||||
chr3:179754599 | G | A | 4 | a0001c0003t0005g0002 a0001c0003t0005g0242 a0001c0005t0005g0122 others(1): Show |
4 | HG02559.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1799-133G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754599 | |||||||
chr3:179754599 | G | C | 14 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1799-133G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 14/20 | chr3 | 179754599 | |||||||
chr3:179754859 | C | T | 1 | a0001c0001t0006g0273 | 1 | HG00741.hp1 | splice_region_variant&intron_variant | LOW | c.1921+5C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179754859 | |||||||
chr3:179754872 | G | A | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1921+18G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179754872 | |||||||
chr3:179754886 | C | T | 132 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0058 others(129): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1921+32C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179754886 | |||||||
chr3:179755080 | G | A | 132 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0058 others(129): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1921+226G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755080 | |||||||
chr3:179755146 | A | G | 1 | a0001c0001t0007g0106 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1921+292A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755146 | |||||||
chr3:179755213 | T | G | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1921+359T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755213 | |||||||
chr3:179755223 | A | T | 132 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0058 others(129): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1921+369A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755223 | |||||||
chr3:179755322 | C | T | 2 | a0001c0001t0014g0184 a0001c0001t0014g0276 |
2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1921+468C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755322 | |||||||
chr3:179755358 | G | A | 17 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(14): Show |
17 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1921+504G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755358 | |||||||
chr3:179755441 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1921+587C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755441 | |||||||
chr3:179755559 | A | G | 17 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0213 others(14): Show |
17 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1921+705A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755559 | |||||||
chr3:179755577 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1921+723C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755577 | |||||||
chr3:179755587 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1921+733T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755587 | |||||||
chr3:179755784 | C | T | 2 | a0001c0001t0001g0260 a0001c0002t0001g0185 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1921+930C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755784 | |||||||
chr3:179755932 | C | T | 44 | a0001c0001t0001g0203 a0001c0001t0002g0256 a0001c0001t0003g0294 others(41): Show |
44 | HG01099.hp1 HG01109.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1921+1078C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179755932 | |||||||
chr3:179756042 | A | G | 1 | a0001c0001t0009g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1922-1010A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756042 | |||||||
chr3:179756150 | C | G | 1 | a0001c0001t0003g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1922-902C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756150 | |||||||
chr3:179756260 | TA | T | 3 | a0001c0001t0003g0294 a0001c0001t0003g0299 a0001c0002t0003g0176 |
3 | HG02647.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1922-787delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr3 | 179756260 | ||||||
chr3:179756368 | G | A | 1 | a0001c0001t0031g0227 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1922-684G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756368 | |||||||
chr3:179756396 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1922-656C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756396 | |||||||
chr3:179756413 | A | AAAAC | 11 | a0001c0001t0005g0202 a0001c0001t0005g0233 a0001c0001t0005g0263 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1922-607_1922-604d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr3 | 179756413 | ||||||
chr3:179756413 | AAAAC | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(89): Show |
92 | HG00280.hp2 HG00558.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.1922-607_1922-604d others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr3 | 179756413 | ||||||
chr3:179756413 | AAAACAAA others(1): Show |
A | 20 | a0001c0001t0001g0075 a0001c0001t0003g0009 a0001c0001t0003g0021 others(17): Show |
20 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1922-611_1922-604d others(10): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr3 | 179756413 | ||||||
chr3:179756413 | AAAACAAA others(5): Show |
A | 88 | a0001c0001t0001g0218 a0001c0001t0001g0260 a0001c0001t0001g0277 others(85): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1922-615_1922-604d others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr3 | 179756413 | ||||||
chr3:179756413 | AAAACAAA others(9): Show |
A | 4 | a0001c0001t0006g0297 a0001c0002t0004g0170 a0001c0002t0006g0169 others(1): Show |
4 | HG01109.hp1 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-619_1922-604d others(18): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr3 | 179756413 | ||||||
chr3:179756517 | G | A | 89 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(86): Show |
89 | HG00280.hp2 HG00558.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.1922-535G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756517 | |||||||
chr3:179756612 | G | A | 169 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(166): Show |
170 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1922-440G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756612 | |||||||
chr3:179756690 | C | T | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1922-362C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756690 | |||||||
chr3:179756869 | G | A | 33 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(30): Show |
33 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1922-183G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756869 | |||||||
chr3:179756938 | G | T | 8 | a0001c0001t0008g0040 a0001c0001t0008g0198 a0001c0001t0008g0293 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1922-114G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756938 | |||||||
chr3:179756960 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0078 a0001c0001t0001g0082 others(1): Show |
4 | NA18950.hp2 NA19005.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1922-92A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756960 | |||||||
chr3:179756979 | A | G | 68 | a0001c0001t0001g0218 a0001c0001t0002g0003 a0001c0001t0002g0005 others(65): Show |
69 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1922-73A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179756979 | |||||||
chr3:179757031 | G | A | 1 | a0001c0003t0039g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1922-21G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 15/20 | chr3 | 179757031 | |||||||
chr3:179757193 | T | G | 4 | a0001c0001t0001g0260 a0001c0002t0001g0139 a0001c0002t0001g0177 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1948+115T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179757193 | |||||||
chr3:179757213 | G | A | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1948+135G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179757213 | |||||||
chr3:179757484 | T | C | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1948+406T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179757484 | |||||||
chr3:179757504 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0002t0001g0146 |
3 | NA18947.hp1 NA18948.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1948+426T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179757504 | |||||||
chr3:179757607 | C | G | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1948+529C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179757607 | |||||||
chr3:179757611 | G | T | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1948+533G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179757611 | |||||||
chr3:179757880 | C | G | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1948+802C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179757880 | |||||||
chr3:179758098 | C | T | 1 | a0001c0001t0013g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1948+1020C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179758098 | |||||||
chr3:179758178 | C | T | 4 | a0001c0001t0007g0268 a0001c0002t0007g0001 a0001c0002t0007g0168 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1948+1100C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179758178 | |||||||
chr3:179758179 | G | A | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1948+1101G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179758179 | |||||||
chr3:179758503 | T | A | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1948+1425T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179758503 | |||||||
chr3:179758626 | G | A | 3 | a0001c0002t0004g0172 a0001c0002t0004g0270 a0001c0004t0034g0072 |
3 | HG02280.hp1 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1948+1548G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179758626 | |||||||
chr3:179758759 | A | G | 4 | a0001c0001t0001g0260 a0001c0002t0001g0139 a0001c0002t0001g0177 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1948+1681A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179758759 | |||||||
chr3:179758793 | C | T | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1948+1715C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179758793 | |||||||
chr3:179758938 | T | C | 1 | a0001c0002t0001g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1948+1860T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179758938 | |||||||
chr3:179758939 | A | ATTCT | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1948+1863_1948+186 others(8): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr3 | 179758939 | ||||||
chr3:179759010 | G | C | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1948+1932G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179759010 | |||||||
chr3:179759271 | G | A | 1 | a0001c0002t0009g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1949-1841G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179759271 | |||||||
chr3:179759495 | A | G | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1949-1617A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179759495 | |||||||
chr3:179759527 | C | T | 17 | a0001c0001t0004g0206 a0001c0001t0005g0017 a0001c0001t0005g0202 others(14): Show |
17 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1949-1585C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179759527 | |||||||
chr3:179759559 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1949-1553T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179759559 | |||||||
chr3:179759693 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1949-1419G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179759693 | |||||||
chr3:179759785 | T | A | 3 | a0001c0002t0007g0001 a0001c0002t0007g0168 a0001c0002t0007g0175 |
4 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1949-1327T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179759785 | |||||||
chr3:179759826 | A | G | 1 | a0001c0001t0006g0273 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1949-1286A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179759826 | |||||||
chr3:179760167 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0005 others(143): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1949-945A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760167 | |||||||
chr3:179760263 | T | C | 3 | a0001c0001t0014g0184 a0001c0001t0014g0276 a0001c0001t0023g0262 |
3 | HG03130.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1949-849T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760263 | |||||||
chr3:179760282 | G | GT | 45 | a0001c0001t0001g0006 a0001c0001t0001g0108 a0001c0001t0001g0111 others(42): Show |
45 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.1949-811dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr3 | 179760282 | ||||||
chr3:179760282 | G | GTT | 21 | a0001c0001t0003g0090 a0001c0001t0004g0105 a0001c0001t0004g0236 others(18): Show |
21 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.1949-812_1949-811d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr3 | 179760282 | ||||||
chr3:179760306 | C | T | 20 | a0001c0001t0004g0018 a0001c0001t0004g0206 a0001c0001t0004g0234 others(17): Show |
20 | HG01081.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1949-806C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760306 | |||||||
chr3:179760345 | G | A | 1 | a0001c0001t0011g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1949-767G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760345 | |||||||
chr3:179760474 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1949-638G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760474 | |||||||
chr3:179760519 | A | G | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1949-593A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760519 | |||||||
chr3:179760562 | C | T | 4 | a0001c0001t0008g0040 a0001c0002t0003g0176 a0001c0002t0008g0164 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1949-550C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760562 | |||||||
chr3:179760615 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0002g0016 |
2 | HG00621.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1949-497C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760615 | |||||||
chr3:179760617 | A | C | 1 | a0001c0001t0001g0250 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1949-495A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760617 | |||||||
chr3:179760652 | C | T | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1949-460C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760652 | |||||||
chr3:179760786 | G | A | 1 | a0001c0002t0001g0159 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1949-326G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760786 | |||||||
chr3:179760937 | A | G | 2 | a0001c0001t0002g0120 a0001c0002t0002g0147 |
2 | NA18943.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1949-175A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 16/20 | chr3 | 179760937 | |||||||
chr3:179761414 | C | CT | 24 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(21): Show |
25 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2092+170dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr3 | 179761414 | ||||||
chr3:179761417 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2092+162T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179761417 | |||||||
chr3:179761508 | A | G | 145 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(142): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2092+253A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179761508 | |||||||
chr3:179761757 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2092+502C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179761757 | |||||||
chr3:179761910 | G | A | 1 | a0001c0001t0005g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2092+655G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179761910 | |||||||
chr3:179761951 | T | C | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2092+696T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179761951 | |||||||
chr3:179761952 | A | G | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2092+697A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179761952 | |||||||
chr3:179762036 | C | T | 8 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0045 others(5): Show |
8 | HG00323.hp1 HG01074.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.2092+781C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179762036 | |||||||
chr3:179762093 | T | C | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2092+838T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179762093 | |||||||
chr3:179762242 | A | C | 11 | a0001c0001t0004g0018 a0001c0001t0004g0234 a0001c0001t0008g0040 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2092+987A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179762242 | |||||||
chr3:179762335 | C | T | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2092+1080C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179762335 | |||||||
chr3:179762379 | A | G | 255 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(252): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.2092+1124A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179762379 | |||||||
chr3:179762443 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2092+1188T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179762443 | |||||||
chr3:179762589 | A | G | 8 | a0001c0001t0008g0040 a0001c0001t0008g0198 a0001c0001t0008g0293 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2092+1334A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179762589 | |||||||
chr3:179763152 | T | C | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2093-850T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179763152 | |||||||
chr3:179763307 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2093-695G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179763307 | |||||||
chr3:179763647 | T | C | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2093-355T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179763647 | |||||||
chr3:179763741 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2093-261A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179763741 | |||||||
chr3:179763742 | T | C | 129 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(126): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.2093-260T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179763742 | |||||||
chr3:179763767 | G | T | 4 | a0001c0001t0002g0117 a0001c0001t0002g0213 a0001c0001t0002g0256 others(1): Show |
4 | HG02027.hp1 HG02523.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2093-235G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179763767 | |||||||
chr3:179763827 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(98): Show |
101 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.2093-175C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | chr3 | 179763827 | |||||||
chr3:179763950 | C | CA | 22 | a0001c0001t0001g0064 a0001c0001t0001g0205 a0001c0001t0002g0038 others(19): Show |
22 | HG00438.hp2 HG02145.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.2093-33dupA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr3 | 179763950 | ||||||
chr3:179764183 | C | CTG | 16 | a0001c0001t0004g0234 a0001c0001t0006g0035 a0001c0001t0006g0081 others(13): Show |
16 | HG00140.hp2 HG00735.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2259+46_2259+47dup others(2): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr3 | 179764183 | ||||||
chr3:179764183 | CTG | C | 201 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(198): Show |
202 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.2259+46_2259+47del others(2): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr3 | 179764183 | ||||||
chr3:179764183 | CTGTG | C | 22 | a0001c0001t0001g0108 a0001c0001t0001g0217 a0001c0001t0001g0281 others(19): Show |
22 | HG00280.hp2 HG02145.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.2259+44_2259+47del others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr3 | 179764183 | ||||||
chr3:179764617 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2259+449C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | chr3 | 179764617 | |||||||
chr3:179764643 | A | C | 7 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0071 others(4): Show |
7 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.2259+475A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | chr3 | 179764643 | |||||||
chr3:179764694 | T | C | 145 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(142): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2259+526T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | chr3 | 179764694 | |||||||
chr3:179764760 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2259+592A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | chr3 | 179764760 | |||||||
chr3:179764874 | G | A | 1 | a0001c0002t0040g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2259+706G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | chr3 | 179764874 | |||||||
chr3:179765044 | A | G | 2 | a0001c0001t0017g0192 a0001c0006t0032g0140 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2260-651A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | chr3 | 179765044 | |||||||
chr3:179765133 | A | G | 1 | a0001c0001t0006g0228 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2260-562A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | chr3 | 179765133 | |||||||
chr3:179765227 | C | A | 8 | a0001c0001t0008g0040 a0001c0001t0008g0198 a0001c0001t0008g0293 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2260-468C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | chr3 | 179765227 | |||||||
chr3:179765238 | G | C | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2260-457G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 18/20 | chr3 | 179765238 | |||||||
chr3:179765977 | G | GT | 9 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0121 others(6): Show |
9 | HG02738.hp2 HG02818.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.2413+143dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179765977 | ||||||
chr3:179766048 | C | T | 1 | a0001c0001t0022g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2413+200C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766048 | |||||||
chr3:179766168 | C | T | 1 | a0001c0002t0040g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2413+320C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766168 | |||||||
chr3:179766182 | G | T | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2413+334G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766182 | |||||||
chr3:179766269 | T | C | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2413+421T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766269 | |||||||
chr3:179766419 | G | A | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2413+571G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766419 | |||||||
chr3:179766455 | A | C | 3 | a0001c0001t0003g0294 a0001c0001t0003g0299 a0001c0001t0030g0258 |
3 | HG03041.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2413+607A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766455 | |||||||
chr3:179766466 | A | G | 3 | a0001c0001t0013g0015 a0001c0001t0013g0023 a0001c0001t0019g0204 |
3 | HG03834.hp1 HG04228.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2413+618A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766466 | |||||||
chr3:179766504 | G | A | 4 | a0001c0001t0004g0018 a0001c0001t0004g0206 a0001c0001t0004g0234 others(1): Show |
4 | HG01081.hp2 HG01433.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2413+656G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766504 | |||||||
chr3:179766534 | G | A | 1 | a0001c0002t0006g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2413+686G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766534 | |||||||
chr3:179766563 | G | T | 36 | a0001c0001t0004g0018 a0001c0001t0004g0105 a0001c0001t0004g0206 others(33): Show |
36 | HG01081.hp2 HG01433.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.2413+715G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766563 | |||||||
chr3:179766777 | A | G | 4 | a0001c0002t0004g0143 a0001c0002t0004g0170 a0001c0002t0016g0173 others(1): Show |
4 | HG02630.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2413+929A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766777 | |||||||
chr3:179766868 | T | C | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2413+1020T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766868 | |||||||
chr3:179766946 | C | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0041 others(9): Show |
12 | HG00621.hp2 HG01993.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.2413+1098C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179766946 | |||||||
chr3:179767219 | G | A | 1 | a0001c0001t0010g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2413+1371G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767219 | |||||||
chr3:179767349 | G | GTAT | 4 | a0001c0001t0001g0064 a0001c0001t0001g0205 a0001c0001t0021g0295 others(1): Show |
4 | HG02055.hp2 HG06807.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2413+1501_2413+150 others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767349 | |||||||
chr3:179767352 | C | T | 6 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0054 others(3): Show |
6 | HG00323.hp1 HG01074.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2413+1504C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767352 | |||||||
chr3:179767357 | A | G | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2413+1509A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767357 | |||||||
chr3:179767427 | G | GT | 5 | a0001c0001t0008g0198 a0001c0001t0008g0293 a0001c0008t0008g0237 others(2): Show |
5 | HG01109.hp2 HG01169.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2413+1579_2413+158 others(5): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767427 | |||||||
chr3:179767427 | G | GTT | 11 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0266 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2413+1579_2413+158 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767427 | |||||||
chr3:179767427 | G | GTTT | 5 | a0001c0001t0004g0261 a0001c0002t0004g0186 a0001c0006t0004g0179 others(2): Show |
5 | HG02615.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2413+1579_2413+158 others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767427 | |||||||
chr3:179767428 | G | T | 79 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(76): Show |
79 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.2413+1580G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767428 | |||||||
chr3:179767431 | T | G | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2413+1583T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767431 | |||||||
chr3:179767445 | G | A | 3 | a0001c0001t0014g0184 a0001c0001t0014g0276 a0001c0001t0023g0262 |
3 | HG03130.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2413+1597G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767445 | |||||||
chr3:179767635 | A | T | 3 | a0001c0001t0001g0247 a0001c0002t0040g0126 a0001c0002t0043g0125 |
3 | NA18966.hp2 NA18977.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2413+1787A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767635 | |||||||
chr3:179767707 | A | T | 2 | a0001c0001t0003g0046 a0001c0001t0003g0118 |
2 | NA18945.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2413+1859A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767707 | |||||||
chr3:179767876 | A | C | 79 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(76): Show |
79 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.2413+2028A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767876 | |||||||
chr3:179767887 | C | T | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2413+2039C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179767887 | |||||||
chr3:179768152 | A | G | 1 | a0001c0001t0024g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2413+2304A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179768152 | |||||||
chr3:179768353 | C | A | 1 | a0001c0001t0002g0214 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2413+2505C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179768353 | |||||||
chr3:179768777 | C | T | 17 | a0001c0001t0004g0206 a0001c0001t0005g0017 a0001c0001t0005g0202 others(14): Show |
17 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2413+2929C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179768777 | |||||||
chr3:179768858 | A | G | 1 | a0001c0001t0022g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2413+3010A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179768858 | |||||||
chr3:179768925 | C | T | 33 | a0001c0001t0004g0105 a0001c0001t0004g0206 a0001c0001t0004g0236 others(30): Show |
33 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.2413+3077C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179768925 | |||||||
chr3:179768986 | C | T | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2413+3138C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179768986 | |||||||
chr3:179769606 | G | A | 64 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(61): Show |
65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2413+3758G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179769606 | |||||||
chr3:179769624 | G | C | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2413+3776G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179769624 | |||||||
chr3:179769700 | C | T | 3 | a0001c0002t0004g0143 a0001c0002t0016g0173 a0001c0002t0033g0174 |
3 | HG02630.hp2 HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2413+3852C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179769700 | |||||||
chr3:179769967 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2413+4119C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179769967 | |||||||
chr3:179769988 | C | G | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2413+4140C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179769988 | |||||||
chr3:179769993 | G | A | 1 | a0001c0002t0001g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2413+4145G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179769993 | |||||||
chr3:179770023 | C | T | 100 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(97): Show |
100 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.2413+4175C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770023 | |||||||
chr3:179770036 | G | A | 1 | a0001c0005t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2413+4188G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770036 | |||||||
chr3:179770109 | C | T | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2413+4261C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770109 | |||||||
chr3:179770223 | G | C | 9 | a0001c0001t0001g0211 a0001c0001t0001g0247 a0001c0001t0011g0057 others(6): Show |
9 | HG03704.hp1 NA18612.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.2413+4375G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770223 | |||||||
chr3:179770440 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2413+4592G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770440 | |||||||
chr3:179770609 | A | AT | 26 | a0001c0001t0001g0100 a0001c0001t0004g0105 a0001c0001t0004g0236 others(23): Show |
26 | HG01099.hp1 HG01109.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.2413+4775dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179770609 | ||||||
chr3:179770609 | AT | A | 17 | a0001c0001t0001g0275 a0001c0001t0005g0017 a0001c0001t0005g0202 others(14): Show |
17 | HG01169.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2413+4775delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179770609 | ||||||
chr3:179770637 | G | A | 1 | a0001c0001t0028g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2413+4789G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770637 | |||||||
chr3:179770665 | C | T | 2 | a0001c0003t0001g0230 a0001c0003t0001g0255 |
2 | HG01433.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2413+4817C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770665 | |||||||
chr3:179770691 | A | G | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2413+4843A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770691 | |||||||
chr3:179770753 | C | T | 8 | a0001c0001t0008g0040 a0001c0001t0008g0198 a0001c0001t0008g0293 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2413+4905C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770753 | |||||||
chr3:179770763 | C | G | 1 | a0001c0001t0001g0039 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2413+4915C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770763 | |||||||
chr3:179770792 | C | G | 26 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(23): Show |
26 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2413+4944C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770792 | |||||||
chr3:179770889 | A | C | 10 | a0001c0001t0006g0035 a0001c0001t0006g0081 a0001c0001t0006g0240 others(7): Show |
10 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2413+5041A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770889 | |||||||
chr3:179770918 | T | G | 10 | a0001c0001t0006g0035 a0001c0001t0006g0081 a0001c0001t0006g0240 others(7): Show |
10 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2413+5070T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179770918 | |||||||
chr3:179771006 | A | G | 51 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(48): Show |
51 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.2413+5158A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179771006 | |||||||
chr3:179771132 | C | T | 9 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2413+5284C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179771132 | |||||||
chr3:179771207 | G | A | 3 | a0001c0001t0004g0018 a0001c0001t0004g0234 a0001c0002t0004g0187 |
3 | HG01081.hp2 HG01433.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2413+5359G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179771207 | |||||||
chr3:179771591 | T | C | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2413+5743T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179771591 | |||||||
chr3:179771661 | G | A | 8 | a0001c0001t0008g0040 a0001c0001t0008g0198 a0001c0001t0008g0293 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2413+5813G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179771661 | |||||||
chr3:179771987 | T | A | 1 | a0001c0001t0002g0085 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2413+6139T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179771987 | |||||||
chr3:179772255 | C | G | 1 | a0001c0001t0002g0097 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2413+6407C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179772255 | |||||||
chr3:179772381 | C | T | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2413+6533C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179772381 | |||||||
chr3:179772570 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2413+6722G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179772570 | |||||||
chr3:179772579 | C | T | 64 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(61): Show |
65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2413+6731C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179772579 | |||||||
chr3:179772591 | A | T | 8 | a0001c0001t0008g0040 a0001c0001t0008g0198 a0001c0001t0008g0293 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2413+6743A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179772591 | |||||||
chr3:179772668 | T | G | 5 | a0001c0001t0008g0198 a0001c0001t0008g0293 a0001c0008t0008g0237 others(2): Show |
5 | HG01109.hp2 HG01169.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2413+6820T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179772668 | |||||||
chr3:179772727 | T | C | 1 | a0001c0002t0001g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2413+6879T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179772727 | |||||||
chr3:179772907 | T | A | 3 | a0001c0002t0004g0172 a0001c0002t0004g0270 a0001c0004t0034g0072 |
3 | HG02280.hp1 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2413+7059T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179772907 | |||||||
chr3:179773106 | G | A | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2413+7258G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179773106 | |||||||
chr3:179773112 | C | A | 1 | a0001c0002t0040g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2413+7264C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179773112 | |||||||
chr3:179773176 | T | C | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2413+7328T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179773176 | |||||||
chr3:179773347 | G | A | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2413+7499G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179773347 | |||||||
chr3:179773431 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2413+7583C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179773431 | |||||||
chr3:179773665 | C | T | 51 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(48): Show |
51 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.2413+7817C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179773665 | |||||||
chr3:179773669 | T | A | 3 | a0001c0001t0014g0184 a0001c0001t0014g0276 a0001c0001t0023g0262 |
3 | HG03130.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2413+7821T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179773669 | |||||||
chr3:179774155 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2414-7584A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774155 | |||||||
chr3:179774196 | T | C | 65 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(62): Show |
66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.2414-7543T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774196 | |||||||
chr3:179774238 | C | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0041 others(9): Show |
12 | HG00621.hp2 HG01993.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.2414-7501C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774238 | |||||||
chr3:179774244 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2414-7495G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774244 | |||||||
chr3:179774295 | G | A | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2414-7444G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774295 | |||||||
chr3:179774368 | T | C | 3 | a0001c0001t0004g0018 a0001c0001t0004g0234 a0001c0002t0004g0187 |
3 | HG01081.hp2 HG01433.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2414-7371T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774368 | |||||||
chr3:179774408 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0222 a0001c0001t0001g0274 others(1): Show |
4 | HG00642.hp1 HG01257.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.2414-7331G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774408 | |||||||
chr3:179774450 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2414-7289C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774450 | |||||||
chr3:179774484 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2414-7255G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774484 | |||||||
chr3:179774527 | G | GTTCCTCC others(16): Show |
5 | a0001c0001t0006g0240 a0001c0001t0006g0288 a0001c0001t0006g0297 others(2): Show |
5 | HG01109.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2414-7200_2414-719 others(27): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179774527 | ||||||
chr3:179774540 | G | A | 10 | a0001c0001t0006g0035 a0001c0001t0006g0081 a0001c0001t0006g0240 others(7): Show |
10 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2414-7199G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774540 | |||||||
chr3:179774581 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2414-7158C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774581 | |||||||
chr3:179774682 | G | A | 3 | a0001c0001t0004g0018 a0001c0001t0004g0234 a0001c0002t0004g0187 |
3 | HG01081.hp2 HG01433.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2414-7057G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774682 | |||||||
chr3:179774745 | T | C | 81 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(78): Show |
81 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.2414-6994T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774745 | |||||||
chr3:179774766 | C | A | 3 | a0001c0002t0004g0143 a0001c0002t0016g0173 a0001c0002t0033g0174 |
3 | HG02630.hp2 HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2414-6973C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774766 | |||||||
chr3:179774773 | C | A | 16 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2414-6966C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774773 | |||||||
chr3:179774841 | A | C | 1 | a0001c0001t0002g0016 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2414-6898A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774841 | |||||||
chr3:179774990 | C | T | 3 | a0001c0001t0008g0040 a0001c0002t0008g0164 a0001c0002t0008g0165 |
3 | HG01070.hp1 HG01071.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2414-6749C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179774990 | |||||||
chr3:179775267 | T | C | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2414-6472T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775267 | |||||||
chr3:179775299 | C | T | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2414-6440C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775299 | |||||||
chr3:179775310 | C | A | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6429C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775310 | |||||||
chr3:179775318 | G | C | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6421G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775318 | |||||||
chr3:179775321 | A | ATGTAGTG others(33): Show |
1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6418_2414-641 others(44): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775321 | |||||||
chr3:179775323 | A | G | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6416A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775323 | |||||||
chr3:179775324 | C | T | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6415C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775324 | |||||||
chr3:179775326 | C | G | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6413C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775326 | |||||||
chr3:179775327 | A | G | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6412A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775327 | |||||||
chr3:179775329 | A | T | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6410A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775329 | |||||||
chr3:179775332 | A | T | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6407A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775332 | |||||||
chr3:179775333 | C | A | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6406C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775333 | |||||||
chr3:179775334 | T | G | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6405T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775334 | |||||||
chr3:179775341 | TGCATCCA others(19): Show |
T | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6397_2414-637 others(30): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775341 | |||||||
chr3:179775482 | G | A | 1 | a0001c0001t0003g0299 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2414-6257G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775482 | |||||||
chr3:179775497 | C | G | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-6242C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775497 | |||||||
chr3:179775704 | A | G | 258 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2414-6035A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775704 | |||||||
chr3:179775724 | G | A | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2414-6015G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775724 | |||||||
chr3:179775769 | C | T | 20 | a0001c0001t0004g0018 a0001c0001t0004g0206 a0001c0001t0004g0234 others(17): Show |
20 | HG01081.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2414-5970C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775769 | |||||||
chr3:179775825 | G | T | 20 | a0001c0001t0004g0018 a0001c0001t0004g0206 a0001c0001t0004g0234 others(17): Show |
20 | HG01081.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2414-5914G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775825 | |||||||
chr3:179775826 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2414-5913C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775826 | |||||||
chr3:179775840 | G | A | 14 | a0001c0001t0002g0024 a0001c0001t0002g0037 a0001c0001t0002g0089 others(11): Show |
14 | HG00642.hp2 HG02027.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.2414-5899G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775840 | |||||||
chr3:179775846 | G | C | 10 | a0001c0001t0006g0035 a0001c0001t0006g0081 a0001c0001t0006g0240 others(7): Show |
10 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2414-5893G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775846 | |||||||
chr3:179775866 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2414-5873C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775866 | |||||||
chr3:179775945 | G | A | 64 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(61): Show |
65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2414-5794G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775945 | |||||||
chr3:179775960 | C | CAGGGAAG others(3): Show |
1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5779_2414-577 others(14): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775960 | |||||||
chr3:179775963 | C | A | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5776C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775963 | |||||||
chr3:179775999 | T | A | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5740T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179775999 | |||||||
chr3:179776030 | T | G | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5709T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776030 | |||||||
chr3:179776031 | G | T | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5708G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776031 | |||||||
chr3:179776032 | T | C | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5707T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776032 | |||||||
chr3:179776041 | ACCACCAG others(9): Show |
A | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5694_2414-567 others(20): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179776041 | ||||||
chr3:179776089 | T | G | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5650T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776089 | |||||||
chr3:179776090 | T | A | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5649T>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776090 | |||||||
chr3:179776092 | G | T | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5647G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776092 | |||||||
chr3:179776094 | A | G | 1 | a0001c0001t0038g0008 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414-5645A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776094 | |||||||
chr3:179776202 | A | G | 16 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2414-5537A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776202 | |||||||
chr3:179776265 | T | C | 1 | a0001c0001t0004g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2414-5474T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776265 | |||||||
chr3:179776424 | G | A | 2 | a0001c0001t0017g0192 a0001c0006t0032g0140 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2414-5315G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776424 | |||||||
chr3:179776588 | CAGA | C | 3 | a0001c0002t0004g0172 a0001c0002t0004g0270 a0001c0004t0034g0072 |
3 | HG02280.hp1 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2414-5150_2414-514 others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776588 | |||||||
chr3:179776858 | G | GT | 108 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0041 others(105): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.2414-4856dupT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179776858 | ||||||
chr3:179776858 | G | GTT | 36 | a0001c0001t0002g0024 a0001c0001t0002g0074 a0001c0001t0002g0097 others(33): Show |
36 | HG00323.hp1 HG00597.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.2414-4857_2414-485 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179776858 | ||||||
chr3:179776858 | G | GTTT | 7 | a0001c0001t0003g0118 a0001c0001t0003g0294 a0001c0001t0003g0299 others(4): Show |
7 | HG02145.hp2 HG02647.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2414-4858_2414-485 others(7): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179776858 | ||||||
chr3:179776858 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0002g0007 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2414-4866_2414-485 others(15): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179776858 | ||||||
chr3:179776858 | GT | G | 22 | a0001c0001t0001g0034 a0001c0001t0001g0048 a0001c0001t0001g0058 others(19): Show |
22 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2414-4856delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179776858 | ||||||
chr3:179776886 | G | T | 1 | a0001c0001t0002g0007 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2414-4853G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179776886 | |||||||
chr3:179777003 | T | C | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2414-4736T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777003 | |||||||
chr3:179777252 | T | C | 1 | a0001c0001t0017g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2414-4487T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777252 | |||||||
chr3:179777279 | A | G | 4 | a0001c0001t0007g0268 a0001c0002t0007g0001 a0001c0002t0007g0168 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.2414-4460A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777279 | |||||||
chr3:179777337 | T | G | 5 | a0001c0001t0008g0198 a0001c0001t0008g0293 a0001c0008t0008g0237 others(2): Show |
5 | HG01109.hp2 HG01169.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2414-4402T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777337 | |||||||
chr3:179777443 | CT | C | 229 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(226): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.2414-4276delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179777443 | ||||||
chr3:179777443 | CTT | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0207 a0001c0001t0001g0275 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2414-4277_2414-427 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179777443 | ||||||
chr3:179777446 | T | C | 26 | a0001c0001t0002g0054 a0001c0001t0003g0009 a0001c0001t0003g0021 others(23): Show |
26 | HG01123.hp2 HG01255.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2414-4293T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777446 | |||||||
chr3:179777578 | G | C | 3 | a0001c0001t0008g0040 a0001c0002t0008g0164 a0001c0002t0008g0165 |
3 | HG01070.hp1 HG01071.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2414-4161G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777578 | |||||||
chr3:179777592 | A | G | 20 | a0001c0001t0004g0018 a0001c0001t0004g0206 a0001c0001t0004g0234 others(17): Show |
20 | HG01081.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2414-4147A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777592 | |||||||
chr3:179777691 | A | G | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2414-4048A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777691 | |||||||
chr3:179777704 | G | A | 16 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2414-4035G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777704 | |||||||
chr3:179777771 | T | C | 20 | a0001c0001t0004g0018 a0001c0001t0004g0206 a0001c0001t0004g0234 others(17): Show |
20 | HG01081.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2414-3968T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777771 | |||||||
chr3:179777829 | A | G | 10 | a0001c0001t0006g0035 a0001c0001t0006g0081 a0001c0001t0006g0240 others(7): Show |
10 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2414-3910A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777829 | |||||||
chr3:179777854 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2414-3885A>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777854 | |||||||
chr3:179777859 | A | G | 9 | a0001c0001t0004g0261 a0001c0002t0004g0143 a0001c0002t0004g0170 others(6): Show |
9 | HG02615.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2414-3880A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777859 | |||||||
chr3:179777869 | A | G | 26 | a0001c0001t0004g0105 a0001c0001t0004g0236 a0001c0001t0004g0261 others(23): Show |
26 | HG00140.hp2 HG01099.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2414-3870A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179777869 | |||||||
chr3:179778108 | A | C | 1 | a0001c0008t0004g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2414-3631A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778108 | |||||||
chr3:179778237 | A | C | 10 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0045 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(7): Show |
intron_variant | MODIFIER | c.2414-3502A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778237 | |||||||
chr3:179778441 | A | G | 1 | a0001c0001t0006g0288 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2414-3298A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778441 | |||||||
chr3:179778455 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2414-3284C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778455 | |||||||
chr3:179778567 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0108 a0001c0001t0001g0217 others(1): Show |
4 | HG02165.hp2 NA19002.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.2414-3172C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778567 | |||||||
chr3:179778623 | G | A | 3 | a0001c0001t0014g0184 a0001c0001t0014g0276 a0001c0001t0023g0262 |
3 | HG03130.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2414-3116G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778623 | |||||||
chr3:179778647 | T | C | 1 | a0001c0003t0001g0230 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2414-3092T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778647 | |||||||
chr3:179778677 | A | C | 46 | a0001c0001t0004g0018 a0001c0001t0004g0105 a0001c0001t0004g0206 others(43): Show |
46 | HG00140.hp2 HG01081.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.2414-3062A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778677 | |||||||
chr3:179778706 | C | G | 4 | a0001c0001t0001g0260 a0001c0002t0001g0139 a0001c0002t0001g0177 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2414-3033C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778706 | |||||||
chr3:179778789 | G | A | 1 | a0001c0006t0032g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2414-2950G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179778789 | |||||||
chr3:179778984 | AAG | A | 64 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(61): Show |
65 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2414-2750_2414-274 others(6): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179778984 | ||||||
chr3:179779055 | G | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0222 a0001c0001t0001g0274 others(1): Show |
4 | HG00642.hp1 HG01257.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.2414-2684G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779055 | |||||||
chr3:179779080 | G | A | 1 | a0001c0001t0022g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2414-2659G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779080 | |||||||
chr3:179779086 | C | G | 1 | a0001c0001t0026g0049 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2414-2653C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779086 | |||||||
chr3:179779094 | C | G | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2414-2645C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779094 | |||||||
chr3:179779139 | A | C | 3 | a0001c0001t0008g0040 a0001c0002t0008g0164 a0001c0002t0008g0165 |
3 | HG01070.hp1 HG01071.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2414-2600A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779139 | |||||||
chr3:179779185 | A | G | 2 | a0001c0001t0001g0050 a0001c0002t0001g0146 |
2 | NA18947.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.2414-2554A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779185 | |||||||
chr3:179779232 | TA | T | 46 | a0001c0001t0004g0018 a0001c0001t0004g0105 a0001c0001t0004g0206 others(43): Show |
46 | HG00140.hp2 HG01081.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.2414-2496delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179779232 | ||||||
chr3:179779456 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2414-2283G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779456 | |||||||
chr3:179779458 | G | A | 71 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(68): Show |
71 | HG00140.hp2 HG01081.hp2 HG01099.hp1 others(68): Show |
intron_variant | MODIFIER | c.2414-2281G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779458 | |||||||
chr3:179779478 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2414-2261C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779478 | |||||||
chr3:179779707 | G | A | 1 | a0001c0005t0005g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2414-2032G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779707 | |||||||
chr3:179779712 | G | C | 1 | a0001c0001t0001g0041 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2414-2027G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779712 | |||||||
chr3:179779719 | TA | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(79): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.2414-2002delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179779719 | ||||||
chr3:179779734 | A | G | 18 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0004g0105 others(15): Show |
18 | HG01928.hp1 HG01978.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2414-2005A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179779734 | |||||||
chr3:179780282 | A | G | 1 | a0001c0012t0004g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2414-1457A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780282 | |||||||
chr3:179780400 | A | G | 3 | a0001c0001t0008g0040 a0001c0002t0008g0164 a0001c0002t0008g0165 |
3 | HG01070.hp1 HG01071.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2414-1339A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780400 | |||||||
chr3:179780406 | C | T | 9 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2414-1333C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780406 | |||||||
chr3:179780515 | A | G | 146 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(143): Show |
146 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.2414-1224A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780515 | |||||||
chr3:179780535 | G | T | 1 | a0001c0001t0002g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2414-1204G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780535 | |||||||
chr3:179780583 | G | A | 1 | a0001c0001t0022g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2414-1156G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780583 | |||||||
chr3:179780723 | T | G | 8 | a0001c0001t0008g0040 a0001c0001t0008g0198 a0001c0001t0008g0293 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2414-1016T>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780723 | |||||||
chr3:179780795 | A | G | 1 | a0001c0016t0004g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2414-944A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780795 | |||||||
chr3:179780897 | C | T | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2414-842C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780897 | |||||||
chr3:179780917 | AT | A | 25 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(22): Show |
25 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2414-819delT | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 179780917 | ||||||
chr3:179780934 | G | A | 8 | a0001c0001t0008g0040 a0001c0001t0008g0198 a0001c0001t0008g0293 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2414-805G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780934 | |||||||
chr3:179780981 | C | T | 1 | a0001c0001t0002g0005 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2414-758C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179780981 | |||||||
chr3:179781102 | A | C | 1 | a0001c0001t0019g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2414-637A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179781102 | |||||||
chr3:179781177 | C | A | 75 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(72): Show |
75 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.2414-562C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179781177 | |||||||
chr3:179781217 | G | A | 20 | a0001c0001t0004g0018 a0001c0001t0004g0206 a0001c0001t0004g0234 others(17): Show |
20 | HG01081.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2414-522G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179781217 | |||||||
chr3:179781399 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2414-340C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179781399 | |||||||
chr3:179781427 | G | T | 14 | a0001c0001t0006g0035 a0001c0001t0006g0073 a0001c0001t0006g0081 others(11): Show |
14 | HG00140.hp2 HG00741.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2414-312G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179781427 | |||||||
chr3:179781492 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2414-247C>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179781492 | |||||||
chr3:179781543 | T | TG | 150 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(147): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.2414-196_2414-195i others(3): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 19/20 | chr3 | 179781543 | |||||||
chr3:179782097 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2498+274C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179782097 | |||||||
chr3:179782172 | G | A | 75 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(72): Show |
75 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.2498+349G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179782172 | |||||||
chr3:179782440 | G | A | 2 | a0001c0001t0017g0192 a0001c0006t0032g0140 |
2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2498+617G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179782440 | |||||||
chr3:179782524 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2498+701G>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179782524 | |||||||
chr3:179782531 | C | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0020g0059 |
3 | HG02080.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.2498+708C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179782531 | |||||||
chr3:179782575 | G | A | 1 | a0001c0001t0004g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2498+752G>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179782575 | |||||||
chr3:179782763 | G | C | 1 | a0001c0001t0002g0005 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2498+940G>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179782763 | |||||||
chr3:179782837 | C | A | 1 | a0001c0002t0043g0125 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2498+1014C>A | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179782837 | |||||||
chr3:179783034 | C | T | 15 | a0001c0001t0001g0027 a0001c0001t0006g0035 a0001c0001t0006g0073 others(12): Show |
15 | HG00140.hp2 HG00741.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2499-1014C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179783034 | |||||||
chr3:179783113 | A | C | 50 | a0001c0001t0004g0018 a0001c0001t0004g0105 a0001c0001t0004g0206 others(47): Show |
50 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.2499-935A>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179783113 | |||||||
chr3:179783186 | A | G | 9 | a0001c0001t0001g0030 a0001c0001t0001g0052 a0001c0001t0001g0110 others(6): Show |
9 | HG00558.hp2 HG00673.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.2499-862A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179783186 | |||||||
chr3:179783352 | AAC | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG00673.hp1 HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2499-691_2499-690d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr3 | 179783352 | ||||||
chr3:179783579 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2499-469A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179783579 | |||||||
chr3:179783621 | A | G | 1 | a0001c0001t0030g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2499-427A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179783621 | |||||||
chr3:179783815 | T | C | 16 | a0001c0001t0005g0017 a0001c0001t0005g0202 a0001c0001t0005g0231 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2499-233T>C | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179783815 | |||||||
chr3:179783860 | TA | T | 17 | a0001c0001t0001g0211 a0001c0001t0001g0218 a0001c0001t0001g0274 others(14): Show |
17 | HG00140.hp2 HG00597.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.2499-171delA | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr3 | 179783860 | ||||||
chr3:179783860 | TAA | T | 65 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0022 others(62): Show |
65 | HG01081.hp2 HG01109.hp1 HG01255.hp1 others(62): Show |
intron_variant | MODIFIER | c.2499-172_2499-171d others(4): Show |
USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr3 | 179783860 | ||||||
chr3:179783876 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2499-172A>G | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179783876 | |||||||
chr3:179783918 | C | T | 1 | a0001c0001t0003g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2499-130C>T | USP13 | ENSG00000058056.10 | transcript | ENST00000263966.8 | protein_coding | 20/20 | chr3 | 179783918 |