Item | Value |
---|---|
geneid | 131405 |
ensemblid | ENSG00000206557.6 |
hgncid | 32669 |
symbol | TRIM71 |
name | tripartite motif containing 71 |
refseq_nuc | NM_001039111.3 |
refseq_prot | NP_001034200.1 |
ensembl_nuc | ENST00000383763.6 |
ensembl_prot | ENSP00000373272.3 |
mane_status | MANE Select |
chr | chr3 |
start | 32817997 |
end | 32897824 |
strand | + |
ver | v1.2 |
region | chr3:32817997-32897824 |
region5000 | chr3:32812997-32902824 |
regionname0 | TRIM71_chr3_32817997_32897824 |
regionname5000 | TRIM71_chr3_32812997_32902824 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 868 | 325 | 92 | 50 | 131 | 16 | 34 | 95 | TRIM71_chr3_32812997_32902824 | TRIM71 | MASFP others(863): Show |
chr3 | 32812997 | 32902824 |
a0002 | 0/0 | 868 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | MASFP others(863): Show |
chr3 | 32812997 | 32902824 |
a0003 | 0/0 | 868 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | MASFP others(863): Show |
chr3 | 32812997 | 32902824 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2604 | 234 | 62 | 38 | 89 | 15 | 29 | TRIM71_chr3_32812997_32902824 | TRIM71 | ATGGC others(2599): Show |
chr3 | 32812997 | 32902824 | ||
a0001c0002 | 0/0 | 2604 | 69 | 11 | 11 | 42 | 0 | 5 | TRIM71_chr3_32812997_32902824 | TRIM71 | ATGGC others(2599): Show |
chr3 | 32812997 | 32902824 | ||
a0001c0003 | 0/0 | 2604 | 16 | 15 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ATGGC others(2599): Show |
chr3 | 32812997 | 32902824 | ||
a0001c0004 | 1/0 | 2604 | 4 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ATGGC others(2599): Show |
chr3 | 32812997 | 32902824 | ||
a0001c0007 | 0/0 | 2604 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ATGGC others(2599): Show |
chr3 | 32812997 | 32902824 | ||
a0001c0008 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ATGGC others(2599): Show |
chr3 | 32812997 | 32902824 | ||
a0002c0005 | 0/0 | 2604 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ATGGC others(2599): Show |
chr3 | 32812997 | 32902824 | ||
a0003c0006 | 0/0 | 2604 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ATGGC others(2599): Show |
chr3 | 32812997 | 32902824 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8706 | 72 | 10 | 16 | 23 | 7 | 16 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0002 | 0/0 | 8704 | 17 | 16 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0003 | 0/1 | 8699 | 23 | 4 | 8 | 3 | 3 | 4 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8694): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0004 | 0/0 | 8702 | 17 | 0 | 0 | 16 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8697): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0006 | 0/0 | 8706 | 13 | 0 | 0 | 13 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0007 | 0/0 | 8704 | 10 | 9 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0008 | 0/0 | 8702 | 11 | 0 | 0 | 11 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8697): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0009 | 0/0 | 8704 | 8 | 1 | 3 | 0 | 2 | 2 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0010 | 0/0 | 8708 | 4 | 2 | 2 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8703): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0012 | 0/0 | 8699 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8694): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0014 | 0/0 | 8708 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8703): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0015 | 0/0 | 8706 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0016 | 0/0 | 8704 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0017 | 0/0 | 8706 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0018 | 0/0 | 8708 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8703): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0019 | 0/0 | 8707 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8702): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0020 | 0/0 | 8702 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8697): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0021 | 0/0 | 8706 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0022 | 0/0 | 8706 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0026 | 0/0 | 8699 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8694): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0027 | 0/0 | 8706 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0028 | 0/0 | 8708 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8703): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0029 | 0/0 | 8699 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8694): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0030 | 0/0 | 8706 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0031 | 0/0 | 8706 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0032 | 0/0 | 8706 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0033 | 0/0 | 8707 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8702): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0034 | 0/0 | 8706 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0035 | 0/0 | 8706 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0036 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0037 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0038 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0039 | 0/0 | 8707 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8702): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0040 | 0/0 | 8706 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0041 | 0/0 | 8702 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8697): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0042 | 0/0 | 8706 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0043 | 0/0 | 8706 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0044 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0045 | 0/0 | 8704 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0048 | 0/0 | 8699 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8694): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0049 | 0/0 | 8699 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8694): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0050 | 0/0 | 8699 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8694): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0051 | 0/0 | 8704 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0052 | 0/0 | 8700 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8695): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0053 | 0/0 | 8707 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8702): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0054 | 0/0 | 8706 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0055 | 0/0 | 8702 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8697): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0056 | 0/0 | 8702 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8697): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0057 | 0/0 | 8703 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8698): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0058 | 0/0 | 8700 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8695): Show |
chr3 | 32812997 | 32902824 |
a0001c0001t0059 | 0/0 | 8706 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0002t0001 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0001c0002t0002 | 0/0 | 8704 | 56 | 10 | 8 | 34 | 0 | 4 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0002t0013 | 0/0 | 8704 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0002t0023 | 0/0 | 8704 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0002t0024 | 0/0 | 8704 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0002t0025 | 0/0 | 8702 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8697): Show |
chr3 | 32812997 | 32902824 |
a0001c0002t0046 | 0/0 | 8704 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0002t0047 | 0/0 | 8704 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0003t0005 | 0/0 | 8704 | 16 | 15 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0004t0011 | 1/0 | 8704 | 4 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0001c0007t0012 | 0/0 | 8699 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8694): Show |
chr3 | 32812997 | 32902824 |
a0001c0008t0007 | 0/0 | 8704 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
a0002c0005t0001 | 0/0 | 8706 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8701): Show |
chr3 | 32812997 | 32902824 |
a0003c0006t0002 | 0/0 | 8704 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | ACTCC others(8699): Show |
chr3 | 32812997 | 32902824 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0007g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0007g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0007g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0008g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0009g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0009g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0009g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0009g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0010g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0010g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0010g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0012g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0012g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0014g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0014g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0014g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0015g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0015g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0015g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0016g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0016g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0017g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0017g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0017g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0018g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0018g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0019g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0019g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0020g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0020g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0021g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0021g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0022g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0022g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0026g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0026g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0027g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0027g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0028g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0029g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0030g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0031g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0032g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0033g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0034g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0035g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0036g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0037g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0038g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0039g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0040g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0041g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0042g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0043g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0044g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0045g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0048g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0049g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0050g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0051g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0052g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0053g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0054g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0055g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0056g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0057g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0058g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0001t0059g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0013g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0013g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0013g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0013g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0023g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0023g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0024g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0024g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0025g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0025g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0046g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0002t0047g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0003t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0004t0011g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0004t0011g0304 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0004t0011g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0004t0011g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0007t0012g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0001c0008t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0002c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0002c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
a0003c0006t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0191 | EUR | GBR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00140 | hp1 | a0001 | c0001 | t0009 | g0154 | EUR | GBR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00140 | hp2 | a0001 | c0001 | t0034 | g0252 | EUR | GBR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | FIN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0216 | EUR | FIN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00323 | hp1 | a0001 | c0007 | t0012 | g0133 | EUR | FIN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00323 | hp2 | a0001 | c0001 | t0028 | g0220 | EUR | FIN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00438 | hp1 | a0002 | c0005 | t0001 | g0159 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00544 | hp1 | a0001 | c0002 | t0025 | g0209 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00544 | hp2 | a0001 | c0001 | t0027 | g0277 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00621 | hp1 | a0002 | c0005 | t0001 | g0008 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0069 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0134 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0226 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0111 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01167 | hp1 | a0001 | c0001 | t0009 | g0240 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01167 | hp2 | a0001 | c0001 | t0012 | g0169 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01175 | hp2 | a0001 | c0001 | t0014 | g0280 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0253 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0153 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0235 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01243 | hp2 | a0001 | c0001 | t0030 | g0323 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01255 | hp1 | a0001 | c0001 | t0059 | g0127 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01255 | hp2 | a0001 | c0001 | t0010 | g0236 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01256 | hp2 | a0001 | c0001 | t0014 | g0246 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01258 | hp1 | a0001 | c0001 | t0014 | g0250 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01258 | hp2 | a0001 | c0001 | t0031 | g0150 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01358 | hp2 | a0001 | c0002 | t0024 | g0137 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0192 | EUR | IBS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01517 | hp1 | a0001 | c0001 | t0009 | g0148 | EUR | IBS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01884 | hp1 | a0001 | c0004 | t0011 | g0309 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01884 | hp2 | a0001 | c0008 | t0007 | g0025 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01891 | hp1 | a0001 | c0001 | t0010 | g0237 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01891 | hp2 | a0001 | c0003 | t0005 | g0298 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01934 | hp2 | a0001 | c0003 | t0005 | g0027 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0092 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01952 | hp2 | a0001 | c0002 | t0024 | g0206 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01978 | hp1 | a0001 | c0002 | t0046 | g0065 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02015 | hp1 | a0001 | c0001 | t0006 | g0167 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02015 | hp2 | a0001 | c0001 | t0021 | g0047 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02056 | hp1 | a0001 | c0001 | t0033 | g0179 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02056 | hp2 | a0001 | c0001 | t0019 | g0324 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02074 | hp2 | a0001 | c0001 | t0008 | g0266 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02080 | hp2 | a0001 | c0001 | t0008 | g0274 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02132 | hp1 | a0001 | c0001 | t0008 | g0275 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02132 | hp2 | a0001 | c0001 | t0006 | g0132 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | CDX | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02155 | hp2 | a0001 | c0002 | t0013 | g0256 | EAS | CDX | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | CDX | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02165 | hp2 | a0001 | c0001 | t0021 | g0174 | EAS | CDX | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0312 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02258 | hp2 | a0001 | c0001 | t0015 | g0072 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0121 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02523 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02523 | hp2 | a0001 | c0001 | t0006 | g0031 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02572 | hp1 | a0001 | c0003 | t0005 | g0024 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02615 | hp1 | a0001 | c0001 | t0012 | g0063 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0308 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02622 | hp1 | a0001 | c0003 | t0005 | g0297 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02630 | hp1 | a0001 | c0003 | t0005 | g0117 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02647 | hp1 | a0001 | c0003 | t0005 | g0282 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02647 | hp2 | a0001 | c0001 | t0045 | g0071 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02683 | hp2 | a0001 | c0002 | t0047 | g0101 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0186 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02717 | hp2 | a0001 | c0003 | t0005 | g0321 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02723 | hp1 | a0001 | c0001 | t0026 | g0319 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02735 | hp1 | a0001 | c0001 | t0017 | g0278 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02735 | hp2 | a0001 | c0001 | t0009 | g0115 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02809 | hp1 | a0001 | c0003 | t0005 | g0068 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02809 | hp2 | a0001 | c0003 | t0005 | g0300 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0310 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02818 | hp2 | a0001 | c0001 | t0037 | g0320 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0322 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02896 | hp2 | a0001 | c0003 | t0005 | g0283 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02965 | hp1 | a0001 | c0003 | t0005 | g0084 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02965 | hp2 | a0001 | c0001 | t0016 | g0079 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0119 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02976 | hp2 | a0001 | c0001 | t0036 | g0301 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03041 | hp2 | a0001 | c0001 | t0038 | g0316 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03130 | hp2 | a0001 | c0004 | t0011 | g0243 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03139 | hp1 | a0001 | c0001 | t0016 | g0003 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03195 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03209 | hp2 | a0001 | c0001 | t0026 | g0066 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0098 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03239 | hp2 | a0001 | c0001 | t0009 | g0090 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0242 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03491 | hp2 | a0001 | c0001 | t0042 | g0107 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03492 | hp2 | a0001 | c0001 | t0049 | g0128 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03540 | hp2 | a0001 | c0003 | t0005 | g0120 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03579 | hp1 | a0001 | c0003 | t0005 | g0311 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03579 | hp2 | a0001 | c0001 | t0016 | g0003 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03669 | hp2 | a0001 | c0001 | t0035 | g0081 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03688 | hp2 | a0001 | c0001 | t0050 | g0095 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0058 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03834 | hp1 | a0001 | c0001 | t0040 | g0254 | SAS | BEB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | BEB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | BEB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG04228 | hp1 | a0001 | c0001 | t0027 | g0259 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | CHB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18906 | hp1 | a0001 | c0001 | t0018 | g0281 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18906 | hp2 | a0001 | c0003 | t0005 | g0299 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18945 | hp1 | a0001 | c0001 | t0041 | g0034 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18947 | hp1 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18947 | hp2 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18962 | hp1 | a0001 | c0001 | t0017 | g0257 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18962 | hp2 | a0001 | c0002 | t0025 | g0147 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18963 | hp1 | a0003 | c0006 | t0002 | g0193 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18964 | hp2 | a0001 | c0001 | t0008 | g0271 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18966 | hp1 | a0001 | c0001 | t0022 | g0156 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18966 | hp2 | a0001 | c0001 | t0020 | g0049 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18968 | hp1 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18973 | hp2 | a0001 | c0002 | t0013 | g0265 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18977 | hp2 | a0001 | c0001 | t0008 | g0263 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18978 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18979 | hp1 | a0001 | c0001 | t0019 | g0195 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18981 | hp1 | a0001 | c0002 | t0023 | g0053 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18983 | hp1 | a0001 | c0001 | t0043 | g0182 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18990 | hp1 | a0001 | c0001 | t0056 | g0272 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18990 | hp2 | a0001 | c0001 | t0006 | g0130 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18992 | hp2 | a0001 | c0001 | t0020 | g0041 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA18998 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19003 | hp1 | a0001 | c0001 | t0055 | g0268 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19004 | hp1 | a0001 | c0002 | t0023 | g0046 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19005 | hp2 | a0001 | c0002 | t0013 | g0264 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19007 | hp1 | a0001 | c0001 | t0006 | g0286 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0043 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19009 | hp2 | a0001 | c0001 | t0017 | g0258 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19012 | hp2 | a0001 | c0001 | t0053 | g0269 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19043 | hp1 | a0001 | c0004 | t0011 | g0305 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19043 | hp2 | a0001 | c0001 | t0044 | g0080 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19056 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19056 | hp2 | a0001 | c0001 | t0008 | g0273 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19060 | hp2 | a0001 | c0001 | t0029 | g0255 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19065 | hp1 | a0001 | c0002 | t0013 | g0267 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19065 | hp2 | a0001 | c0001 | t0032 | g0044 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19068 | hp1 | a0001 | c0001 | t0008 | g0276 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19074 | hp2 | a0001 | c0001 | t0008 | g0227 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19077 | hp1 | a0001 | c0001 | t0058 | g0223 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19077 | hp2 | a0001 | c0001 | t0006 | g0228 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19078 | hp2 | a0001 | c0001 | t0057 | g0270 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19082 | hp2 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19083 | hp2 | a0001 | c0001 | t0052 | g0104 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19087 | hp1 | a0001 | c0001 | t0054 | g0279 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19091 | hp1 | a0001 | c0001 | t0022 | g0165 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0070 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ASW | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0185 | AFR | ASW | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0188 | EUR | TSI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | GIH | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | GIH | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG01123 | hp2 | a0001 | c0001 | t0009 | g0224 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02109 | hp2 | a0001 | c0001 | t0048 | g0152 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02559 | hp1 | a0001 | c0003 | t0005 | g0097 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG02559 | hp2 | a0001 | c0001 | t0018 | g0099 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG06807 | hp1 | a0001 | c0001 | t0015 | g0244 | AFR | USA | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
HG06807 | hp2 | a0001 | c0001 | t0039 | g0026 | AFR | USA | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20300 | hp1 | a0001 | c0001 | t0051 | g0096 | AFR | USA | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | USA | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA21309 | hp1 | a0001 | c0003 | t0005 | g0285 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
NA21309 | hp2 | a0001 | c0001 | t0015 | g0073 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0144 | REF | REF | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
homoSapiens | grch38p0 | a0001 | c0004 | t0011 | g0304 | REF | REF | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:32818133 | T | G | 1 | a0003 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.53T>G | p.Met18Arg | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/4 | 137/8704 | 53/2607 | 18/868 | chr3 | 32818133 | |||
chr3:32890543 | G | A | 1 | a0002 | 2 | HG00438.hp1 HG00621.hp1 |
missense_variant | MODERATE | c.1339G>A | p.Val447Met | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1423/8704 | 1339/2607 | 447/868 | chr3 | 32890543 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:32818383 | C | G | 1 | a0001c0008 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.303C>G | p.Ala101Ala | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/4 | 387/8704 | 303/2607 | 101/868 | chr3 | 32818383 | |||
chr3:32886017 | G | T | 7 | a0001c0001 a0001c0002 a0001c0003 others(4): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
synonymous_variant | LOW | c.1104G>T | p.Thr368Thr | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/4 | 1188/8704 | 1104/2607 | 368/868 | chr3 | 32886017 | |||
chr3:32891163 | C | T | 1 | a0001c0007 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.1959C>T | p.Phe653Phe | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2043/8704 | 1959/2607 | 653/868 | chr3 | 32891163 | |||
chr3:32891544 | G | A | 2 | a0001c0002 a0003c0006 |
70 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(67): Show |
synonymous_variant | LOW | c.2340G>A | p.Ser780Ser | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2424/8704 | 2340/2607 | 780/868 | chr3 | 32891544 | |||
chr3:32891637 | G | A | 1 | a0001c0003 | 16 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(13): Show |
synonymous_variant | LOW | c.2433G>A | p.Ala811Ala | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2517/8704 | 2433/2607 | 811/868 | chr3 | 32891637 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:32818002 | C | T | 1 | a0001c0001t0059 | 1 | HG01255.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/4 | 79 | chr3 | 32818002 | ||||||
chr3:32818028 | C | T | 10 | a0001c0001t0008 a0001c0001t0017 a0001c0001t0027 others(7): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-53C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/4 | 53 | chr3 | 32818028 | ||||||
chr3:32891852 | G | GTC | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(31): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*61_*62dupCT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 63 | INFO_REALIGN_3_PRIME | chr3 | 32891852 | |||||
chr3:32891852 | G | GTCTC | 4 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(1): Show |
10 | HG00323.hp2 HG01175.hp2 HG01243.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*59_*62dupCTCT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 63 | INFO_REALIGN_3_PRIME | chr3 | 32891852 | |||||
chr3:32891870 | C | T | 10 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(7): Show |
41 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*59C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 59 | chr3 | 32891870 | ||||||
chr3:32891874 | T | C | 11 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(8): Show |
42 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*63T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 63 | chr3 | 32891874 | ||||||
chr3:32891876 | C | T | 11 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(8): Show |
42 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*65C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 65 | chr3 | 32891876 | ||||||
chr3:32891880 | T | C | 11 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(8): Show |
42 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*69T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 69 | chr3 | 32891880 | ||||||
chr3:32891890 | T | C | 1 | a0001c0001t0048 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*79T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 79 | chr3 | 32891890 | ||||||
chr3:32892016 | A | G | 1 | a0001c0001t0022 | 2 | NA18966.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*205A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 205 | chr3 | 32892016 | ||||||
chr3:32892318 | G | A | 1 | a0001c0001t0049 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 507 | chr3 | 32892318 | ||||||
chr3:32892719 | A | G | 1 | a0001c0001t0044 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*908A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 908 | chr3 | 32892719 | ||||||
chr3:32892999 | T | G | 1 | a0001c0003t0005 | 16 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1188T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1188 | chr3 | 32892999 | ||||||
chr3:32893011 | A | G | 1 | a0001c0001t0043 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1200A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1200 | chr3 | 32893011 | ||||||
chr3:32893251 | G | A | 1 | a0001c0002t0023 | 2 | NA18981.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1440G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1440 | chr3 | 32893251 | ||||||
chr3:32893265 | A | G | 1 | a0001c0001t0016 | 3 | HG02965.hp2 HG03139.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1454A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1454 | chr3 | 32893265 | ||||||
chr3:32893290 | C | T | 1 | a0001c0001t0021 | 2 | HG02015.hp2 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1479C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1479 | chr3 | 32893290 | ||||||
chr3:32893634 | A | G | 12 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(9): Show |
43 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1823A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1823 | chr3 | 32893634 | ||||||
chr3:32893663 | C | G | 2 | a0001c0001t0009 a0001c0001t0042 |
9 | HG00140.hp1 HG01069.hp1 HG01123.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1852C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1852 | chr3 | 32893663 | ||||||
chr3:32893719 | T | C | 1 | a0001c0001t0016 | 3 | HG02965.hp2 HG03139.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1908T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1908 | chr3 | 32893719 | ||||||
chr3:32893759 | C | T | 3 | a0001c0001t0007 a0001c0002t0047 a0001c0008t0007 |
12 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1948C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1948 | chr3 | 32893759 | ||||||
chr3:32893765 | CCT | C | 8 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0020 others(5): Show |
35 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1957_*1958delCT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1957 | INFO_REALIGN_3_PRIME | chr3 | 32893765 | |||||
chr3:32894023 | T | C | 14 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(11): Show |
45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2212T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2212 | chr3 | 32894023 | ||||||
chr3:32894134 | T | G | 1 | a0001c0002t0024 | 2 | HG01358.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2323T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2323 | chr3 | 32894134 | ||||||
chr3:32894327 | A | G | 13 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(10): Show |
44 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2516A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2516 | chr3 | 32894327 | ||||||
chr3:32894412 | C | T | 1 | a0001c0003t0005 | 16 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2601C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2601 | chr3 | 32894412 | ||||||
chr3:32894750 | G | A | 1 | a0001c0001t0032 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2939G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2939 | chr3 | 32894750 | ||||||
chr3:32894863 | G | T | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*3052G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3052 | chr3 | 32894863 | ||||||
chr3:32894937 | T | C | 2 | a0001c0001t0048 a0001c0001t0050 |
2 | HG02109.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3126T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3126 | chr3 | 32894937 | ||||||
chr3:32895079 | C | G | 2 | a0001c0001t0007 a0001c0008t0007 |
11 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3268C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3268 | chr3 | 32895079 | ||||||
chr3:32895080 | T | C | 6 | a0001c0001t0006 a0001c0001t0027 a0001c0001t0028 others(3): Show |
19 | HG00323.hp2 HG00544.hp2 HG02015.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3269T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3269 | chr3 | 32895080 | ||||||
chr3:32895313 | G | A | 1 | a0001c0001t0054 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3502G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3502 | chr3 | 32895313 | ||||||
chr3:32895511 | T | G | 1 | a0001c0001t0034 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3700T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3700 | chr3 | 32895511 | ||||||
chr3:32895516 | C | A | 22 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(19): Show |
99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*3705C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3705 | chr3 | 32895516 | ||||||
chr3:32895549 | T | C | 1 | a0001c0002t0023 | 2 | NA18981.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3738T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3738 | chr3 | 32895549 | ||||||
chr3:32895632 | A | G | 1 | a0001c0001t0040 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3821A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3821 | chr3 | 32895632 | ||||||
chr3:32895694 | G | C | 1 | a0001c0001t0015 | 3 | HG02258.hp2 HG06807.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3883G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3883 | chr3 | 32895694 | ||||||
chr3:32895717 | A | C | 2 | a0001c0001t0012 a0001c0007t0012 |
4 | HG00323.hp1 HG01167.hp2 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3906A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3906 | chr3 | 32895717 | ||||||
chr3:32896104 | C | T | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(33): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*4293C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4293 | chr3 | 32896104 | ||||||
chr3:32896162 | C | G | 1 | a0001c0001t0026 | 2 | HG02723.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4351C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4351 | chr3 | 32896162 | ||||||
chr3:32896183 | T | G | 8 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0020 others(5): Show |
35 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4372T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4372 | chr3 | 32896183 | ||||||
chr3:32896232 | A | C | 1 | a0001c0002t0046 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4421A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4421 | chr3 | 32896232 | ||||||
chr3:32896240 | G | A | 1 | a0001c0001t0035 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4429G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4429 | chr3 | 32896240 | ||||||
chr3:32896442 | G | GT | 6 | a0001c0001t0019 a0001c0001t0033 a0001c0001t0039 others(3): Show |
7 | HG02056.hp1 HG02056.hp2 HG06807.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4641dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4642 | INFO_REALIGN_3_PRIME | chr3 | 32896442 | |||||
chr3:32896632 | T | C | 1 | a0001c0001t0036 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4821T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4821 | chr3 | 32896632 | ||||||
chr3:32896957 | T | C | 4 | a0001c0001t0020 a0001c0001t0055 a0001c0001t0058 others(1): Show |
6 | HG00544.hp1 NA18962.hp2 NA18966.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5146T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5146 | chr3 | 32896957 | ||||||
chr3:32896976 | ATTCCT | A | 9 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0026 others(6): Show |
33 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5169_*5173delCTTT others(1): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5169 | INFO_REALIGN_3_PRIME | chr3 | 32896976 | |||||
chr3:32897010 | G | A | 2 | a0001c0001t0037 a0001c0001t0039 |
2 | HG02818.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5199G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5199 | chr3 | 32897010 | ||||||
chr3:32897017 | G | A | 2 | a0001c0001t0038 a0001c0001t0045 |
2 | HG02647.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5206G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5206 | chr3 | 32897017 | ||||||
chr3:32897040 | G | A | 1 | a0001c0001t0056 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5229G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5229 | chr3 | 32897040 | ||||||
chr3:32897370 | G | C | 1 | a0001c0001t0016 | 3 | HG02965.hp2 HG03139.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5559G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5559 | chr3 | 32897370 | ||||||
chr3:32897515 | T | G | 1 | a0001c0001t0041 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5704T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5704 | chr3 | 32897515 | ||||||
chr3:32897521 | TCC | T | 9 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0020 others(6): Show |
37 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5715_*5716delCC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5715 | INFO_REALIGN_3_PRIME | chr3 | 32897521 | |||||
chr3:32897561 | T | C | 1 | a0001c0001t0018 | 2 | HG02559.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5750T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5750 | chr3 | 32897561 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:32819052 | C | T | 1 | a0001c0001t0019g0324 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.852+120C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819052 | |||||||
chr3:32819189 | C | G | 1 | a0001c0001t0030g0323 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.852+257C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819189 | |||||||
chr3:32819206 | G | T | 7 | a0001c0001t0002g0317 a0001c0001t0002g0318 a0001c0001t0026g0319 others(4): Show |
7 | HG02717.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+274G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819206 | |||||||
chr3:32819237 | G | A | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.852+305G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819237 | |||||||
chr3:32819268 | GCCTGCT | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.852+344_852+349del others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32819268 | ||||||
chr3:32819309 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.852+377G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819309 | |||||||
chr3:32819479 | G | T | 3 | a0001c0001t0001g0302 a0001c0001t0016g0003 a0001c0001t0036g0301 |
4 | HG02896.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+547G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819479 | |||||||
chr3:32819522 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0002c0005t0001g0008 |
3 | HG00423.hp1 HG00621.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.852+590T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819522 | |||||||
chr3:32819610 | A | G | 4 | a0001c0003t0005g0297 a0001c0003t0005g0298 a0001c0003t0005g0299 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.852+678A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819610 | |||||||
chr3:32819634 | C | G | 1 | a0001c0001t0002g0296 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.852+702C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819634 | |||||||
chr3:32819704 | A | G | 9 | a0001c0001t0004g0294 a0001c0002t0002g0287 a0001c0002t0002g0288 others(6): Show |
9 | HG02027.hp1 NA18945.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.852+772A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819704 | |||||||
chr3:32819968 | C | T | 1 | a0001c0001t0006g0286 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.852+1036C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819968 | |||||||
chr3:32820025 | T | G | 1 | a0001c0001t0001g0009 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.852+1093T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820025 | |||||||
chr3:32820026 | G | A | 1 | a0001c0001t0012g0010 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.852+1094G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820026 | |||||||
chr3:32820046 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.852+1114G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820046 | |||||||
chr3:32820064 | G | T | 2 | a0001c0001t0007g0284 a0001c0003t0005g0285 |
2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+1132G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820064 | |||||||
chr3:32820069 | G | A | 1 | a0001c0001t0036g0301 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.852+1137G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820069 | |||||||
chr3:32820136 | A | G | 58 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(55): Show |
58 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.852+1204A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820136 | |||||||
chr3:32820143 | G | A | 1 | a0001c0001t0006g0012 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.852+1211G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820143 | |||||||
chr3:32820293 | C | T | 2 | a0001c0003t0005g0282 a0001c0003t0005g0283 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.852+1361C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820293 | |||||||
chr3:32820828 | A | G | 3 | a0001c0001t0003g0225 a0001c0001t0009g0224 a0001c0001t0009g0226 |
3 | HG01069.hp1 HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.852+1896A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820828 | |||||||
chr3:32821043 | G | C | 1 | a0001c0001t0001g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+2111G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821043 | |||||||
chr3:32821449 | A | C | 3 | a0001c0001t0007g0284 a0001c0003t0005g0285 a0001c0003t0005g0300 |
3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+2517A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821449 | |||||||
chr3:32821474 | TA | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(55): Show |
58 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.852+2546delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32821474 | ||||||
chr3:32821480 | G | T | 3 | a0001c0003t0005g0297 a0001c0003t0005g0298 a0001c0003t0005g0299 |
3 | HG01891.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+2548G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821480 | |||||||
chr3:32821575 | A | G | 1 | a0001c0002t0002g0322 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.852+2643A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821575 | |||||||
chr3:32821585 | G | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.852+2653G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821585 | |||||||
chr3:32821789 | A | C | 1 | a0001c0002t0002g0122 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.852+2857A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821789 | |||||||
chr3:32821789 | A | T | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.852+2857A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821789 | |||||||
chr3:32821998 | T | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0002t0002g0124 |
3 | NA18948.hp1 NA18969.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.852+3066T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821998 | |||||||
chr3:32822082 | C | A | 1 | a0001c0001t0001g0009 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.852+3150C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822082 | |||||||
chr3:32822515 | C | A | 1 | a0001c0001t0008g0227 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.852+3583C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822515 | |||||||
chr3:32822549 | T | C | 1 | a0001c0002t0002g0322 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.852+3617T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822549 | |||||||
chr3:32822579 | C | A | 11 | a0001c0001t0001g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(8): Show |
11 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.852+3647C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822579 | |||||||
chr3:32822584 | G | A | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0006g0228 |
3 | HG02040.hp1 HG02129.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.852+3652G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822584 | |||||||
chr3:32822634 | C | T | 3 | a0001c0001t0007g0119 a0001c0001t0007g0121 a0001c0003t0005g0120 |
3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.852+3702C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822634 | |||||||
chr3:32822652 | A | AT | 69 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0229 others(66): Show |
69 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.852+3724dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32822652 | ||||||
chr3:32822939 | A | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+4007A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822939 | |||||||
chr3:32822946 | A | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(69): Show |
74 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.852+4014A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822946 | |||||||
chr3:32822958 | G | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(61): Show |
64 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.852+4026G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822958 | |||||||
chr3:32822979 | A | G | 1 | a0001c0001t0018g0281 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.852+4047A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822979 | |||||||
chr3:32823015 | T | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0229 others(62): Show |
65 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.852+4083T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823015 | |||||||
chr3:32823049 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(69): Show |
74 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.852+4117C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823049 | |||||||
chr3:32823198 | G | T | 1 | a0001c0001t0014g0280 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.852+4266G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823198 | |||||||
chr3:32823273 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.852+4341G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823273 | |||||||
chr3:32823624 | T | C | 1 | a0001c0001t0059g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.852+4692T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823624 | |||||||
chr3:32823690 | T | TTGCAGTG others(41): Show |
2 | a0001c0001t0001g0014 a0001c0003t0005g0024 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+4773_852+4774i others(50): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32823690 | ||||||
chr3:32823708 | G | A | 2 | a0001c0001t0001g0014 a0001c0003t0005g0024 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+4776G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823708 | |||||||
chr3:32823708 | G | GCAGTGAG others(25): Show |
1 | a0001c0002t0013g0256 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.852+4788_852+4789i others(34): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32823708 | ||||||
chr3:32823708 | G | GCAGTGAG others(41): Show |
25 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(22): Show |
25 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.852+4788_852+4789i others(50): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32823708 | ||||||
chr3:32823850 | G | C | 1 | a0001c0001t0049g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.852+4918G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823850 | |||||||
chr3:32823946 | G | A | 1 | a0001c0002t0002g0129 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.852+5014G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823946 | |||||||
chr3:32824041 | C | T | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+5109C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824041 | |||||||
chr3:32824056 | C | CAG | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.852+5125_852+5126d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32824056 | ||||||
chr3:32824075 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0006g0286 |
3 | HG02080.hp1 NA19007.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.852+5143A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824075 | |||||||
chr3:32824079 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.852+5147G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824079 | |||||||
chr3:32824187 | T | G | 4 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+5255T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824187 | |||||||
chr3:32824258 | A | C | 3 | a0001c0001t0007g0284 a0001c0003t0005g0285 a0001c0003t0005g0300 |
3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+5326A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824258 | |||||||
chr3:32824265 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.852+5333C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824265 | |||||||
chr3:32824294 | C | A | 2 | a0001c0001t0004g0061 a0001c0002t0002g0062 |
2 | NA18747.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.852+5362C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824294 | |||||||
chr3:32824338 | C | T | 1 | a0001c0001t0028g0220 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.852+5406C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824338 | |||||||
chr3:32824486 | C | T | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.852+5554C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824486 | |||||||
chr3:32824495 | C | T | 2 | a0001c0001t0001g0014 a0001c0003t0005g0024 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+5563C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824495 | |||||||
chr3:32824775 | C | T | 3 | a0001c0001t0003g0225 a0001c0001t0009g0224 a0001c0001t0009g0226 |
3 | HG01069.hp1 HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.852+5843C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824775 | |||||||
chr3:32824792 | C | G | 123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(120): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.852+5860C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824792 | |||||||
chr3:32825097 | T | C | 3 | a0001c0001t0007g0119 a0001c0001t0007g0121 a0001c0003t0005g0120 |
3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.852+6165T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825097 | |||||||
chr3:32825236 | G | A | 1 | a0001c0001t0012g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.852+6304G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825236 | |||||||
chr3:32825293 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.852+6361A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825293 | |||||||
chr3:32825310 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.852+6378C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825310 | |||||||
chr3:32825500 | G | A | 191 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.852+6568G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825500 | |||||||
chr3:32825520 | G | A | 4 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0241 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+6588G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825520 | |||||||
chr3:32825561 | T | C | 3 | a0001c0001t0007g0284 a0001c0003t0005g0285 a0001c0003t0005g0300 |
3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+6629T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825561 | |||||||
chr3:32825612 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(23): Show |
26 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+6680C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825612 | |||||||
chr3:32825633 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+6701T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825633 | |||||||
chr3:32825704 | GATA | G | 3 | a0001c0001t0039g0026 a0001c0003t0005g0027 a0001c0008t0007g0025 |
3 | HG01884.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.852+6775_852+6777d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32825704 | ||||||
chr3:32826186 | C | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+7254C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826186 | |||||||
chr3:32826187 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+7255G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826187 | |||||||
chr3:32826196 | C | T | 4 | a0001c0001t0001g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+7264C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826196 | |||||||
chr3:32826212 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.852+7280A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826212 | |||||||
chr3:32826221 | G | A | 1 | a0001c0001t0006g0130 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.852+7289G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826221 | |||||||
chr3:32826227 | C | T | 1 | a0001c0001t0004g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.852+7295C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826227 | |||||||
chr3:32826398 | A | G | 1 | a0001c0003t0005g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.852+7466A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826398 | |||||||
chr3:32826582 | C | CT | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.852+7672dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | ||||||
chr3:32826582 | C | CTT | 8 | a0001c0001t0001g0214 a0001c0001t0001g0315 a0001c0001t0004g0213 others(5): Show |
8 | HG02738.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.852+7671_852+7672d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | ||||||
chr3:32826582 | C | CTTT | 23 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0064 others(20): Show |
23 | HG00558.hp1 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.852+7670_852+7672d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | ||||||
chr3:32826582 | C | CTTTT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(93): Show |
99 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.852+7669_852+7672d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | ||||||
chr3:32826582 | C | CTTTTT | 42 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(39): Show |
42 | HG00544.hp2 HG01109.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.852+7668_852+7672d others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | ||||||
chr3:32826582 | C | CTTTTTT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0229 others(17): Show |
20 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.852+7667_852+7672d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | ||||||
chr3:32826582 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0010g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.852+7657_852+7672d others(18): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | ||||||
chr3:32826582 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0010g0236 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.852+7672_852+7673i others(37): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | ||||||
chr3:32826582 | C | CTTTTTTT others(30): Show |
1 | a0001c0001t0010g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.852+7672_852+7673i others(39): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | ||||||
chr3:32826608 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.852+7676A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826608 | |||||||
chr3:32826919 | T | C | 28 | a0001c0001t0001g0014 a0001c0001t0008g0227 a0001c0001t0008g0260 others(25): Show |
28 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+7987T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826919 | |||||||
chr3:32826985 | T | C | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+8053T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826985 | |||||||
chr3:32827016 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.852+8084G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827016 | |||||||
chr3:32827192 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+8260C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827192 | |||||||
chr3:32827268 | C | CTTTTTTT others(3): Show |
23 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(20): Show |
23 | HG02074.hp2 HG02080.hp2 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.852+8341_852+8350d others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | ||||||
chr3:32827268 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0027g0277 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.852+8340_852+8350d others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | ||||||
chr3:32827268 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0245 a0001c0001t0001g0248 others(5): Show |
8 | HG01243.hp1 HG01255.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.852+8339_852+8350d others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | ||||||
chr3:32827268 | C | CTTTTTTT others(6): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(16): Show |
19 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.852+8338_852+8350d others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | ||||||
chr3:32827268 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0241 a0001c0001t0029g0255 |
2 | HG01106.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.852+8337_852+8350d others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | ||||||
chr3:32827337 | C | A | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+8405C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827337 | |||||||
chr3:32827489 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(23): Show |
26 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+8557T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827489 | |||||||
chr3:32827782 | G | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(70): Show |
75 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.852+8850G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827782 | |||||||
chr3:32828080 | T | C | 1 | a0001c0002t0002g0059 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.852+9148T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828080 | |||||||
chr3:32828143 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.852+9211A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828143 | |||||||
chr3:32828187 | G | A | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+9255G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828187 | |||||||
chr3:32828229 | T | G | 2 | a0001c0001t0007g0284 a0001c0003t0005g0285 |
2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+9297T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828229 | |||||||
chr3:32828248 | G | A | 4 | a0001c0003t0005g0297 a0001c0003t0005g0298 a0001c0003t0005g0299 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.852+9316G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828248 | |||||||
chr3:32828402 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.852+9470C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828402 | |||||||
chr3:32828430 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0229 others(60): Show |
63 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.852+9498G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828430 | |||||||
chr3:32828458 | A | G | 3 | a0001c0002t0002g0207 a0001c0002t0002g0208 a0001c0002t0025g0209 |
3 | HG00544.hp1 NA19004.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.852+9526A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828458 | |||||||
chr3:32828502 | C | CT | 161 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.852+9593dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32828502 | ||||||
chr3:32828502 | C | CTT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0126 others(21): Show |
25 | HG00609.hp2 HG01106.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.852+9592_852+9593d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32828502 | ||||||
chr3:32828502 | CT | C | 27 | a0001c0001t0001g0014 a0001c0001t0007g0284 a0001c0001t0008g0227 others(24): Show |
27 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.852+9593delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32828502 | ||||||
chr3:32828606 | C | G | 6 | a0001c0001t0003g0225 a0001c0001t0007g0119 a0001c0001t0007g0121 others(3): Show |
6 | HG01069.hp1 HG01123.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+9674C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828606 | |||||||
chr3:32828665 | A | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+9733A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828665 | |||||||
chr3:32828717 | G | A | 1 | a0001c0002t0002g0136 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.852+9785G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828717 | |||||||
chr3:32828815 | A | G | 1 | a0001c0001t0020g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.852+9883A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828815 | |||||||
chr3:32828821 | T | C | 1 | a0001c0001t0026g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852+9889T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828821 | |||||||
chr3:32828868 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+9936G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828868 | |||||||
chr3:32828939 | G | T | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+10007G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828939 | |||||||
chr3:32828953 | T | G | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+10021T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828953 | |||||||
chr3:32828955 | G | C | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+10023G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828955 | |||||||
chr3:32828997 | A | AT | 11 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0113 others(8): Show |
11 | HG00099.hp2 HG01358.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.852+10079dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32828997 | ||||||
chr3:32829033 | G | T | 3 | a0001c0001t0001g0197 a0001c0001t0006g0199 a0001c0002t0002g0198 |
3 | HG00558.hp2 NA18947.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.852+10101G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829033 | |||||||
chr3:32829063 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.852+10131G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829063 | |||||||
chr3:32829149 | A | G | 1 | a0001c0003t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+10217A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829149 | |||||||
chr3:32829168 | TTTTTCTT others(5): Show |
T | 1 | a0001c0002t0047g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.852+10248_852+1025 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829168 | ||||||
chr3:32829185 | CT | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(49): Show |
52 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.852+10269delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829185 | ||||||
chr3:32829235 | A | G | 3 | a0001c0001t0026g0319 a0001c0001t0037g0320 a0001c0003t0005g0321 |
3 | HG02717.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.852+10303A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829235 | |||||||
chr3:32829276 | T | C | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+10344T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829276 | |||||||
chr3:32829341 | C | A | 1 | a0001c0001t0001g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.852+10409C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829341 | |||||||
chr3:32829342 | A | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.852+10410A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829342 | |||||||
chr3:32829505 | T | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(49): Show |
52 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.852+10573T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829505 | |||||||
chr3:32829544 | A | G | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(124): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.852+10612A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829544 | |||||||
chr3:32829561 | A | G | 1 | a0001c0001t0003g0105 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.852+10629A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829561 | |||||||
chr3:32829626 | T | TTG | 9 | a0001c0001t0001g0014 a0001c0001t0001g0302 a0001c0001t0003g0105 others(6): Show |
10 | HG00099.hp1 HG02148.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.852+10718_852+1071 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | T | TTGTG | 12 | a0001c0001t0001g0214 a0001c0001t0003g0189 a0001c0001t0003g0190 others(9): Show |
12 | HG00741.hp1 HG01081.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.852+10716_852+1071 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | T | TTGTGTG | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.852+10714_852+1071 others(10): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0138 a0001c0001t0059g0127 a0001c0002t0002g0288 |
3 | HG00280.hp1 HG01255.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.852+10710_852+1071 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | T | TTGTGTGT others(5): Show |
13 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0245 others(10): Show |
13 | HG00140.hp2 HG00735.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.852+10708_852+1071 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | T | TTGTGTGT others(7): Show |
10 | a0001c0001t0001g0005 a0001c0001t0001g0238 a0001c0001t0001g0239 others(7): Show |
10 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.852+10706_852+1071 others(18): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | T | TTGTGTGT others(9): Show |
16 | a0001c0001t0001g0241 a0001c0001t0008g0260 a0001c0001t0008g0261 others(13): Show |
16 | HG01106.hp1 HG01255.hp2 HG02735.hp1 others(13): Show |
intron_variant | MODIFIER | c.852+10704_852+1071 others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | T | TTGTGTGT others(11): Show |
7 | a0001c0001t0001g0249 a0001c0001t0008g0262 a0001c0001t0008g0266 others(4): Show |
7 | HG01081.hp1 HG01243.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.852+10702_852+1071 others(22): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | T | TTGTGTGT others(13): Show |
2 | a0001c0002t0013g0256 a0001c0002t0013g0264 |
2 | HG02155.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.852+10700_852+1071 others(24): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | T | TTGTGTGT others(19): Show |
1 | a0001c0001t0027g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.852+10719_852+1072 others(30): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | TTG | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0231 a0001c0001t0002g0232 others(12): Show |
15 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.852+10718_852+1071 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829626 | TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0002g0314 others(2): Show |
5 | HG02886.hp2 NA18747.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+10710_852+1071 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | ||||||
chr3:32829651 | T | TGTGTGTG others(14): Show |
1 | a0001c0001t0008g0263 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+10719_852+1072 others(25): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829651 | |||||||
chr3:32829652 | T | G | 5 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(2): Show |
5 | HG00544.hp2 NA18947.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+10720T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829652 | |||||||
chr3:32829654 | G | A | 21 | a0001c0001t0008g0263 a0001c0001t0008g0266 a0001c0001t0008g0271 others(18): Show |
21 | HG02074.hp2 HG02080.hp2 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.852+10722G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829654 | |||||||
chr3:32829659 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0027g0277 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.852+10728_852+1072 others(22): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829659 | ||||||
chr3:32829662 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.852+10730G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829662 | |||||||
chr3:32829733 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.852+10801A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829733 | |||||||
chr3:32829759 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.852+10827C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829759 | |||||||
chr3:32829827 | T | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(49): Show |
52 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.852+10895T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829827 | |||||||
chr3:32829922 | A | AT | 23 | a0001c0001t0001g0125 a0001c0001t0001g0214 a0001c0001t0001g0302 others(20): Show |
24 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.852+11013dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829922 | ||||||
chr3:32829922 | AT | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0001g0141 others(52): Show |
55 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.852+11013delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829922 | ||||||
chr3:32829945 | T | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0139 others(29): Show |
32 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.852+11013T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829945 | |||||||
chr3:32829945 | T | TC | 26 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0035 others(23): Show |
27 | HG01106.hp2 HG01516.hp2 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.852+11014dupC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829945 | ||||||
chr3:32829967 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(23): Show |
26 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+11035C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829967 | |||||||
chr3:32830165 | C | T | 1 | a0001c0001t0017g0278 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.852+11233C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830165 | |||||||
chr3:32830166 | G | A | 3 | a0001c0001t0007g0284 a0001c0003t0005g0285 a0001c0003t0005g0300 |
3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+11234G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830166 | |||||||
chr3:32830277 | C | T | 3 | a0001c0001t0007g0284 a0001c0003t0005g0285 a0001c0003t0005g0300 |
3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+11345C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830277 | |||||||
chr3:32830356 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0229 others(61): Show |
64 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.852+11424C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830356 | |||||||
chr3:32830400 | C | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.852+11468C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830400 | |||||||
chr3:32830454 | A | G | 1 | a0001c0002t0002g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.852+11522A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830454 | |||||||
chr3:32830547 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.852+11615A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830547 | |||||||
chr3:32830654 | A | G | 1 | a0001c0001t0015g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.852+11722A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830654 | |||||||
chr3:32830779 | C | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+11847C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830779 | |||||||
chr3:32830820 | T | A | 1 | a0001c0001t0004g0143 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.852+11888T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830820 | |||||||
chr3:32830821 | T | A | 128 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(125): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.852+11889T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830821 | |||||||
chr3:32830844 | T | C | 2 | a0001c0001t0007g0284 a0001c0003t0005g0285 |
2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+11912T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830844 | |||||||
chr3:32830895 | C | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(23): Show |
26 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+11963C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830895 | |||||||
chr3:32830985 | A | AT | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+12059dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32830985 | ||||||
chr3:32830994 | CAG | C | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+12066_852+1206 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32830994 | ||||||
chr3:32831065 | T | C | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+12133T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831065 | |||||||
chr3:32831080 | G | A | 1 | a0001c0002t0047g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.852+12148G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831080 | |||||||
chr3:32831162 | G | T | 3 | a0001c0001t0001g0002 a0001c0001t0012g0010 a0001c0001t0012g0063 |
4 | HG02615.hp1 HG03195.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+12230G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831162 | |||||||
chr3:32831163 | A | G | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+12231A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831163 | |||||||
chr3:32831308 | TTTCTGAC others(2): Show |
T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(19): Show |
22 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.852+12379_852+1238 others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831308 | ||||||
chr3:32831323 | A | G | 1 | a0001c0003t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+12391A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831323 | |||||||
chr3:32831380 | A | G | 1 | a0001c0001t0019g0324 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.852+12448A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831380 | |||||||
chr3:32831388 | T | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0229 others(51): Show |
54 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.852+12456T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831388 | |||||||
chr3:32831536 | C | CT | 15 | a0001c0001t0001g0014 a0001c0001t0002g0314 a0001c0001t0007g0284 others(12): Show |
15 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.852+12624dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | ||||||
chr3:32831536 | C | CTT | 24 | a0001c0001t0001g0005 a0001c0001t0001g0238 a0001c0001t0001g0239 others(21): Show |
24 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.852+12623_852+1262 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | ||||||
chr3:32831536 | C | CTTT | 25 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0241 others(22): Show |
25 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.852+12622_852+1262 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | ||||||
chr3:32831536 | C | CTTTT | 6 | a0001c0001t0001g0245 a0001c0001t0008g0263 a0001c0001t0008g0274 others(3): Show |
6 | HG01981.hp1 HG02080.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+12621_852+1262 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | ||||||
chr3:32831536 | CT | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.852+12624delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | ||||||
chr3:32831536 | CTT | C | 6 | a0001c0001t0001g0302 a0001c0001t0003g0189 a0001c0001t0004g0057 others(3): Show |
6 | HG01081.hp2 HG01952.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+12623_852+1262 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | ||||||
chr3:32831602 | G | A | 1 | a0001c0001t0039g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.852+12670G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831602 | |||||||
chr3:32831682 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.852+12750G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831682 | |||||||
chr3:32831842 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+12910T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831842 | |||||||
chr3:32831947 | G | A | 1 | a0001c0001t0017g0278 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.852+13015G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831947 | |||||||
chr3:32832100 | T | G | 1 | a0001c0001t0004g0050 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.852+13168T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832100 | |||||||
chr3:32832100 | TG | T | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+13176delG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32832100 | ||||||
chr3:32832101 | G | T | 1 | a0001c0001t0004g0050 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.852+13169G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832101 | |||||||
chr3:32832106 | G | C | 1 | a0001c0003t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+13174G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832106 | |||||||
chr3:32832108 | G | GA | 3 | a0001c0003t0005g0297 a0001c0003t0005g0298 a0001c0003t0005g0299 |
3 | HG01891.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+13177dupA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32832108 | ||||||
chr3:32832124 | A | G | 1 | a0001c0003t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+13192A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832124 | |||||||
chr3:32832413 | C | A | 28 | a0001c0001t0001g0014 a0001c0001t0008g0227 a0001c0001t0008g0260 others(25): Show |
28 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+13481C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832413 | |||||||
chr3:32832470 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.852+13538A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832470 | |||||||
chr3:32832532 | C | A | 28 | a0001c0001t0001g0014 a0001c0001t0008g0227 a0001c0001t0008g0260 others(25): Show |
28 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+13600C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832532 | |||||||
chr3:32832622 | T | G | 1 | a0001c0001t0001g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+13690T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832622 | |||||||
chr3:32832692 | A | G | 17 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0089 others(14): Show |
17 | HG00609.hp1 HG01109.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.852+13760A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832692 | |||||||
chr3:32832944 | A | G | 5 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0042g0107 others(2): Show |
5 | HG03491.hp2 HG03710.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+14012A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832944 | |||||||
chr3:32833045 | C | A | 1 | a0001c0002t0002g0145 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.852+14113C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833045 | |||||||
chr3:32833058 | C | A | 2 | a0001c0001t0008g0266 a0001c0002t0013g0264 |
2 | HG02074.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.852+14126C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833058 | |||||||
chr3:32833067 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0181 others(6): Show |
9 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.852+14135C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833067 | |||||||
chr3:32833077 | A | T | 3 | a0001c0001t0007g0284 a0001c0003t0005g0285 a0001c0003t0005g0300 |
3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+14145A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833077 | |||||||
chr3:32833183 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.852+14251T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833183 | |||||||
chr3:32833184 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.852+14252T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833184 | |||||||
chr3:32833184 | T | TA | 72 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0075 others(69): Show |
73 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.852+14280dupA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0086 others(21): Show |
24 | HG01358.hp1 HG01516.hp2 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.852+14279_852+1428 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(25): Show |
28 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+14278_852+1428 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAA | 12 | a0001c0001t0001g0054 a0001c0001t0003g0056 a0001c0001t0003g0171 others(9): Show |
12 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.852+14277_852+1428 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAA | 10 | a0001c0001t0001g0214 a0001c0001t0003g0188 a0001c0001t0003g0192 others(7): Show |
10 | HG00597.hp1 HG01516.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.852+14276_852+1428 others(9): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(3): Show |
3 | a0001c0001t0006g0012 a0001c0001t0009g0226 a0001c0003t0005g0299 |
3 | HG01069.hp1 HG02165.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+14271_852+1428 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(4): Show |
10 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0004g0168 others(7): Show |
10 | HG00621.hp2 HG01123.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.852+14270_852+1428 others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(5): Show |
15 | a0001c0001t0001g0197 a0001c0001t0003g0225 a0001c0002t0002g0146 others(12): Show |
15 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.852+14269_852+1428 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0009 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.852+14268_852+1428 others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(8): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0123 a0001c0001t0001g0125 |
3 | NA18969.hp1 NA18975.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.852+14266_852+1428 others(19): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0196 a0001c0001t0001g0210 a0001c0002t0002g0124 others(1): Show |
4 | HG01884.hp2 HG03710.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+14265_852+1428 others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(10): Show |
4 | a0001c0001t0001g0007 a0001c0001t0004g0157 a0001c0001t0012g0169 others(1): Show |
4 | HG00423.hp1 HG00621.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.852+14264_852+1428 others(21): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(11): Show |
1 | a0001c0001t0031g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.852+14263_852+1428 others(22): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(13): Show |
1 | a0001c0001t0006g0286 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.852+14261_852+1428 others(24): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0001g0222 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.852+14260_852+1428 others(25): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(16): Show |
2 | a0001c0002t0002g0198 a0001c0002t0002g0205 |
2 | HG02027.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.852+14258_852+1428 others(27): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(17): Show |
2 | a0001c0001t0019g0195 a0001c0002t0002g0215 |
2 | NA18979.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.852+14257_852+1428 others(28): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(18): Show |
2 | a0001c0001t0001g0126 a0001c0001t0006g0167 |
2 | HG02015.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.852+14256_852+1428 others(29): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(19): Show |
2 | a0001c0001t0001g0221 a0001c0002t0002g0183 |
2 | HG02080.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.852+14255_852+1428 others(30): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(21): Show |
2 | a0001c0001t0001g0158 a0001c0001t0033g0179 |
2 | HG02056.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.852+14253_852+1428 others(32): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(24): Show |
1 | a0001c0002t0024g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.852+14280_852+1428 others(35): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | T | TAAAAAAA others(28): Show |
1 | a0001c0001t0006g0199 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.852+14280_852+1428 others(39): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | TA | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0001g0162 others(9): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.852+14280delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | TAA | T | 20 | a0001c0001t0001g0138 a0001c0001t0007g0098 a0001c0001t0007g0284 others(17): Show |
20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.852+14279_852+1428 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | TAAA | T | 23 | a0001c0001t0001g0173 a0001c0001t0001g0187 a0001c0001t0008g0227 others(20): Show |
23 | HG00544.hp2 HG02080.hp2 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.852+14278_852+1428 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0001g0131 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG01934.hp1 HG01981.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.852+14273_852+1428 others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833184 | TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0014 a0001c0003t0005g0024 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+14271_852+1428 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | ||||||
chr3:32833213 | G | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+14281G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833213 | |||||||
chr3:32833294 | G | A | 1 | a0001c0002t0002g0146 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.852+14362G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833294 | |||||||
chr3:32833414 | G | T | 26 | a0001c0001t0008g0227 a0001c0001t0008g0260 a0001c0001t0008g0261 others(23): Show |
26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+14482G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833414 | |||||||
chr3:32833634 | T | TTTTA | 77 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0035 others(74): Show |
78 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.852+14742_852+1474 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | ||||||
chr3:32833634 | T | TTTTATTT others(1): Show |
31 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0001t0001g0085 others(28): Show |
31 | HG00280.hp2 HG01261.hp1 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.852+14738_852+1474 others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | ||||||
chr3:32833634 | T | TTTTATTT others(5): Show |
5 | a0001c0001t0001g0075 a0001c0001t0002g0074 a0001c0001t0017g0257 others(2): Show |
5 | HG03471.hp1 HG03471.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+14734_852+1474 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | ||||||
chr3:32833634 | TTTTA | T | 19 | a0001c0001t0001g0203 a0001c0001t0001g0231 a0001c0001t0001g0247 others(16): Show |
21 | HG01069.hp1 HG01123.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.852+14742_852+1474 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | ||||||
chr3:32833634 | TTTTATTT others(5): Show |
T | 5 | a0001c0001t0003g0094 a0001c0001t0004g0142 a0001c0001t0004g0213 others(2): Show |
5 | HG02572.hp1 HG03669.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+14734_852+1474 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | ||||||
chr3:32833734 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.852+14802G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833734 | |||||||
chr3:32833785 | T | G | 2 | a0001c0001t0001g0014 a0001c0003t0005g0024 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+14853T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833785 | |||||||
chr3:32834034 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.852+15102T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834034 | |||||||
chr3:32834394 | A | AGTT | 28 | a0001c0001t0001g0014 a0001c0001t0008g0227 a0001c0001t0008g0260 others(25): Show |
28 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+15463_852+1546 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32834394 | ||||||
chr3:32834523 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.852+15591G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834523 | |||||||
chr3:32834546 | G | C | 2 | a0001c0002t0002g0289 a0001c0002t0002g0295 |
2 | NA18977.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.852+15614G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834546 | |||||||
chr3:32834662 | T | A | 1 | a0001c0001t0007g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.852+15730T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834662 | |||||||
chr3:32834694 | T | G | 1 | a0001c0001t0002g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.852+15762T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834694 | |||||||
chr3:32834714 | C | T | 1 | a0001c0001t0003g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.852+15782C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834714 | |||||||
chr3:32834750 | G | C | 3 | a0001c0001t0039g0026 a0001c0003t0005g0027 a0001c0008t0007g0025 |
3 | HG01884.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.852+15818G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834750 | |||||||
chr3:32834798 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.852+15866C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834798 | |||||||
chr3:32834876 | T | C | 3 | a0001c0001t0039g0026 a0001c0003t0005g0027 a0001c0008t0007g0025 |
3 | HG01884.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.852+15944T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834876 | |||||||
chr3:32834916 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.852+15984C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834916 | |||||||
chr3:32834919 | A | G | 1 | a0001c0001t0014g0280 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.852+15987A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834919 | |||||||
chr3:32834946 | C | T | 3 | a0001c0001t0007g0119 a0001c0001t0007g0121 a0001c0003t0005g0120 |
3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.852+16014C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834946 | |||||||
chr3:32835196 | C | A | 47 | a0001c0001t0001g0014 a0001c0001t0004g0036 a0001c0001t0004g0037 others(44): Show |
47 | HG00544.hp2 HG01109.hp2 HG02040.hp2 others(44): Show |
intron_variant | MODIFIER | c.852+16264C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835196 | |||||||
chr3:32835247 | T | C | 23 | a0001c0001t0001g0138 a0001c0001t0001g0229 a0001c0001t0001g0230 others(20): Show |
23 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.852+16315T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835247 | |||||||
chr3:32835394 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.852+16462G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835394 | |||||||
chr3:32835794 | T | G | 6 | a0001c0001t0017g0257 a0001c0001t0017g0258 a0001c0001t0053g0269 others(3): Show |
6 | NA18962.hp1 NA19003.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+16862T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835794 | |||||||
chr3:32835830 | C | CT | 126 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(123): Show |
128 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.852+16898_852+1689 others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835830 | |||||||
chr3:32835831 | G | A | 1 | a0001c0002t0002g0039 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.852+16899G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835831 | |||||||
chr3:32835868 | G | A | 1 | a0001c0003t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+16936G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835868 | |||||||
chr3:32835933 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.852+17001T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835933 | |||||||
chr3:32836073 | C | G | 1 | a0001c0001t0001g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.852+17141C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836073 | |||||||
chr3:32836160 | G | A | 1 | a0001c0002t0002g0062 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.852+17228G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836160 | |||||||
chr3:32836337 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.852+17405T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836337 | |||||||
chr3:32836411 | A | G | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+17479A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836411 | |||||||
chr3:32836642 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.852+17710C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836642 | |||||||
chr3:32836648 | T | A | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.852+17716T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836648 | |||||||
chr3:32836667 | G | T | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+17735G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836667 | |||||||
chr3:32836779 | A | C | 3 | a0001c0002t0002g0207 a0001c0002t0002g0208 a0001c0002t0025g0209 |
3 | HG00544.hp1 NA19004.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.852+17847A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836779 | |||||||
chr3:32836819 | A | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(75): Show |
80 | HG00099.hp2 HG00609.hp1 HG01109.hp1 others(77): Show |
intron_variant | MODIFIER | c.852+17887A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836819 | |||||||
chr3:32836939 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.852+18007T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836939 | |||||||
chr3:32836941 | C | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+18009C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836941 | |||||||
chr3:32837100 | AAAC | A | 56 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0229 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.852+18175_852+1817 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32837100 | ||||||
chr3:32837182 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.852+18250G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837182 | |||||||
chr3:32837190 | T | C | 56 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0229 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.852+18258T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837190 | |||||||
chr3:32837426 | G | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+18494G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837426 | |||||||
chr3:32837427 | T | G | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+18495T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837427 | |||||||
chr3:32837482 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.852+18550G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837482 | |||||||
chr3:32837690 | G | A | 3 | a0001c0001t0007g0284 a0001c0003t0005g0285 a0001c0003t0005g0300 |
3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+18758G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837690 | |||||||
chr3:32837813 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.852+18881G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837813 | |||||||
chr3:32837813 | GA | G | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(122): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.852+18889delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32837813 | ||||||
chr3:32837814 | A | G | 1 | a0001c0001t0003g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.852+18882A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837814 | |||||||
chr3:32838004 | G | T | 2 | a0001c0001t0006g0286 a0001c0002t0002g0198 |
2 | NA18982.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.852+19072G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838004 | |||||||
chr3:32838022 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.852+19090A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838022 | |||||||
chr3:32838023 | C | T | 1 | a0001c0001t0004g0149 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.852+19091C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838023 | |||||||
chr3:32838049 | G | A | 1 | a0001c0002t0025g0147 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.852+19117G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838049 | |||||||
chr3:32838071 | G | A | 1 | a0001c0001t0006g0212 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.852+19139G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838071 | |||||||
chr3:32838171 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(116): Show |
122 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.852+19239T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838171 | |||||||
chr3:32838233 | A | G | 3 | a0001c0001t0007g0284 a0001c0003t0005g0285 a0001c0003t0005g0300 |
3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+19301A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838233 | |||||||
chr3:32838254 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.852+19322A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838254 | |||||||
chr3:32838271 | TGGAGTGC others(22): Show |
T | 1 | a0001c0001t0008g0263 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+19340_852+1936 others(33): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838271 | |||||||
chr3:32838331 | A | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0229 others(58): Show |
61 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.852+19399A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838331 | |||||||
chr3:32838461 | G | A | 1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.852+19529G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838461 | |||||||
chr3:32838522 | C | CT | 83 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(80): Show |
85 | HG00099.hp2 HG00609.hp1 HG01109.hp1 others(82): Show |
intron_variant | MODIFIER | c.852+19608dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32838522 | ||||||
chr3:32838522 | CT | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0076 others(25): Show |
28 | HG00140.hp2 HG00735.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.852+19608delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32838522 | ||||||
chr3:32838522 | CTT | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.852+19607_852+1960 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32838522 | ||||||
chr3:32838586 | G | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.852+19654G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838586 | |||||||
chr3:32838623 | T | C | 33 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(30): Show |
33 | HG00280.hp2 HG00544.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.852+19691T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838623 | |||||||
chr3:32838692 | T | C | 5 | a0001c0001t0007g0284 a0001c0002t0047g0101 a0001c0003t0005g0024 others(2): Show |
5 | HG02572.hp1 HG02683.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+19760T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838692 | |||||||
chr3:32838771 | C | G | 33 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(30): Show |
33 | HG00280.hp2 HG00544.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.852+19839C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838771 | |||||||
chr3:32838832 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.852+19900G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838832 | |||||||
chr3:32838834 | T | A | 1 | a0001c0001t0003g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.852+19902T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838834 | |||||||
chr3:32838838 | T | A | 1 | a0001c0001t0003g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.852+19906T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838838 | |||||||
chr3:32838893 | C | T | 4 | a0001c0001t0001g0131 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG01934.hp1 HG01981.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+19961C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838893 | |||||||
chr3:32838976 | T | C | 1 | a0001c0001t0027g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.852+20044T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838976 | |||||||
chr3:32839073 | C | T | 1 | a0001c0001t0021g0174 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.852+20141C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839073 | |||||||
chr3:32839353 | C | T | 1 | a0001c0003t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+20421C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839353 | |||||||
chr3:32839479 | C | T | 3 | a0001c0001t0002g0083 a0001c0001t0018g0099 a0001c0003t0005g0084 |
3 | HG02145.hp1 HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.852+20547C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839479 | |||||||
chr3:32839506 | A | G | 38 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(35): Show |
38 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(35): Show |
intron_variant | MODIFIER | c.852+20574A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839506 | |||||||
chr3:32839550 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.852+20618A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839550 | |||||||
chr3:32839639 | G | A | 1 | a0001c0001t0016g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.852+20707G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839639 | |||||||
chr3:32839654 | CT | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(17): Show |
20 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.852+20729delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32839654 | ||||||
chr3:32839661 | T | TG | 28 | a0001c0001t0002g0083 a0001c0001t0003g0112 a0001c0001t0004g0036 others(25): Show |
28 | HG00280.hp2 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+20739dupG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32839661 | ||||||
chr3:32839661 | TG | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.852+20739delG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32839661 | ||||||
chr3:32839667 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.852+20735G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839667 | |||||||
chr3:32839668 | G | T | 3 | a0001c0003t0005g0297 a0001c0003t0005g0298 a0001c0003t0005g0299 |
3 | HG01891.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+20736G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839668 | |||||||
chr3:32839748 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0009g0148 |
2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.852+20816C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839748 | |||||||
chr3:32839861 | C | T | 1 | a0001c0001t0009g0148 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.852+20929C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839861 | |||||||
chr3:32839975 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.852+21043T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839975 | |||||||
chr3:32840014 | A | C | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+21082A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840014 | |||||||
chr3:32840086 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.852+21154C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840086 | |||||||
chr3:32840125 | A | C | 2 | a0001c0001t0002g0067 a0001c0001t0002g0082 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.852+21193A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840125 | |||||||
chr3:32840157 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+21225A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840157 | |||||||
chr3:32840179 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.852+21247A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840179 | |||||||
chr3:32840183 | CAGGGAGG others(5): Show |
C | 1 | a0001c0002t0002g0215 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.852+21253_852+2126 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32840183 | ||||||
chr3:32840515 | G | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(117): Show |
120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.852+21583G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840515 | |||||||
chr3:32840516 | A | G | 8 | a0001c0001t0001g0131 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01934.hp1 HG01981.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.852+21584A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840516 | |||||||
chr3:32840651 | T | C | 1 | a0001c0002t0002g0322 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.852+21719T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840651 | |||||||
chr3:32840701 | G | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+21769G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840701 | |||||||
chr3:32840711 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.852+21779C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840711 | |||||||
chr3:32840779 | C | CACTGGTG | 22 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0230 others(19): Show |
22 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.852+21849_852+2185 others(11): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32840779 | ||||||
chr3:32840844 | G | C | 1 | a0001c0001t0004g0149 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.852+21912G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840844 | |||||||
chr3:32841138 | G | A | 1 | a0001c0003t0005g0297 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.852+22206G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841138 | |||||||
chr3:32841200 | G | A | 1 | a0001c0001t0014g0280 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.852+22268G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841200 | |||||||
chr3:32841354 | G | T | 1 | a0001c0001t0008g0263 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+22422G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841354 | |||||||
chr3:32841370 | A | G | 34 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(31): Show |
34 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.852+22438A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841370 | |||||||
chr3:32841542 | C | T | 1 | a0001c0001t0034g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.852+22610C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841542 | |||||||
chr3:32841551 | T | C | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+22619T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841551 | |||||||
chr3:32841591 | G | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.852+22659G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841591 | |||||||
chr3:32841618 | A | C | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+22686A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841618 | |||||||
chr3:32841623 | C | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+22691C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841623 | |||||||
chr3:32841624 | A | C | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+22692A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841624 | |||||||
chr3:32841629 | C | G | 1 | a0001c0002t0013g0265 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.852+22697C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841629 | |||||||
chr3:32841697 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.852+22765G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841697 | |||||||
chr3:32841722 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.852+22790G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841722 | |||||||
chr3:32841769 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.852+22837C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841769 | |||||||
chr3:32841785 | A | G | 1 | a0001c0002t0002g0215 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.852+22853A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841785 | |||||||
chr3:32841834 | A | T | 1 | a0001c0001t0008g0276 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.852+22902A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841834 | |||||||
chr3:32841883 | A | G | 1 | a0001c0001t0004g0149 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.852+22951A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841883 | |||||||
chr3:32841917 | C | T | 34 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(31): Show |
34 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.852+22985C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841917 | |||||||
chr3:32842089 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.852+23157G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842089 | |||||||
chr3:32842104 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(176): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.852+23172G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842104 | |||||||
chr3:32842269 | A | C | 1 | a0001c0001t0002g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.852+23337A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842269 | |||||||
chr3:32842429 | A | G | 3 | a0001c0001t0002g0303 a0001c0001t0002g0306 a0001c0001t0002g0307 |
3 | HG02451.hp1 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.852+23497A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842429 | |||||||
chr3:32842546 | C | T | 4 | a0001c0001t0001g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+23614C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842546 | |||||||
chr3:32842587 | C | T | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.852+23655C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842587 | |||||||
chr3:32842699 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.852+23767A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842699 | |||||||
chr3:32842720 | TACAG | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.852+23793_852+2379 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32842720 | ||||||
chr3:32842740 | G | A | 1 | a0001c0002t0002g0062 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.852+23808G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842740 | |||||||
chr3:32842761 | A | C | 1 | a0001c0001t0008g0263 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+23829A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842761 | |||||||
chr3:32842861 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.852+23929C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842861 | |||||||
chr3:32843016 | G | C | 1 | a0001c0001t0008g0263 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+24084G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843016 | |||||||
chr3:32843017 | C | G | 1 | a0001c0001t0008g0263 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+24085C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843017 | |||||||
chr3:32843018 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0082 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.852+24086G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843018 | |||||||
chr3:32843228 | C | G | 1 | a0001c0001t0016g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.852+24296C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843228 | |||||||
chr3:32843254 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0241 a0001c0001t0001g0245 others(15): Show |
18 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.852+24322G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843254 | |||||||
chr3:32843365 | G | A | 1 | a0001c0001t0057g0270 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.852+24433G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843365 | |||||||
chr3:32843457 | G | A | 3 | a0001c0003t0005g0297 a0001c0003t0005g0298 a0001c0003t0005g0299 |
3 | HG01891.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+24525G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843457 | |||||||
chr3:32843575 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+24643C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843575 | |||||||
chr3:32843815 | A | G | 1 | a0001c0001t0006g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.852+24883A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843815 | |||||||
chr3:32844043 | C | T | 2 | a0001c0001t0018g0281 a0001c0003t0005g0024 |
2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.852+25111C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844043 | |||||||
chr3:32844092 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.852+25160C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844092 | |||||||
chr3:32844100 | G | T | 33 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(30): Show |
33 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(30): Show |
intron_variant | MODIFIER | c.852+25168G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844100 | |||||||
chr3:32844111 | G | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0241 a0001c0001t0001g0245 others(24): Show |
27 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.852+25179G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844111 | |||||||
chr3:32844113 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.852+25181G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844113 | |||||||
chr3:32844491 | G | C | 46 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0054 others(43): Show |
46 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.852+25559G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844491 | |||||||
chr3:32844503 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.852+25571C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844503 | |||||||
chr3:32844518 | T | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(53): Show |
59 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+25586T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844518 | |||||||
chr3:32844519 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(53): Show |
59 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+25587C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844519 | |||||||
chr3:32844717 | A | G | 1 | a0001c0002t0002g0062 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.852+25785A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844717 | |||||||
chr3:32844835 | A | G | 1 | a0001c0001t0004g0213 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.852+25903A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844835 | |||||||
chr3:32844903 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.852+25971C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844903 | |||||||
chr3:32844944 | T | G | 29 | a0001c0001t0001g0005 a0001c0001t0001g0238 a0001c0001t0001g0239 others(26): Show |
29 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.852+26012T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844944 | |||||||
chr3:32844954 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(167): Show |
173 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.852+26022G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844954 | |||||||
chr3:32845127 | CCTGGAGG others(16): Show |
C | 5 | a0001c0003t0005g0097 a0001c0003t0005g0297 a0001c0003t0005g0298 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+26201_852+2622 others(27): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32845127 | ||||||
chr3:32845141 | A | G | 1 | a0001c0001t0004g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.852+26209A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845141 | |||||||
chr3:32845172 | A | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(317): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.852+26240A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845172 | |||||||
chr3:32845252 | G | C | 1 | a0001c0002t0002g0124 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.852+26320G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845252 | |||||||
chr3:32845502 | A | C | 1 | a0001c0007t0012g0133 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.852+26570A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845502 | |||||||
chr3:32845533 | G | T | 1 | a0001c0001t0019g0324 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.852+26601G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845533 | |||||||
chr3:32845602 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.852+26670T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845602 | |||||||
chr3:32845608 | A | T | 2 | a0001c0001t0002g0317 a0001c0001t0002g0318 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.852+26676A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845608 | |||||||
chr3:32845663 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(54): Show |
60 | HG00099.hp2 HG01081.hp1 HG01261.hp1 others(57): Show |
intron_variant | MODIFIER | c.852+26731A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845663 | |||||||
chr3:32845688 | A | G | 5 | a0001c0003t0005g0097 a0001c0003t0005g0297 a0001c0003t0005g0298 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+26756A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845688 | |||||||
chr3:32845697 | C | T | 1 | a0001c0001t0040g0254 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.852+26765C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845697 | |||||||
chr3:32845718 | CT | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(293): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.852+26799delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32845718 | ||||||
chr3:32845757 | G | C | 3 | a0001c0001t0007g0119 a0001c0001t0007g0121 a0001c0003t0005g0120 |
3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.852+26825G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845757 | |||||||
chr3:32845844 | C | G | 1 | a0001c0001t0040g0254 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.852+26912C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845844 | |||||||
chr3:32845934 | T | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(55): Show |
61 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(58): Show |
intron_variant | MODIFIER | c.852+27002T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845934 | |||||||
chr3:32846000 | TG | T | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
109 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.852+27070delG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846000 | ||||||
chr3:32846036 | T | C | 1 | a0001c0001t0027g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.852+27104T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846036 | |||||||
chr3:32846072 | CT | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.852+27161delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846072 | ||||||
chr3:32846072 | CTT | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0113 others(25): Show |
29 | HG01109.hp2 HG01358.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.852+27160_852+2716 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846072 | ||||||
chr3:32846072 | CTTT | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
161 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.852+27159_852+2716 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846072 | ||||||
chr3:32846121 | G | C | 5 | a0001c0003t0005g0097 a0001c0003t0005g0297 a0001c0003t0005g0298 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+27189G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846121 | |||||||
chr3:32846171 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.852+27239G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846171 | |||||||
chr3:32846221 | G | A | 1 | a0001c0001t0042g0107 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.852+27289G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846221 | |||||||
chr3:32846345 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0009g0148 |
2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.852+27413G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846345 | |||||||
chr3:32846428 | A | G | 2 | a0001c0001t0018g0281 a0001c0001t0039g0026 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.853-27390A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846428 | |||||||
chr3:32846494 | T | C | 3 | a0001c0001t0001g0302 a0001c0001t0016g0003 a0001c0003t0005g0027 |
4 | HG01934.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-27324T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846494 | |||||||
chr3:32846573 | G | C | 2 | a0001c0001t0002g0317 a0001c0001t0002g0318 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853-27245G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846573 | |||||||
chr3:32846609 | C | G | 2 | a0001c0001t0001g0249 a0001c0001t0007g0308 |
2 | HG01081.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.853-27209C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846609 | |||||||
chr3:32846610 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.853-27208T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846610 | |||||||
chr3:32846713 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.853-27105A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846713 | |||||||
chr3:32846763 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.853-27055A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846763 | |||||||
chr3:32846851 | G | A | 1 | a0001c0001t0012g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.853-26967G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846851 | |||||||
chr3:32846991 | T | TG | 34 | a0001c0001t0001g0005 a0001c0001t0001g0238 a0001c0001t0001g0239 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.853-26823dupG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846991 | ||||||
chr3:32846994 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.853-26824G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846994 | |||||||
chr3:32847190 | A | AT | 19 | a0001c0001t0001g0302 a0001c0001t0002g0118 a0001c0001t0002g0232 others(16): Show |
19 | HG01123.hp1 HG01192.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.853-26605dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32847190 | ||||||
chr3:32847190 | A | ATT | 8 | a0001c0001t0001g0110 a0001c0001t0001g0231 a0001c0001t0001g0245 others(5): Show |
8 | HG01981.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-26606_853-2660 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32847190 | ||||||
chr3:32847190 | AT | A | 150 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(147): Show |
150 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.853-26605delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32847190 | ||||||
chr3:32847190 | ATT | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0196 others(8): Show |
11 | HG01081.hp1 HG01123.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.853-26606_853-2660 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32847190 | ||||||
chr3:32847197 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.853-26621T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847197 | |||||||
chr3:32847273 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(61): Show |
66 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(63): Show |
intron_variant | MODIFIER | c.853-26545C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847273 | |||||||
chr3:32847288 | C | G | 1 | a0001c0001t0003g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.853-26530C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847288 | |||||||
chr3:32847359 | G | A | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(104): Show |
107 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.853-26459G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847359 | |||||||
chr3:32847387 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0141 |
2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.853-26431G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847387 | |||||||
chr3:32847437 | C | T | 32 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(29): Show |
32 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.853-26381C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847437 | |||||||
chr3:32847484 | C | T | 1 | a0001c0001t0007g0312 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.853-26334C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847484 | |||||||
chr3:32847551 | G | A | 1 | a0001c0001t0006g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.853-26267G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847551 | |||||||
chr3:32847606 | A | G | 14 | a0001c0001t0001g0197 a0001c0001t0003g0094 a0001c0001t0004g0061 others(11): Show |
14 | HG00558.hp2 HG00609.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.853-26212A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847606 | |||||||
chr3:32847646 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.853-26172T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847646 | |||||||
chr3:32847662 | G | T | 1 | a0001c0001t0004g0294 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.853-26156G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847662 | |||||||
chr3:32847717 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0009g0240 |
2 | HG01106.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.853-26101T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847717 | |||||||
chr3:32847822 | G | A | 1 | a0001c0001t0018g0281 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853-25996G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847822 | |||||||
chr3:32847869 | G | A | 5 | a0001c0003t0005g0097 a0001c0003t0005g0297 a0001c0003t0005g0298 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-25949G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847869 | |||||||
chr3:32847948 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(66): Show |
71 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(68): Show |
intron_variant | MODIFIER | c.853-25870A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847948 | |||||||
chr3:32848146 | C | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0181 a0001c0001t0001g0238 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.853-25672C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848146 | |||||||
chr3:32848476 | A | G | 32 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(29): Show |
32 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.853-25342A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848476 | |||||||
chr3:32848479 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.853-25339A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848479 | |||||||
chr3:32848494 | G | A | 3 | a0001c0001t0045g0071 a0001c0002t0002g0070 a0001c0003t0005g0117 |
3 | HG02630.hp1 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.853-25324G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848494 | |||||||
chr3:32848503 | G | A | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.853-25315G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848503 | |||||||
chr3:32848581 | G | C | 4 | a0001c0002t0002g0287 a0001c0002t0002g0291 a0001c0002t0002g0292 others(1): Show |
4 | NA18945.hp2 NA18973.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-25237G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848581 | |||||||
chr3:32848613 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.853-25205C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848613 | |||||||
chr3:32848627 | A | G | 5 | a0001c0001t0001g0178 a0001c0001t0001g0210 a0001c0002t0002g0106 others(2): Show |
5 | HG00639.hp2 HG01261.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-25191A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848627 | |||||||
chr3:32848710 | C | G | 2 | a0001c0001t0014g0246 a0001c0001t0014g0250 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.853-25108C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848710 | |||||||
chr3:32848822 | C | A | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.853-24996C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848822 | |||||||
chr3:32848940 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-24878A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848940 | |||||||
chr3:32848998 | A | G | 2 | a0001c0001t0007g0284 a0001c0003t0005g0285 |
2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.853-24820A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848998 | |||||||
chr3:32849203 | C | G | 37 | a0001c0001t0001g0030 a0001c0001t0001g0231 a0001c0001t0001g0247 others(34): Show |
37 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.853-24615C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849203 | |||||||
chr3:32849225 | T | C | 5 | a0001c0003t0005g0097 a0001c0003t0005g0297 a0001c0003t0005g0298 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-24593T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849225 | |||||||
chr3:32849276 | C | T | 1 | a0001c0004t0011g0243 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.853-24542C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849276 | |||||||
chr3:32849518 | C | A | 106 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.853-24300C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849518 | |||||||
chr3:32849617 | C | T | 1 | a0001c0001t0018g0281 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853-24201C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849617 | |||||||
chr3:32849699 | T | TTG | 12 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0110 others(9): Show |
12 | HG01884.hp2 HG01934.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.853-24118_853-2411 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32849699 | ||||||
chr3:32849784 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0231 a0001c0001t0001g0247 others(2): Show |
5 | HG02258.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-24034C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849784 | |||||||
chr3:32849834 | A | G | 2 | a0001c0001t0002g0317 a0001c0001t0002g0318 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853-23984A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849834 | |||||||
chr3:32849931 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0181 a0001c0001t0001g0238 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.853-23887A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849931 | |||||||
chr3:32850017 | T | C | 5 | a0001c0003t0005g0097 a0001c0003t0005g0297 a0001c0003t0005g0298 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-23801T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850017 | |||||||
chr3:32850112 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.853-23706C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850112 | |||||||
chr3:32850265 | A | AT | 54 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0138 others(51): Show |
54 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.853-23544dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32850265 | ||||||
chr3:32850273 | T | G | 2 | a0001c0001t0001g0249 a0001c0001t0003g0251 |
2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.853-23545T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850273 | |||||||
chr3:32850275 | G | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0030 others(56): Show |
61 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(58): Show |
intron_variant | MODIFIER | c.853-23543G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850275 | |||||||
chr3:32850947 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(53): Show |
58 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(55): Show |
intron_variant | MODIFIER | c.853-22871G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850947 | |||||||
chr3:32850968 | T | C | 1 | a0001c0001t0034g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.853-22850T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850968 | |||||||
chr3:32850971 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(62): Show |
67 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(64): Show |
intron_variant | MODIFIER | c.853-22847A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850971 | |||||||
chr3:32851143 | G | A | 5 | a0001c0001t0003g0094 a0001c0001t0009g0115 a0001c0001t0050g0095 others(2): Show |
5 | HG01109.hp1 HG02683.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-22675G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851143 | |||||||
chr3:32851512 | C | G | 4 | a0001c0001t0001g0231 a0001c0001t0001g0247 a0001c0001t0002g0233 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-22306C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851512 | |||||||
chr3:32851559 | A | G | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-22259A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851559 | |||||||
chr3:32851562 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.853-22256G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851562 | |||||||
chr3:32851593 | C | T | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.853-22225C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851593 | |||||||
chr3:32851602 | C | T | 1 | a0001c0001t0012g0010 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.853-22216C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851602 | |||||||
chr3:32851604 | G | A | 1 | a0001c0001t0016g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.853-22214G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851604 | |||||||
chr3:32851622 | G | T | 1 | a0001c0002t0002g0288 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.853-22196G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851622 | |||||||
chr3:32851626 | C | T | 1 | a0001c0002t0002g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.853-22192C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851626 | |||||||
chr3:32851627 | C | A | 2 | a0001c0002t0002g0205 a0001c0002t0002g0288 |
2 | HG02027.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.853-22191C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851627 | |||||||
chr3:32851848 | T | C | 4 | a0001c0001t0001g0302 a0001c0001t0002g0118 a0001c0001t0002g0172 others(1): Show |
4 | HG01934.hp2 HG02896.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-21970T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851848 | |||||||
chr3:32851954 | T | C | 1 | a0001c0002t0046g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.853-21864T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851954 | |||||||
chr3:32852055 | G | T | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-21763G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852055 | |||||||
chr3:32852279 | C | A | 2 | a0001c0002t0002g0322 a0001c0003t0005g0321 |
2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.853-21539C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852279 | |||||||
chr3:32852279 | C | G | 1 | a0001c0008t0007g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853-21539C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852279 | |||||||
chr3:32852353 | G | C | 1 | a0001c0002t0002g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.853-21465G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852353 | |||||||
chr3:32852363 | C | CT | 4 | a0001c0001t0001g0076 a0001c0001t0002g0074 a0001c0001t0002g0077 others(1): Show |
4 | HG02970.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-21454dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32852363 | ||||||
chr3:32852466 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853-21352C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852466 | |||||||
chr3:32852759 | T | A | 2 | a0001c0001t0018g0281 a0001c0002t0002g0015 |
2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-21059T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852759 | |||||||
chr3:32852759 | T | TA | 181 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(178): Show |
181 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.853-21044dupA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32852759 | ||||||
chr3:32852759 | T | TAA | 12 | a0001c0001t0001g0006 a0001c0001t0048g0152 a0001c0002t0002g0016 others(9): Show |
12 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.853-21045_853-2104 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32852759 | ||||||
chr3:32852759 | TA | T | 13 | a0001c0001t0001g0315 a0001c0001t0002g0303 a0001c0001t0002g0306 others(10): Show |
14 | HG00639.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.853-21044delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32852759 | ||||||
chr3:32852768 | A | AC | 5 | a0001c0001t0001g0030 a0001c0001t0001g0231 a0001c0001t0001g0247 others(2): Show |
5 | HG02258.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-21050_853-2104 others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852768 | |||||||
chr3:32852769 | A | AC | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(53): Show |
58 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(55): Show |
intron_variant | MODIFIER | c.853-21049_853-2104 others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852769 | |||||||
chr3:32852868 | A | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0231 a0001c0001t0001g0247 others(2): Show |
5 | HG02258.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-20950A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852868 | |||||||
chr3:32853104 | TTC | T | 3 | a0001c0001t0001g0125 a0001c0002t0002g0122 a0001c0002t0002g0124 |
3 | NA18948.hp1 NA18968.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.853-20698_853-2069 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853104 | ||||||
chr3:32853118 | CTCT | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(212): Show |
217 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.853-20698_853-2069 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853118 | ||||||
chr3:32853120 | CT | C | 17 | a0001c0001t0001g0315 a0001c0001t0002g0303 a0001c0001t0002g0306 others(14): Show |
18 | HG00639.hp1 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.853-20682delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853120 | ||||||
chr3:32853120 | CTT | C | 45 | a0001c0001t0001g0030 a0001c0001t0001g0110 a0001c0001t0001g0231 others(42): Show |
45 | HG00544.hp2 HG01934.hp2 HG02015.hp2 others(42): Show |
intron_variant | MODIFIER | c.853-20683_853-2068 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853120 | ||||||
chr3:32853120 | CTTT | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0181 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.853-20684_853-2068 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853120 | ||||||
chr3:32853122 | T | C | 4 | a0001c0001t0004g0216 a0001c0001t0010g0235 a0001c0001t0010g0236 others(1): Show |
4 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-20696T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853122 | |||||||
chr3:32853123 | T | C | 2 | a0001c0001t0002g0317 a0001c0001t0002g0318 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853-20695T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853123 | |||||||
chr3:32853143 | G | T | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-20675G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853143 | |||||||
chr3:32853286 | T | C | 1 | a0001c0001t0030g0323 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.853-20532T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853286 | |||||||
chr3:32853338 | C | T | 106 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.853-20480C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853338 | |||||||
chr3:32853342 | C | T | 1 | a0001c0001t0031g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.853-20476C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853342 | |||||||
chr3:32853479 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.853-20339T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853479 | |||||||
chr3:32853707 | T | C | 1 | a0001c0001t0006g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.853-20111T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853707 | |||||||
chr3:32853965 | C | T | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-19853C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853965 | |||||||
chr3:32853991 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.853-19827G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853991 | |||||||
chr3:32854650 | A | G | 3 | a0001c0001t0004g0216 a0001c0001t0008g0271 a0001c0001t0008g0273 |
3 | HG00280.hp2 NA18964.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.853-19168A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32854650 | |||||||
chr3:32855093 | A | G | 1 | a0001c0002t0002g0166 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.853-18725A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855093 | |||||||
chr3:32855179 | G | A | 1 | a0001c0001t0044g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.853-18639G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855179 | |||||||
chr3:32855281 | C | T | 1 | a0001c0001t0012g0010 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.853-18537C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855281 | |||||||
chr3:32855294 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.853-18524G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855294 | |||||||
chr3:32855371 | G | C | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-18447G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855371 | |||||||
chr3:32855376 | A | G | 1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-18442A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855376 | |||||||
chr3:32855377 | G | A | 1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-18441G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855377 | |||||||
chr3:32855494 | G | A | 3 | a0001c0001t0003g0225 a0001c0001t0009g0224 a0001c0001t0009g0226 |
3 | HG01069.hp1 HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.853-18324G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855494 | |||||||
chr3:32855507 | ATGTCTCT others(4): Show |
A | 1 | a0001c0001t0001g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.853-18303_853-1829 others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32855507 | ||||||
chr3:32855533 | C | T | 1 | a0001c0001t0057g0270 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.853-18285C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855533 | |||||||
chr3:32855548 | A | G | 4 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0190 others(1): Show |
4 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-18270A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855548 | |||||||
chr3:32855747 | A | G | 1 | a0001c0001t0022g0165 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.853-18071A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855747 | |||||||
chr3:32855850 | G | A | 1 | a0001c0002t0002g0042 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.853-17968G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855850 | |||||||
chr3:32855901 | A | C | 6 | a0001c0001t0001g0140 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
6 | HG00735.hp2 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-17917A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855901 | |||||||
chr3:32855990 | T | TTTTA | 136 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(133): Show |
136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.853-17804_853-1780 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32855990 | ||||||
chr3:32855990 | T | TTTTATTT others(1): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0126 a0001c0001t0004g0157 others(4): Show |
7 | HG00621.hp1 HG02148.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.853-17808_853-1780 others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32855990 | ||||||
chr3:32855990 | T | TTTTATTT others(9): Show |
1 | a0001c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.853-17816_853-1780 others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32855990 | ||||||
chr3:32856178 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-17640C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856178 | |||||||
chr3:32856180 | G | A | 1 | a0001c0001t0016g0003 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-17638G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856180 | |||||||
chr3:32856365 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.853-17453C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856365 | |||||||
chr3:32856519 | A | G | 55 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0138 others(52): Show |
55 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.853-17299A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856519 | |||||||
chr3:32856713 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(219): Show |
224 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.853-17105G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856713 | |||||||
chr3:32856800 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-17018T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856800 | |||||||
chr3:32856854 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.853-16964C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856854 | |||||||
chr3:32856922 | C | T | 2 | a0001c0001t0007g0284 a0001c0003t0005g0285 |
2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.853-16896C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856922 | |||||||
chr3:32856944 | A | G | 1 | a0003c0006t0002g0193 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.853-16874A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856944 | |||||||
chr3:32857009 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0040g0254 |
2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.853-16809A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857009 | |||||||
chr3:32857044 | T | C | 2 | a0001c0001t0007g0284 a0001c0003t0005g0285 |
2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.853-16774T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857044 | |||||||
chr3:32857064 | G | C | 1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-16754G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857064 | |||||||
chr3:32857066 | C | G | 1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-16752C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857066 | |||||||
chr3:32857219 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.853-16599A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857219 | |||||||
chr3:32857383 | C | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0181 others(33): Show |
37 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.853-16435C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857383 | |||||||
chr3:32857405 | T | C | 1 | a0001c0001t0015g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.853-16413T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857405 | |||||||
chr3:32857428 | A | G | 1 | a0001c0002t0013g0264 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.853-16390A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857428 | |||||||
chr3:32857447 | C | T | 31 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(28): Show |
31 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.853-16371C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857447 | |||||||
chr3:32857496 | A | C | 1 | a0001c0001t0004g0157 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.853-16322A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857496 | |||||||
chr3:32857498 | G | A | 1 | a0001c0002t0024g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.853-16320G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857498 | |||||||
chr3:32857699 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0126 a0001c0001t0009g0148 others(2): Show |
5 | HG00323.hp1 HG00741.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-16119A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857699 | |||||||
chr3:32857791 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.853-16027C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857791 | |||||||
chr3:32857871 | T | C | 1 | a0001c0004t0011g0243 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.853-15947T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857871 | |||||||
chr3:32857917 | G | T | 1 | a0001c0001t0002g0296 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.853-15901G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857917 | |||||||
chr3:32857919 | C | T | 2 | a0001c0001t0003g0155 a0001c0001t0003g0200 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.853-15899C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857919 | |||||||
chr3:32857926 | G | A | 1 | a0001c0001t0018g0281 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853-15892G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857926 | |||||||
chr3:32858007 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.853-15811G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858007 | |||||||
chr3:32858018 | T | A | 1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-15800T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858018 | |||||||
chr3:32858265 | G | T | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-15553G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858265 | |||||||
chr3:32858320 | T | C | 1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-15498T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858320 | |||||||
chr3:32858321 | G | T | 1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-15497G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858321 | |||||||
chr3:32858322 | C | G | 1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-15496C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858322 | |||||||
chr3:32858333 | G | A | 1 | a0001c0002t0002g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.853-15485G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858333 | |||||||
chr3:32858347 | G | A | 5 | a0001c0001t0001g0110 a0001c0001t0002g0118 a0001c0001t0010g0235 others(2): Show |
5 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-15471G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858347 | |||||||
chr3:32858476 | C | T | 1 | a0001c0001t0039g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.853-15342C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858476 | |||||||
chr3:32858670 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.853-15148G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858670 | |||||||
chr3:32858709 | A | G | 3 | a0001c0001t0003g0217 a0001c0002t0002g0058 a0001c0002t0002g0059 |
3 | HG03710.hp1 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.853-15109A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858709 | |||||||
chr3:32858753 | T | C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0181 others(36): Show |
40 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.853-15065T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858753 | |||||||
chr3:32858756 | G | A | 1 | a0001c0001t0006g0167 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.853-15062G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858756 | |||||||
chr3:32858781 | G | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.853-15037G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858781 | |||||||
chr3:32858950 | T | C | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-14868T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858950 | |||||||
chr3:32859042 | T | G | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-14776T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859042 | |||||||
chr3:32859234 | C | T | 1 | a0001c0001t0006g0012 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.853-14584C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859234 | |||||||
chr3:32859251 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0003g0190 a0001c0001t0009g0240 |
3 | HG00741.hp1 HG01106.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.853-14567C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859251 | |||||||
chr3:32859359 | A | G | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-14459A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859359 | |||||||
chr3:32859411 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.853-14407C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859411 | |||||||
chr3:32859431 | G | GT | 27 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(24): Show |
27 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.853-14380dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32859431 | ||||||
chr3:32859626 | T | G | 13 | a0001c0001t0001g0231 a0001c0001t0001g0247 a0001c0001t0002g0233 others(10): Show |
13 | HG02258.hp1 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.853-14192T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859626 | |||||||
chr3:32859669 | G | T | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-14149G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859669 | |||||||
chr3:32859681 | G | C | 5 | a0001c0001t0001g0125 a0001c0001t0004g0048 a0001c0001t0006g0031 others(2): Show |
5 | HG00438.hp2 HG02523.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-14137G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859681 | |||||||
chr3:32859808 | C | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0110 a0001c0001t0001g0231 others(42): Show |
45 | HG00280.hp2 HG00544.hp2 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.853-14010C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859808 | |||||||
chr3:32859875 | G | A | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-13943G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859875 | |||||||
chr3:32859894 | G | A | 44 | a0001c0001t0001g0013 a0001c0001t0001g0110 a0001c0001t0001g0231 others(41): Show |
44 | HG00280.hp2 HG00544.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.853-13924G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859894 | |||||||
chr3:32860137 | TCCCTCCC others(5): Show |
T | 4 | a0001c0001t0020g0041 a0001c0001t0020g0049 a0001c0002t0002g0040 others(1): Show |
4 | NA18966.hp2 NA18968.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-13667_853-1365 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32860137 | ||||||
chr3:32860215 | A | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0315 a0001c0001t0037g0320 |
3 | HG02622.hp2 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.853-13603A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860215 | |||||||
chr3:32860369 | C | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.853-13449C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860369 | |||||||
chr3:32860435 | C | T | 3 | a0001c0001t0001g0302 a0001c0001t0002g0172 a0001c0003t0005g0027 |
3 | HG01934.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.853-13383C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860435 | |||||||
chr3:32860463 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0064 others(44): Show |
48 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(45): Show |
intron_variant | MODIFIER | c.853-13355C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860463 | |||||||
chr3:32860506 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.853-13312T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860506 | |||||||
chr3:32860530 | TCTC | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
220 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.853-13284_853-1328 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32860530 | ||||||
chr3:32860588 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.853-13230A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860588 | |||||||
chr3:32860671 | G | A | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-13147G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860671 | |||||||
chr3:32860801 | A | G | 1 | a0001c0001t0004g0157 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.853-13017A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860801 | |||||||
chr3:32860878 | A | T | 1 | a0001c0002t0002g0290 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.853-12940A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860878 | |||||||
chr3:32860888 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0002g0074 a0001c0001t0002g0077 others(1): Show |
4 | HG02970.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-12930C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860888 | |||||||
chr3:32860940 | C | T | 10 | a0001c0001t0001g0231 a0001c0001t0001g0247 a0001c0001t0002g0233 others(7): Show |
10 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-12878C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860940 | |||||||
chr3:32860982 | C | T | 1 | a0001c0002t0002g0322 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.853-12836C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860982 | |||||||
chr3:32861067 | CTG | C | 3 | a0001c0001t0001g0013 a0001c0001t0018g0281 a0001c0008t0007g0025 |
3 | HG01884.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.853-12750_853-1274 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861067 | |||||||
chr3:32861080 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.853-12738C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861080 | |||||||
chr3:32861096 | T | A | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-12722T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861096 | |||||||
chr3:32861139 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.853-12679T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861139 | |||||||
chr3:32861224 | C | A | 1 | a0001c0001t0020g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.853-12594C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861224 | |||||||
chr3:32861297 | C | T | 1 | a0001c0003t0005g0321 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.853-12521C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861297 | |||||||
chr3:32861458 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0017g0278 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.853-12360C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861458 | |||||||
chr3:32861516 | CCG | C | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-12301_853-1230 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861516 | |||||||
chr3:32861525 | A | C | 3 | a0001c0001t0001g0302 a0001c0001t0002g0172 a0001c0003t0005g0027 |
3 | HG01934.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.853-12293A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861525 | |||||||
chr3:32861525 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(257): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.853-12293A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861525 | |||||||
chr3:32861610 | C | T | 1 | a0001c0002t0023g0046 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.853-12208C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861610 | |||||||
chr3:32861639 | C | G | 2 | a0001c0001t0002g0317 a0001c0001t0002g0318 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853-12179C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861639 | |||||||
chr3:32861833 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.853-11985C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861833 | |||||||
chr3:32861913 | C | T | 3 | a0001c0001t0007g0284 a0001c0003t0005g0097 a0001c0003t0005g0300 |
3 | HG02559.hp1 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.853-11905C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861913 | |||||||
chr3:32861972 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.853-11846C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861972 | |||||||
chr3:32862231 | C | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
220 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.853-11587C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862231 | |||||||
chr3:32862335 | C | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0110 a0001c0001t0001g0302 others(4): Show |
7 | HG01884.hp2 HG01934.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.853-11483C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862335 | |||||||
chr3:32862715 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
76 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.853-11103G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862715 | |||||||
chr3:32862918 | C | G | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-10900C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862918 | |||||||
chr3:32862918 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
76 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.853-10900C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862918 | |||||||
chr3:32862925 | T | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.853-10893T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862925 | |||||||
chr3:32863023 | G | A | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-10795G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863023 | |||||||
chr3:32863023 | G | T | 4 | a0001c0001t0003g0225 a0001c0001t0009g0224 a0001c0001t0009g0226 others(1): Show |
4 | HG01069.hp1 HG01123.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-10795G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863023 | |||||||
chr3:32863058 | A | T | 1 | a0001c0002t0002g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.853-10760A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863058 | |||||||
chr3:32863067 | T | TTATTAGG others(3): Show |
1 | a0001c0002t0002g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-10749_853-1074 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863067 | ||||||
chr3:32863160 | C | G | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-10658C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863160 | |||||||
chr3:32863194 | C | CTTT | 3 | a0001c0001t0001g0076 a0001c0001t0002g0074 a0001c0001t0002g0232 |
3 | HG02970.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.853-10624_853-1062 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863194 | |||||||
chr3:32863195 | C | CT | 72 | a0001c0001t0001g0054 a0001c0001t0001g0110 a0001c0001t0001g0138 others(69): Show |
73 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.853-10597dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | ||||||
chr3:32863195 | C | CTT | 18 | a0001c0001t0001g0125 a0001c0001t0001g0214 a0001c0001t0002g0313 others(15): Show |
18 | HG00280.hp2 HG01109.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.853-10598_853-1059 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | ||||||
chr3:32863195 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0002g0074 a0001c0001t0002g0077 others(1): Show |
4 | HG02970.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-10623C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863195 | |||||||
chr3:32863195 | CT | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(117): Show |
122 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.853-10597delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | ||||||
chr3:32863195 | CTT | C | 58 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0030 others(55): Show |
59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.853-10598_853-1059 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | ||||||
chr3:32863195 | CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0002g0208 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.853-10609_853-1059 others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | ||||||
chr3:32863397 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-10421T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863397 | |||||||
chr3:32863405 | G | A | 1 | a0001c0001t0021g0174 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.853-10413G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863405 | |||||||
chr3:32863425 | C | G | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-10393C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863425 | |||||||
chr3:32863527 | C | T | 1 | a0001c0001t0008g0266 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.853-10291C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863527 | |||||||
chr3:32863528 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0194 a0001c0001t0001g0196 others(6): Show |
9 | HG00558.hp2 HG02074.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-10290G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863528 | |||||||
chr3:32863586 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-10232A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863586 | |||||||
chr3:32863943 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0082 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.853-9875A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863943 | |||||||
chr3:32863984 | T | A | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-9834T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863984 | |||||||
chr3:32863985 | C | A | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-9833C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863985 | |||||||
chr3:32864013 | G | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(302): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.853-9805G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864013 | |||||||
chr3:32864030 | C | T | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-9788C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864030 | |||||||
chr3:32864120 | G | A | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-9698G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864120 | |||||||
chr3:32864312 | T | G | 4 | a0001c0001t0001g0013 a0001c0001t0018g0281 a0001c0003t0005g0027 others(1): Show |
4 | HG01884.hp2 HG01934.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-9506T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864312 | |||||||
chr3:32864314 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-9504G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864314 | |||||||
chr3:32864608 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.853-9210G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864608 | |||||||
chr3:32864817 | A | G | 10 | a0001c0001t0001g0231 a0001c0001t0001g0247 a0001c0001t0002g0233 others(7): Show |
10 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-9001A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864817 | |||||||
chr3:32864842 | AGTGGTGT others(8): Show |
A | 1 | a0001c0003t0005g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.853-8972_853-8958d others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864842 | ||||||
chr3:32864845 | G | GGT | 13 | a0001c0001t0001g0140 a0001c0001t0001g0163 a0001c0001t0001g0164 others(10): Show |
13 | HG00597.hp2 HG00621.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-8926_853-8925d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | G | GGTGT | 4 | a0001c0001t0002g0306 a0001c0001t0007g0310 a0001c0002t0002g0136 others(1): Show |
4 | HG00423.hp2 HG02074.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-8928_853-8925d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | G | GGTGTGT | 4 | a0001c0002t0002g0287 a0001c0002t0002g0291 a0001c0002t0002g0292 others(1): Show |
4 | NA18945.hp2 NA18973.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-8930_853-8925d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGT | G | 31 | a0001c0001t0001g0108 a0001c0001t0001g0116 a0001c0001t0001g0173 others(28): Show |
31 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.853-8926_853-8925d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGT | G | 24 | a0001c0001t0001g0028 a0001c0001t0001g0187 a0001c0001t0001g0214 others(21): Show |
24 | HG00544.hp1 HG01993.hp1 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.853-8928_853-8925d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGTGT | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(32): Show |
36 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.853-8930_853-8925d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGTGTG others(1): Show |
G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0194 others(5): Show |
8 | HG00544.hp2 HG01081.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-8932_853-8925d others(10): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGTGTG others(3): Show |
G | 9 | a0001c0001t0001g0138 a0001c0001t0003g0056 a0001c0001t0004g0048 others(6): Show |
9 | HG00280.hp1 HG00438.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-8934_853-8925d others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGTGTG others(5): Show |
G | 57 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0054 others(54): Show |
57 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.853-8936_853-8925d others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGTGTG others(7): Show |
G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.853-8938_853-8925d others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGTGTG others(9): Show |
G | 10 | a0001c0001t0002g0118 a0001c0001t0002g0317 a0001c0001t0002g0318 others(7): Show |
10 | HG01109.hp2 HG02015.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-8940_853-8925d others(18): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGTGTG others(11): Show |
G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0231 a0001c0001t0001g0247 others(5): Show |
8 | HG01081.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.853-8942_853-8925d others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGTGTG others(13): Show |
G | 8 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 others(5): Show |
8 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-8944_853-8925d others(22): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864845 | GGTGTGTG others(17): Show |
G | 4 | a0001c0001t0015g0072 a0001c0001t0015g0073 a0001c0003t0005g0068 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-8948_853-8925d others(26): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | ||||||
chr3:32864892 | G | C | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-8926G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864892 | |||||||
chr3:32865096 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.853-8722G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865096 | |||||||
chr3:32865386 | C | T | 53 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0125 others(50): Show |
53 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.853-8432C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865386 | |||||||
chr3:32865410 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-8408T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865410 | |||||||
chr3:32865419 | G | A | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-8399G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865419 | |||||||
chr3:32865523 | C | T | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-8295C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865523 | |||||||
chr3:32865530 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0087 others(6): Show |
9 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.853-8288G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865530 | |||||||
chr3:32865601 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.853-8217A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865601 | |||||||
chr3:32865674 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.853-8144G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865674 | |||||||
chr3:32865737 | G | A | 13 | a0001c0001t0001g0231 a0001c0001t0001g0247 a0001c0001t0002g0233 others(10): Show |
13 | HG02258.hp1 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.853-8081G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865737 | |||||||
chr3:32865790 | CG | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0028 others(19): Show |
23 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.853-8026delG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865790 | ||||||
chr3:32865791 | G | GC | 13 | a0001c0001t0002g0318 a0001c0001t0004g0168 a0001c0001t0004g0294 others(10): Show |
13 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-8027_853-8026i others(3): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | |||||||
chr3:32865791 | G | GCC | 9 | a0001c0001t0001g0126 a0001c0001t0003g0217 a0001c0002t0002g0136 others(6): Show |
9 | HG02074.hp1 HG02148.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.853-8027_853-8026i others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | |||||||
chr3:32865791 | GGC | G | 31 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0158 others(28): Show |
31 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.853-8026_853-8025d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | |||||||
chr3:32865791 | GGCC | G | 31 | a0001c0001t0001g0030 a0001c0001t0001g0140 a0001c0001t0001g0164 others(28): Show |
31 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.853-8026_853-8024d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | |||||||
chr3:32865791 | GGCCC | G | 18 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0003g0155 others(15): Show |
19 | HG00099.hp1 HG01069.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.853-8026_853-8023d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | |||||||
chr3:32865791 | GGCCCCCC others(3): Show |
G | 5 | a0001c0001t0001g0076 a0001c0001t0002g0074 a0001c0001t0002g0077 others(2): Show |
5 | HG02970.hp1 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-8026_853-8017d others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | |||||||
chr3:32865791 | GGCCCCCC others(4): Show |
G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
80 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.853-8026_853-8016d others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | |||||||
chr3:32865792 | G | C | 41 | a0001c0001t0001g0108 a0001c0001t0001g0126 a0001c0001t0001g0211 others(38): Show |
41 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.853-8026G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865792 | |||||||
chr3:32865792 | GCC | G | 41 | a0001c0001t0001g0054 a0001c0001t0001g0125 a0001c0001t0001g0138 others(38): Show |
41 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-8012_853-8011d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865792 | ||||||
chr3:32865796 | C | A | 2 | a0001c0001t0003g0200 a0001c0002t0002g0253 |
2 | HG01192.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.853-8022C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865796 | |||||||
chr3:32865797 | C | A | 5 | a0001c0001t0003g0155 a0001c0001t0014g0246 a0001c0001t0014g0250 others(2): Show |
5 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-8021C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865797 | |||||||
chr3:32865799 | C | G | 1 | a0001c0001t0003g0201 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.853-8019C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865799 | |||||||
chr3:32865803 | C | A | 1 | a0001c0002t0023g0046 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.853-8015C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865803 | |||||||
chr3:32865808 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-8010G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865808 | |||||||
chr3:32865813 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-8005A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865813 | |||||||
chr3:32865815 | C | CCCACCTT others(20): Show |
1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-8003_853-8002i others(29): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865815 | |||||||
chr3:32865815 | C | CT | 8 | a0001c0001t0001g0249 a0001c0001t0003g0225 a0001c0001t0009g0224 others(5): Show |
8 | HG01081.hp1 HG01123.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.853-7975dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865815 | C | CTT | 36 | a0001c0001t0001g0054 a0001c0001t0001g0125 a0001c0001t0001g0218 others(33): Show |
36 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-7976_853-7975d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865815 | C | CTTT | 14 | a0001c0001t0001g0035 a0001c0001t0001g0138 a0001c0001t0003g0056 others(11): Show |
14 | HG00280.hp1 HG01952.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.853-7977_853-7975d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865815 | CTT | C | 16 | a0001c0001t0001g0102 a0001c0001t0001g0221 a0001c0001t0001g0222 others(13): Show |
16 | HG01256.hp1 HG01934.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.853-7976_853-7975d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865815 | CTTT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(93): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.853-7977_853-7975d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865815 | CTTTT | C | 91 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0028 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.853-7978_853-7975d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865815 | CTTTTT | C | 6 | a0001c0001t0001g0126 a0001c0001t0007g0121 a0001c0001t0008g0275 others(3): Show |
6 | HG02132.hp1 HG02148.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-7979_853-7975d others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865815 | CTTTTTT | C | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-7980_853-7975d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865815 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0135 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.853-7985_853-7975d others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865815 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0302 a0001c0001t0002g0172 a0001c0001t0002g0314 |
3 | HG02886.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.853-7986_853-7975d others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | ||||||
chr3:32865843 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.853-7975T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865843 | |||||||
chr3:32865936 | C | T | 28 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(25): Show |
28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-7882C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865936 | |||||||
chr3:32865967 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0018g0281 a0001c0003t0005g0027 others(1): Show |
4 | HG01884.hp2 HG01934.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7851C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865967 | |||||||
chr3:32866133 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
81 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.853-7685C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866133 | |||||||
chr3:32866163 | G | GT | 36 | a0001c0001t0001g0181 a0001c0001t0001g0302 a0001c0001t0002g0077 others(33): Show |
36 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(33): Show |
intron_variant | MODIFIER | c.853-7645dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32866163 | ||||||
chr3:32866165 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-7653T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866165 | |||||||
chr3:32866327 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-7491C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866327 | |||||||
chr3:32866374 | T | A | 10 | a0001c0001t0001g0231 a0001c0001t0001g0247 a0001c0001t0002g0233 others(7): Show |
10 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-7444T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866374 | |||||||
chr3:32866507 | G | A | 10 | a0001c0001t0001g0125 a0001c0001t0001g0218 a0001c0001t0001g0219 others(7): Show |
10 | HG00438.hp2 HG01358.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-7311G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866507 | |||||||
chr3:32866518 | C | T | 2 | a0001c0002t0002g0042 a0001c0002t0046g0065 |
2 | HG01978.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.853-7300C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866518 | |||||||
chr3:32866701 | A | G | 3 | a0001c0001t0001g0302 a0001c0001t0002g0172 a0001c0001t0051g0096 |
3 | HG02896.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.853-7117A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866701 | |||||||
chr3:32866744 | G | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-7074G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866744 | |||||||
chr3:32866941 | AC | A | 3 | a0001c0001t0001g0229 a0001c0001t0006g0228 a0001c0001t0033g0179 |
3 | HG02056.hp1 HG02129.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.853-6876delC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866941 | |||||||
chr3:32867001 | T | A | 3 | a0001c0001t0001g0302 a0001c0001t0002g0172 a0001c0001t0051g0096 |
3 | HG02896.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.853-6817T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867001 | |||||||
chr3:32867041 | C | T | 3 | a0001c0001t0003g0225 a0001c0001t0009g0224 a0001c0001t0009g0226 |
3 | HG01069.hp1 HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.853-6777C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867041 | |||||||
chr3:32867072 | TC | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-6745delC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867072 | |||||||
chr3:32867140 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): Show |
152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.853-6678C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867140 | |||||||
chr3:32867171 | A | AC | 16 | a0001c0001t0004g0038 a0001c0001t0004g0135 a0001c0001t0004g0143 others(13): Show |
16 | HG00544.hp2 HG00597.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.853-6641dupC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32867171 | ||||||
chr3:32867181 | C | T | 1 | a0001c0002t0002g0322 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.853-6637C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867181 | |||||||
chr3:32867188 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(316): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.853-6630C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867188 | |||||||
chr3:32867190 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0002g0067 a0001c0001t0018g0099 others(2): Show |
5 | HG01934.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-6628T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867190 | |||||||
chr3:32867344 | A | G | 1 | a0001c0008t0007g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853-6474A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867344 | |||||||
chr3:32867511 | G | A | 4 | a0001c0001t0002g0317 a0001c0001t0002g0318 a0001c0001t0018g0099 others(1): Show |
4 | HG02559.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-6307G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867511 | |||||||
chr3:32867572 | C | A | 32 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(29): Show |
32 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.853-6246C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867572 | |||||||
chr3:32867644 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.853-6174A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867644 | |||||||
chr3:32867708 | C | A | 1 | a0001c0001t0008g0271 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.853-6110C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867708 | |||||||
chr3:32867717 | AT | A | 36 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-6094delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32867717 | ||||||
chr3:32867719 | T | C | 36 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-6099T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867719 | |||||||
chr3:32867763 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.853-6055A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867763 | |||||||
chr3:32867778 | C | G | 36 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-6040C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867778 | |||||||
chr3:32867834 | T | G | 1 | a0001c0001t0002g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.853-5984T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867834 | |||||||
chr3:32867931 | T | C | 3 | a0001c0001t0014g0246 a0001c0001t0014g0250 a0001c0001t0014g0280 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.853-5887T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867931 | |||||||
chr3:32868028 | T | G | 1 | a0001c0001t0016g0003 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-5790T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868028 | |||||||
chr3:32868253 | CT | C | 37 | a0001c0001t0001g0230 a0001c0001t0003g0045 a0001c0001t0004g0036 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.853-5563delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868253 | ||||||
chr3:32868450 | A | G | 1 | a0001c0001t0042g0107 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.853-5368A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868450 | |||||||
chr3:32868516 | A | G | 3 | a0001c0001t0001g0054 a0001c0002t0023g0046 a0001c0002t0023g0053 |
3 | NA18975.hp2 NA18981.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.853-5302A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868516 | |||||||
chr3:32868636 | C | CT | 5 | a0001c0001t0002g0172 a0001c0001t0016g0003 a0001c0001t0051g0096 others(2): Show |
6 | HG00609.hp2 HG01884.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-5170dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868636 | ||||||
chr3:32868661 | GGAGACAA others(6): Show |
G | 41 | a0001c0001t0001g0230 a0001c0001t0003g0045 a0001c0001t0004g0036 others(38): Show |
41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-5150_853-5138d others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868661 | ||||||
chr3:32868686 | G | GT | 34 | a0001c0001t0001g0006 a0001c0001t0001g0249 a0001c0001t0003g0045 others(31): Show |
34 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.853-5118dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868686 | ||||||
chr3:32868686 | G | GTT | 8 | a0001c0001t0001g0230 a0001c0001t0004g0061 a0001c0001t0004g0216 others(5): Show |
8 | HG00280.hp2 HG02040.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.853-5119_853-5118d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868686 | ||||||
chr3:32868688 | T | A | 1 | a0001c0001t0007g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.853-5130T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868688 | |||||||
chr3:32868699 | T | A | 3 | a0001c0001t0007g0310 a0001c0003t0005g0024 a0001c0003t0005g0027 |
3 | HG01934.hp2 HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.853-5119T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868699 | |||||||
chr3:32868700 | T | A | 47 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0075 others(44): Show |
48 | HG00323.hp1 HG00639.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.853-5118T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868700 | |||||||
chr3:32868700 | TA | T | 5 | a0001c0001t0001g0302 a0001c0001t0002g0118 a0001c0001t0015g0244 others(2): Show |
5 | HG02647.hp2 HG02896.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-5112delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868700 | ||||||
chr3:32868701 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-5117A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868701 | |||||||
chr3:32868701 | A | T | 57 | a0001c0001t0001g0076 a0001c0001t0001g0125 a0001c0001t0001g0140 others(54): Show |
57 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.853-5117A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868701 | |||||||
chr3:32868702 | A | T | 4 | a0001c0001t0004g0135 a0001c0001t0004g0216 a0001c0001t0008g0263 others(1): Show |
4 | HG00280.hp2 HG02074.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-5116A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868702 | |||||||
chr3:32868761 | TA | T | 3 | a0001c0001t0015g0244 a0001c0001t0045g0071 a0001c0002t0002g0070 |
3 | HG02647.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.853-5052delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868761 | ||||||
chr3:32868789 | T | C | 41 | a0001c0001t0001g0230 a0001c0001t0003g0045 a0001c0001t0004g0036 others(38): Show |
41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-5029T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868789 | |||||||
chr3:32868829 | G | A | 2 | a0001c0001t0016g0003 a0001c0008t0007g0025 |
3 | HG01884.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-4989G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868829 | |||||||
chr3:32868968 | A | G | 41 | a0001c0001t0001g0230 a0001c0001t0003g0045 a0001c0001t0004g0036 others(38): Show |
41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-4850A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868968 | |||||||
chr3:32869050 | T | C | 15 | a0001c0001t0001g0076 a0001c0001t0002g0067 a0001c0001t0002g0074 others(12): Show |
15 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.853-4768T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869050 | |||||||
chr3:32869094 | G | C | 3 | a0001c0001t0022g0156 a0001c0001t0022g0165 a0002c0005t0001g0159 |
3 | HG00438.hp1 NA18966.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.853-4724G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869094 | |||||||
chr3:32869294 | C | G | 4 | a0001c0001t0020g0041 a0001c0001t0020g0049 a0001c0001t0055g0268 others(1): Show |
4 | NA18966.hp2 NA18992.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-4524C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869294 | |||||||
chr3:32869332 | C | G | 3 | a0001c0001t0006g0132 a0001c0001t0006g0212 a0001c0002t0002g0129 |
3 | HG01993.hp1 HG02132.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.853-4486C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869332 | |||||||
chr3:32869397 | G | A | 36 | a0001c0001t0001g0230 a0001c0001t0003g0045 a0001c0001t0004g0036 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-4421G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869397 | |||||||
chr3:32869424 | T | A | 1 | a0001c0002t0002g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.853-4394T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869424 | |||||||
chr3:32869799 | G | A | 1 | a0001c0001t0027g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.853-4019G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869799 | |||||||
chr3:32869864 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-3954G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869864 | |||||||
chr3:32869892 | T | C | 1 | a0001c0002t0002g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.853-3926T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869892 | |||||||
chr3:32869906 | C | T | 8 | a0001c0001t0001g0076 a0001c0001t0002g0067 a0001c0001t0002g0074 others(5): Show |
8 | HG02970.hp1 HG03098.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-3912C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869906 | |||||||
chr3:32869912 | G | A | 6 | a0001c0001t0007g0004 a0001c0001t0007g0069 a0001c0001t0007g0308 others(3): Show |
7 | HG00639.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.853-3906G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869912 | |||||||
chr3:32869919 | A | T | 6 | a0001c0001t0007g0004 a0001c0001t0007g0069 a0001c0001t0007g0308 others(3): Show |
7 | HG00639.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.853-3899A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869919 | |||||||
chr3:32870036 | G | T | 3 | a0001c0001t0015g0244 a0001c0001t0045g0071 a0001c0002t0002g0070 |
3 | HG02647.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.853-3782G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870036 | |||||||
chr3:32870168 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.853-3650A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870168 | |||||||
chr3:32870432 | A | G | 1 | a0001c0001t0004g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.853-3386A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870432 | |||||||
chr3:32870528 | G | C | 1 | a0001c0001t0053g0269 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.853-3290G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870528 | |||||||
chr3:32870836 | C | T | 1 | a0001c0001t0016g0003 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-2982C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870836 | |||||||
chr3:32870896 | T | G | 1 | a0001c0001t0016g0003 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-2922T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870896 | |||||||
chr3:32870916 | A | G | 201 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0075 others(198): Show |
203 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.853-2902A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870916 | |||||||
chr3:32870968 | A | AT | 87 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0075 others(84): Show |
87 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.853-2833dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32870968 | ||||||
chr3:32870968 | A | ATT | 8 | a0001c0001t0007g0004 a0001c0001t0007g0308 a0001c0001t0007g0310 others(5): Show |
9 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-2834_853-2833d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32870968 | ||||||
chr3:32870968 | AT | A | 11 | a0001c0001t0001g0113 a0001c0001t0001g0158 a0001c0001t0001g0162 others(8): Show |
11 | HG01167.hp1 HG01358.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-2833delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32870968 | ||||||
chr3:32871107 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.853-2711G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871107 | |||||||
chr3:32871155 | A | G | 2 | a0001c0001t0007g0119 a0001c0001t0007g0121 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.853-2663A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871155 | |||||||
chr3:32871159 | A | G | 1 | a0001c0001t0008g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.853-2659A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871159 | |||||||
chr3:32871258 | C | T | 48 | a0001c0001t0001g0230 a0001c0001t0001g0249 a0001c0001t0003g0045 others(45): Show |
49 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.853-2560C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871258 | |||||||
chr3:32871292 | C | G | 1 | a0001c0001t0004g0168 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.853-2526C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871292 | |||||||
chr3:32871313 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.853-2505T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871313 | |||||||
chr3:32871345 | A | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG00735.hp2 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-2473A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871345 | |||||||
chr3:32871355 | C | A | 2 | a0001c0001t0014g0246 a0001c0001t0014g0250 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.853-2463C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871355 | |||||||
chr3:32871422 | C | T | 1 | a0001c0003t0005g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.853-2396C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871422 | |||||||
chr3:32871514 | C | T | 1 | a0001c0001t0007g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.853-2304C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871514 | |||||||
chr3:32871588 | C | G | 2 | a0001c0001t0012g0169 a0001c0007t0012g0133 |
2 | HG00323.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.853-2230C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871588 | |||||||
chr3:32871601 | T | C | 190 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0075 others(187): Show |
192 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.853-2217T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871601 | |||||||
chr3:32871910 | A | G | 1 | a0001c0001t0026g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.853-1908A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871910 | |||||||
chr3:32872002 | G | A | 1 | a0001c0001t0031g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.853-1816G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872002 | |||||||
chr3:32872096 | G | A | 1 | a0001c0001t0057g0270 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.853-1722G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872096 | |||||||
chr3:32872122 | C | T | 48 | a0001c0001t0001g0230 a0001c0001t0001g0249 a0001c0001t0003g0045 others(45): Show |
49 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.853-1696C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872122 | |||||||
chr3:32872160 | CAAAT | C | 10 | a0001c0001t0012g0169 a0001c0002t0002g0015 a0001c0002t0002g0016 others(7): Show |
10 | HG01109.hp2 HG01167.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-1654_853-1651d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32872160 | ||||||
chr3:32872212 | A | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(316): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.853-1606A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872212 | |||||||
chr3:32872246 | G | C | 41 | a0001c0001t0001g0230 a0001c0001t0003g0045 a0001c0001t0004g0036 others(38): Show |
41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-1572G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872246 | |||||||
chr3:32872266 | G | A | 3 | a0001c0001t0016g0003 a0001c0001t0051g0096 a0001c0008t0007g0025 |
4 | HG01884.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-1552G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872266 | |||||||
chr3:32872404 | T | C | 1 | a0001c0001t0002g0317 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.853-1414T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872404 | |||||||
chr3:32872518 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.853-1300T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872518 | |||||||
chr3:32872820 | G | C | 1 | a0001c0001t0039g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.853-998G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872820 | |||||||
chr3:32872914 | C | G | 1 | a0001c0003t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.853-904C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872914 | |||||||
chr3:32873056 | T | TCTCCCTC others(9): Show |
1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.853-759_853-758ins others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873056 | ||||||
chr3:32873056 | TCTCTCTT others(5): Show |
T | 2 | a0001c0001t0001g0247 a0001c0001t0038g0316 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.853-758_853-747del others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873056 | ||||||
chr3:32873059 | CTCTT | C | 3 | a0001c0001t0018g0099 a0001c0001t0018g0281 a0001c0002t0023g0053 |
3 | HG02559.hp2 NA18906.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.853-758_853-755del others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873059 | |||||||
chr3:32873060 | T | C | 2 | a0001c0001t0001g0302 a0001c0001t0002g0118 |
2 | HG02896.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.853-758T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873060 | |||||||
chr3:32873060 | T | TCTCCCTC others(5): Show |
1 | a0001c0001t0001g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.853-756_853-755ins others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873060 | ||||||
chr3:32873060 | TCTTC | T | 4 | a0001c0001t0004g0036 a0001c0001t0004g0168 a0001c0002t0002g0151 others(1): Show |
4 | NA18992.hp1 NA19003.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-755_853-752del others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873060 | ||||||
chr3:32873060 | TCTTCCTC others(1): Show |
T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0139 a0001c0001t0001g0141 others(30): Show |
33 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.853-755_853-748del others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873060 | ||||||
chr3:32873060 | TCTTCCTC others(9): Show |
T | 1 | a0001c0001t0014g0280 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.853-755_853-740del others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873060 | ||||||
chr3:32873063 | T | C | 10 | a0001c0001t0001g0076 a0001c0001t0001g0302 a0001c0001t0002g0118 others(7): Show |
10 | HG01256.hp2 HG01258.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-755T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873063 | |||||||
chr3:32873063 | T | TCCTC | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.853-724_853-721dup others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873063 | T | TCCTCCCT others(1): Show |
15 | a0001c0001t0001g0197 a0001c0001t0006g0132 a0001c0001t0006g0167 others(12): Show |
15 | HG00140.hp1 HG00558.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.853-728_853-721dup others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873063 | T | TCCTCCCT others(5): Show |
21 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0103 others(18): Show |
22 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-732_853-721dup others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873063 | T | TCCTCCCT others(9): Show |
2 | a0001c0001t0009g0090 a0001c0001t0009g0185 |
2 | HG03239.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.853-736_853-721dup others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873063 | T | TCCTCCCT others(13): Show |
4 | a0001c0001t0001g0054 a0001c0001t0016g0003 a0001c0001t0045g0071 others(1): Show |
5 | HG02647.hp2 HG03139.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-740_853-721dup others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873063 | T | TCCTCCCT others(17): Show |
5 | a0001c0001t0002g0077 a0001c0001t0002g0232 a0001c0001t0007g0284 others(2): Show |
5 | HG02559.hp1 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-744_853-721dup others(24): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873063 | T | TCCTCCCT others(21): Show |
1 | a0001c0001t0002g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.853-748_853-721dup others(28): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873063 | TCCTC | T | 46 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0123 others(43): Show |
46 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.853-724_853-721del others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873063 | TCCTCCCT others(1): Show |
T | 6 | a0001c0001t0001g0203 a0001c0001t0001g0249 a0001c0002t0002g0062 others(3): Show |
6 | HG01081.hp1 HG01109.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-728_853-721del others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873063 | TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0002g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.853-732_853-721del others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | ||||||
chr3:32873116 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0002g0067 a0001c0001t0002g0074 others(7): Show |
10 | HG02559.hp1 HG02809.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-702G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873116 | |||||||
chr3:32873161 | C | G | 1 | a0001c0001t0002g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.853-657C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873161 | |||||||
chr3:32873362 | A | G | 1 | a0001c0001t0026g0319 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.853-456A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873362 | |||||||
chr3:32873589 | C | T | 9 | a0001c0001t0002g0067 a0001c0001t0002g0074 a0001c0001t0002g0077 others(6): Show |
9 | HG02559.hp1 HG02809.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.853-229C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873589 | |||||||
chr3:32873605 | T | G | 8 | a0001c0001t0003g0225 a0001c0001t0009g0090 a0001c0001t0009g0115 others(5): Show |
8 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-213T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873605 | |||||||
chr3:32873722 | C | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(316): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.853-96C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873722 | |||||||
chr3:32873726 | C | T | 1 | a0001c0001t0007g0069 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.853-92C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873726 | |||||||
chr3:32873804 | T | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0125 others(7): Show |
10 | HG00544.hp2 HG00621.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-14T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873804 | |||||||
chr3:32873811 | T | C | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
splice_region_variant&intron_variant | LOW | c.853-7T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873811 | |||||||
chr3:32874150 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1020+165C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874150 | |||||||
chr3:32874165 | G | C | 8 | a0001c0001t0003g0225 a0001c0001t0009g0090 a0001c0001t0009g0115 others(5): Show |
8 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+180G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874165 | |||||||
chr3:32874183 | G | C | 42 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(39): Show |
42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+198G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874183 | |||||||
chr3:32874320 | C | CTTA | 9 | a0001c0001t0004g0036 a0001c0001t0004g0051 a0001c0001t0004g0057 others(6): Show |
9 | NA18945.hp1 NA18966.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020+339_1020+341d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874320 | ||||||
chr3:32874320 | C | CTTATTA | 27 | a0001c0001t0003g0045 a0001c0001t0004g0037 a0001c0001t0004g0038 others(24): Show |
27 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.1020+336_1020+341d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874320 | ||||||
chr3:32874320 | CTTA | C | 16 | a0001c0001t0001g0076 a0001c0001t0001g0100 a0001c0001t0001g0231 others(13): Show |
16 | HG00323.hp1 HG01167.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020+339_1020+341d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874320 | ||||||
chr3:32874321 | TTATTAC | T | 16 | a0001c0001t0015g0072 a0001c0001t0015g0073 a0001c0002t0002g0111 others(13): Show |
16 | HG01109.hp1 HG01891.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020+339_1020+344d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874321 | ||||||
chr3:32874324 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0247 a0001c0001t0001g0249 others(6): Show |
9 | HG01081.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1020+339T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874324 | |||||||
chr3:32874324 | T | TTAC | 4 | a0001c0001t0001g0125 a0001c0001t0001g0181 a0001c0003t0005g0097 others(1): Show |
4 | HG02559.hp1 HG02809.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020+382_1020+384d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | ||||||
chr3:32874324 | T | TTATTAC | 3 | a0001c0001t0004g0142 a0001c0001t0004g0157 a0001c0001t0004g0213 |
3 | NA18953.hp1 NA18994.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1020+341_1020+342i others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | ||||||
chr3:32874324 | T | TTATTATT others(2): Show |
3 | a0001c0001t0006g0032 a0001c0001t0006g0043 a0001c0001t0008g0276 |
3 | NA19007.hp2 NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1020+341_1020+342i others(11): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | ||||||
chr3:32874324 | TTAC | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1020+382_1020+384d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | ||||||
chr3:32874324 | TTACTAC | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0003g0225 others(45): Show |
48 | HG00544.hp1 HG00609.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1020+379_1020+384d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | ||||||
chr3:32874324 | TTACTACT others(2): Show |
T | 4 | a0001c0001t0015g0244 a0001c0001t0016g0003 a0001c0001t0045g0071 others(1): Show |
5 | HG02647.hp2 HG03139.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+376_1020+384d others(11): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | ||||||
chr3:32874324 | TTACTACT others(8): Show |
T | 1 | a0001c0001t0001g0007 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1020+370_1020+384d others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | ||||||
chr3:32874327 | C | T | 12 | a0001c0001t0004g0036 a0001c0001t0004g0051 a0001c0001t0004g0057 others(9): Show |
12 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1020+342C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874327 | |||||||
chr3:32874330 | C | T | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1020+345C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874330 | |||||||
chr3:32874352 | TACTACTA others(11): Show |
T | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1020+370_1020+387d others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874352 | ||||||
chr3:32874358 | TACTACTA others(5): Show |
T | 1 | a0001c0003t0005g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1020+376_1020+387d others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874358 | ||||||
chr3:32874364 | T | A | 33 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0100 others(30): Show |
33 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1020+379T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874364 | |||||||
chr3:32874367 | T | A | 109 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0076 others(106): Show |
109 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1020+382T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874367 | |||||||
chr3:32874367 | T | TACA | 12 | a0001c0001t0003g0112 a0001c0001t0003g0171 a0001c0001t0003g0180 others(9): Show |
13 | HG01123.hp1 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1020+386_1020+388d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874367 | ||||||
chr3:32874370 | A | T | 42 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(39): Show |
42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+385A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874370 | |||||||
chr3:32874559 | G | C | 1 | a0001c0001t0003g0190 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1020+574G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874559 | |||||||
chr3:32874663 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1020+678C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874663 | |||||||
chr3:32874667 | C | A | 42 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(39): Show |
42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+682C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874667 | |||||||
chr3:32874672 | A | G | 42 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(39): Show |
42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+687A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874672 | |||||||
chr3:32874841 | A | T | 2 | a0001c0002t0002g0124 a0001c0002t0002g0146 |
2 | HG00423.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1020+856A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874841 | |||||||
chr3:32874907 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0017g0258 |
3 | HG02080.hp1 NA19009.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1020+922G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874907 | |||||||
chr3:32874966 | G | A | 2 | a0001c0001t0003g0155 a0001c0001t0003g0200 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1020+981G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874966 | |||||||
chr3:32875035 | G | A | 29 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0055 others(26): Show |
29 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1020+1050G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875035 | |||||||
chr3:32875225 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1020+1240C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875225 | |||||||
chr3:32875229 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1020+1244A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875229 | |||||||
chr3:32875476 | A | G | 45 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(42): Show |
45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1020+1491A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875476 | |||||||
chr3:32875547 | G | A | 45 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(42): Show |
45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1020+1562G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875547 | |||||||
chr3:32875596 | G | T | 45 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(42): Show |
45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1020+1611G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875596 | |||||||
chr3:32875664 | A | G | 1 | a0001c0001t0004g0143 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1020+1679A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875664 | |||||||
chr3:32875910 | A | C | 1 | a0001c0001t0001g0006 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1020+1925A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875910 | |||||||
chr3:32875923 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(106): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1020+1938G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875923 | |||||||
chr3:32875925 | T | A | 1 | a0001c0001t0001g0006 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1020+1940T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875925 | |||||||
chr3:32876016 | T | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0100 others(18): Show |
21 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1020+2031T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876016 | |||||||
chr3:32876090 | T | C | 2 | a0001c0002t0001g0234 a0001c0002t0002g0322 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1020+2105T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876090 | |||||||
chr3:32876252 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1020+2267C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876252 | |||||||
chr3:32876382 | G | A | 1 | a0001c0001t0033g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1020+2397G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876382 | |||||||
chr3:32876413 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1020+2428G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876413 | |||||||
chr3:32876562 | C | T | 7 | a0001c0001t0002g0067 a0001c0001t0002g0074 a0001c0001t0002g0077 others(4): Show |
7 | HG02970.hp1 HG03098.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020+2577C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876562 | |||||||
chr3:32876582 | T | TCAAA | 5 | a0001c0002t0002g0040 a0001c0002t0002g0122 a0001c0002t0002g0208 others(2): Show |
5 | HG00544.hp1 NA18962.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+2608_1020+261 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32876582 | ||||||
chr3:32876667 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0051g0096 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1020+2682A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876667 | |||||||
chr3:32876718 | G | A | 1 | a0001c0008t0007g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1020+2733G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876718 | |||||||
chr3:32876743 | C | T | 42 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(39): Show |
42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+2758C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876743 | |||||||
chr3:32876745 | C | A | 9 | a0001c0001t0007g0004 a0001c0001t0007g0069 a0001c0001t0007g0098 others(6): Show |
10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+2760C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876745 | |||||||
chr3:32876969 | G | A | 15 | a0001c0003t0005g0024 a0001c0003t0005g0027 a0001c0003t0005g0068 others(12): Show |
15 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1020+2984G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876969 | |||||||
chr3:32877005 | G | C | 1 | a0001c0002t0013g0256 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1020+3020G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877005 | |||||||
chr3:32877234 | G | C | 2 | a0001c0003t0005g0117 a0001c0003t0005g0321 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1020+3249G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877234 | |||||||
chr3:32877369 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1020+3384G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877369 | |||||||
chr3:32877404 | A | AT | 40 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0100 others(37): Show |
40 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.1020+3430dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32877404 | ||||||
chr3:32877404 | A | T | 1 | a0001c0001t0002g0232 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1020+3419A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877404 | |||||||
chr3:32877434 | C | G | 1 | a0001c0001t0008g0273 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1020+3449C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877434 | |||||||
chr3:32877483 | G | A | 11 | a0001c0001t0001g0075 a0001c0001t0002g0083 a0001c0001t0002g0118 others(8): Show |
11 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1020+3498G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877483 | |||||||
chr3:32877578 | C | T | 9 | a0001c0001t0002g0067 a0001c0001t0002g0074 a0001c0001t0002g0077 others(6): Show |
9 | HG02970.hp1 HG03098.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020+3593C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877578 | |||||||
chr3:32877699 | A | G | 42 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(39): Show |
42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+3714A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877699 | |||||||
chr3:32877795 | C | T | 3 | a0001c0001t0007g0098 a0001c0001t0007g0119 a0001c0001t0007g0121 |
3 | HG02451.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1020+3810C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877795 | |||||||
chr3:32878254 | C | T | 9 | a0001c0001t0002g0067 a0001c0001t0002g0074 a0001c0001t0002g0077 others(6): Show |
9 | HG02970.hp1 HG03098.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020+4269C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878254 | |||||||
chr3:32878327 | C | T | 1 | a0001c0001t0010g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1020+4342C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878327 | |||||||
chr3:32878366 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1020+4381T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878366 | |||||||
chr3:32878624 | A | AAATG | 25 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0100 others(22): Show |
25 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1020+4643_1020+464 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32878624 | ||||||
chr3:32878808 | A | G | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1020+4823A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878808 | |||||||
chr3:32878865 | C | A | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1020+4880C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878865 | |||||||
chr3:32878888 | C | G | 55 | a0001c0001t0002g0067 a0001c0001t0002g0074 a0001c0001t0002g0077 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1020+4903C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878888 | |||||||
chr3:32879018 | C | T | 37 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1020+5033C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879018 | |||||||
chr3:32879082 | TGTTTTCT others(2): Show |
T | 9 | a0001c0001t0007g0004 a0001c0001t0007g0069 a0001c0001t0007g0098 others(6): Show |
10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+5098_1020+510 others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879082 | |||||||
chr3:32879110 | G | C | 171 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0076 others(168): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1020+5125G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879110 | |||||||
chr3:32879112 | C | G | 46 | a0001c0001t0002g0067 a0001c0001t0002g0074 a0001c0001t0002g0077 others(43): Show |
46 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1020+5127C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879112 | |||||||
chr3:32879288 | C | T | 4 | a0001c0001t0016g0003 a0001c0001t0045g0071 a0001c0002t0002g0070 others(1): Show |
5 | HG02630.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1020+5303C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879288 | |||||||
chr3:32879402 | C | T | 1 | a0001c0001t0007g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1020+5417C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879402 | |||||||
chr3:32879409 | C | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(117): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1020+5424C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879409 | |||||||
chr3:32879430 | A | G | 2 | a0001c0001t0018g0099 a0001c0001t0018g0281 |
2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1020+5445A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879430 | |||||||
chr3:32879550 | T | C | 9 | a0001c0001t0007g0004 a0001c0001t0007g0069 a0001c0001t0007g0098 others(6): Show |
10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+5565T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879550 | |||||||
chr3:32879654 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1020+5669C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879654 | |||||||
chr3:32879672 | TA | T | 44 | a0001c0001t0001g0075 a0001c0001t0001g0238 a0001c0001t0001g0239 others(41): Show |
45 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1020+5703delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32879672 | ||||||
chr3:32879672 | TAA | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(177): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1020+5702_1020+570 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32879672 | ||||||
chr3:32879672 | TAAA | T | 41 | a0001c0001t0001g0006 a0001c0001t0003g0045 a0001c0001t0004g0036 others(38): Show |
41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1020+5701_1020+570 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32879672 | ||||||
chr3:32879675 | A | T | 4 | a0001c0002t0002g0287 a0001c0002t0002g0291 a0001c0002t0002g0292 others(1): Show |
4 | NA18945.hp2 NA18973.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020+5690A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879675 | |||||||
chr3:32879684 | A | C | 39 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0100 others(36): Show |
39 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.1020+5699A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879684 | |||||||
chr3:32879687 | A | T | 9 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 others(6): Show |
10 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+5702A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879687 | |||||||
chr3:32879696 | A | T | 1 | a0001c0002t0002g0129 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1020+5711A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879696 | |||||||
chr3:32879987 | T | C | 2 | a0001c0001t0018g0099 a0001c0001t0018g0281 |
2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1021-5947T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879987 | |||||||
chr3:32879998 | T | C | 4 | a0001c0001t0016g0003 a0001c0001t0045g0071 a0001c0002t0002g0070 others(1): Show |
5 | HG02630.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021-5936T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879998 | |||||||
chr3:32880094 | G | C | 9 | a0001c0001t0007g0004 a0001c0001t0007g0069 a0001c0001t0007g0098 others(6): Show |
10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1021-5840G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880094 | |||||||
chr3:32880276 | G | A | 8 | a0001c0001t0012g0010 a0001c0001t0012g0063 a0001c0001t0012g0169 others(5): Show |
8 | HG00323.hp1 HG01167.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-5658G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880276 | |||||||
chr3:32880390 | C | T | 1 | a0002c0005t0001g0159 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1021-5544C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880390 | |||||||
chr3:32880435 | T | A | 1 | a0001c0001t0007g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1021-5499T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880435 | |||||||
chr3:32880504 | T | A | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1021-5430T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880504 | |||||||
chr3:32880511 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1021-5423A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880511 | |||||||
chr3:32880826 | A | G | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1021-5108A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880826 | |||||||
chr3:32880917 | G | T | 3 | a0001c0001t0016g0079 a0001c0001t0026g0066 a0001c0001t0026g0319 |
3 | HG02723.hp1 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1021-5017G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880917 | |||||||
chr3:32880968 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1021-4966A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880968 | |||||||
chr3:32881009 | TTA | T | 4 | a0001c0001t0016g0003 a0001c0001t0045g0071 a0001c0002t0002g0070 others(1): Show |
5 | HG02630.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021-4919_1021-491 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32881009 | ||||||
chr3:32881017 | G | GTA | 8 | a0001c0001t0002g0074 a0001c0001t0002g0077 a0001c0001t0002g0232 others(5): Show |
8 | HG02559.hp1 HG02809.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-4905_1021-490 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32881017 | ||||||
chr3:32881029 | A | ATT | 38 | a0001c0001t0002g0082 a0001c0001t0002g0313 a0001c0001t0003g0045 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1021-4899_1021-489 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32881029 | ||||||
chr3:32881029 | A | T | 15 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0043 others(12): Show |
15 | HG00609.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1021-4905A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881029 | |||||||
chr3:32881031 | T | A | 4 | a0001c0001t0001g0075 a0001c0001t0018g0099 a0001c0001t0018g0281 others(1): Show |
4 | HG02559.hp2 HG03471.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-4903T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881031 | |||||||
chr3:32881093 | A | C | 54 | a0001c0001t0001g0054 a0001c0001t0001g0218 a0001c0001t0001g0219 others(51): Show |
54 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1021-4841A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881093 | |||||||
chr3:32881310 | C | T | 8 | a0001c0001t0007g0004 a0001c0001t0007g0098 a0001c0001t0007g0119 others(5): Show |
9 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021-4624C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881310 | |||||||
chr3:32881692 | A | G | 1 | a0001c0001t0016g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021-4242A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881692 | |||||||
chr3:32881839 | G | T | 8 | a0001c0001t0002g0074 a0001c0001t0002g0077 a0001c0001t0002g0082 others(5): Show |
8 | HG02970.hp1 HG03098.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-4095G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881839 | |||||||
chr3:32881846 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0051g0096 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1021-4088C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881846 | |||||||
chr3:32881852 | T | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1021-4082T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881852 | |||||||
chr3:32881924 | T | C | 1 | a0001c0001t0002g0314 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1021-4010T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881924 | |||||||
chr3:32881934 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1021-4000T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881934 | |||||||
chr3:32882148 | C | CA | 27 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0055 others(24): Show |
27 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1021-3785dupA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32882148 | ||||||
chr3:32882179 | C | CT | 45 | a0001c0001t0002g0074 a0001c0001t0002g0077 a0001c0001t0002g0082 others(42): Show |
45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1021-3746dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32882179 | ||||||
chr3:32882188 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0030 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021-3746T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882188 | |||||||
chr3:32882257 | TAGAA | T | 37 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1021-3674_1021-367 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32882257 | ||||||
chr3:32882542 | T | C | 2 | a0001c0001t0045g0071 a0001c0003t0005g0117 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1021-3392T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882542 | |||||||
chr3:32882598 | C | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0075 a0001c0001t0002g0067 others(15): Show |
18 | HG01192.hp1 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1021-3336C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882598 | |||||||
chr3:32882727 | A | G | 1 | a0001c0001t0009g0240 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1021-3207A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882727 | |||||||
chr3:32882733 | G | A | 91 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0002g0082 others(88): Show |
91 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1021-3201G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882733 | |||||||
chr3:32882803 | G | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(316): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1021-3131G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882803 | |||||||
chr3:32882845 | A | G | 2 | a0001c0001t0045g0071 a0001c0003t0005g0117 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1021-3089A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882845 | |||||||
chr3:32882882 | A | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1021-3052A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882882 | |||||||
chr3:32882892 | A | T | 1 | a0001c0001t0027g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1021-3042A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882892 | |||||||
chr3:32882985 | C | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021-2949C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882985 | |||||||
chr3:32883019 | ACT | A | 4 | a0001c0001t0009g0148 a0001c0001t0009g0224 a0001c0001t0009g0226 others(1): Show |
4 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-2910_1021-290 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32883019 | ||||||
chr3:32883034 | G | A | 37 | a0001c0001t0003g0045 a0001c0001t0004g0036 a0001c0001t0004g0037 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1021-2900G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883034 | |||||||
chr3:32883091 | T | A | 1 | a0001c0002t0002g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1021-2843T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883091 | |||||||
chr3:32883110 | A | T | 3 | a0001c0001t0002g0082 a0001c0001t0002g0313 a0001c0003t0005g0311 |
3 | HG03516.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1021-2824A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883110 | |||||||
chr3:32883249 | T | C | 2 | a0001c0001t0004g0061 a0001c0001t0004g0294 |
2 | NA18969.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1021-2685T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883249 | |||||||
chr3:32883310 | C | T | 14 | a0001c0003t0005g0024 a0001c0003t0005g0027 a0001c0003t0005g0068 others(11): Show |
14 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1021-2624C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883310 | |||||||
chr3:32883312 | G | A | 3 | a0001c0001t0003g0155 a0001c0001t0003g0200 a0001c0001t0003g0251 |
3 | HG00735.hp1 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1021-2622G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883312 | |||||||
chr3:32883330 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1021-2604A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883330 | |||||||
chr3:32883375 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1021-2559C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883375 | |||||||
chr3:32883542 | C | A | 13 | a0001c0001t0002g0067 a0001c0001t0002g0074 a0001c0001t0002g0077 others(10): Show |
13 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1021-2392C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883542 | |||||||
chr3:32884098 | C | T | 3 | a0001c0001t0002g0082 a0001c0001t0002g0313 a0001c0003t0005g0311 |
3 | HG03516.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1021-1836C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884098 | |||||||
chr3:32884298 | A | G | 1 | a0001c0001t0006g0167 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1021-1636A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884298 | |||||||
chr3:32884314 | T | C | 3 | a0001c0001t0002g0082 a0001c0001t0002g0313 a0001c0003t0005g0311 |
3 | HG03516.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1021-1620T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884314 | |||||||
chr3:32884317 | T | C | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1021-1617T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884317 | |||||||
chr3:32884433 | C | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1021-1501C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884433 | |||||||
chr3:32884456 | T | G | 40 | a0001c0001t0002g0082 a0001c0001t0002g0313 a0001c0001t0003g0045 others(37): Show |
40 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1021-1478T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884456 | |||||||
chr3:32884540 | GA | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(312): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1021-1380delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32884540 | ||||||
chr3:32884574 | A | G | 1 | a0001c0001t0012g0010 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1021-1360A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884574 | |||||||
chr3:32884613 | C | T | 1 | a0001c0002t0002g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1021-1321C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884613 | |||||||
chr3:32884614 | G | T | 14 | a0001c0003t0005g0024 a0001c0003t0005g0027 a0001c0003t0005g0068 others(11): Show |
14 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1021-1320G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884614 | |||||||
chr3:32884668 | G | C | 1 | a0001c0001t0002g0314 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1021-1266G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884668 | |||||||
chr3:32884671 | T | C | 6 | a0001c0001t0002g0083 a0001c0001t0002g0303 a0001c0001t0002g0306 others(3): Show |
6 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021-1263T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884671 | |||||||
chr3:32885058 | C | A | 1 | a0001c0001t0045g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1021-876C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885058 | |||||||
chr3:32885063 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1021-871C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885063 | |||||||
chr3:32885284 | T | TTTTTATG | 40 | a0001c0001t0002g0082 a0001c0001t0002g0313 a0001c0001t0003g0045 others(37): Show |
40 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1021-650_1021-649i others(9): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885284 | |||||||
chr3:32885491 | C | T | 3 | a0001c0001t0002g0082 a0001c0001t0002g0313 a0001c0003t0005g0311 |
3 | HG03516.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1021-443C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885491 | |||||||
chr3:32885494 | G | A | 15 | a0001c0003t0005g0024 a0001c0003t0005g0027 a0001c0003t0005g0068 others(12): Show |
15 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1021-440G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885494 | |||||||
chr3:32885496 | C | T | 9 | a0001c0001t0007g0004 a0001c0001t0007g0098 a0001c0001t0007g0119 others(6): Show |
10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1021-438C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885496 | |||||||
chr3:32885575 | G | T | 1 | a0001c0001t0003g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1021-359G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885575 | |||||||
chr3:32885660 | G | C | 1 | a0001c0001t0002g0314 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1021-274G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885660 | |||||||
chr3:32885833 | G | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021-101G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885833 | |||||||
chr3:32885908 | G | A | 67 | a0001c0002t0001g0234 a0001c0002t0002g0015 a0001c0002t0002g0016 others(64): Show |
67 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1021-26G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885908 | |||||||
chr3:32886180 | A | G | 2 | a0001c0003t0005g0117 a0001c0003t0005g0321 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1155+112A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886180 | |||||||
chr3:32886310 | T | C | 2 | a0001c0001t0018g0099 a0001c0001t0018g0281 |
2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1155+242T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886310 | |||||||
chr3:32886468 | C | T | 15 | a0001c0003t0005g0024 a0001c0003t0005g0027 a0001c0003t0005g0068 others(12): Show |
15 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1155+400C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886468 | |||||||
chr3:32886593 | A | G | 3 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 |
3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1155+525A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886593 | |||||||
chr3:32886672 | A | G | 32 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0002t0002g0039 others(29): Show |
32 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1155+604A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886672 | |||||||
chr3:32887322 | A | G | 1 | a0001c0001t0008g0271 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1155+1254A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887322 | |||||||
chr3:32887422 | T | C | 1 | a0001c0003t0005g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1155+1354T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887422 | |||||||
chr3:32887481 | C | CT | 39 | a0001c0001t0002g0083 a0001c0001t0002g0303 a0001c0001t0002g0306 others(36): Show |
40 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1155+1434dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32887481 | ||||||
chr3:32887481 | CT | C | 86 | a0001c0001t0001g0013 a0001c0001t0001g0075 a0001c0001t0001g0076 others(83): Show |
87 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1155+1434delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32887481 | ||||||
chr3:32887481 | CTT | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1155+1433_1155+143 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32887481 | ||||||
chr3:32887623 | T | C | 114 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0056 others(111): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1155+1555T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887623 | |||||||
chr3:32887660 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1155+1592C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887660 | |||||||
chr3:32887711 | C | CAT | 3 | a0001c0001t0016g0003 a0001c0001t0016g0079 a0001c0001t0045g0071 |
4 | HG02647.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155+1651_1155+165 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32887711 | ||||||
chr3:32887783 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1155+1715C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887783 | |||||||
chr3:32887789 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0302 a0001c0001t0001g0315 |
3 | HG02622.hp2 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1155+1721T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887789 | |||||||
chr3:32887836 | A | G | 1 | a0001c0001t0007g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1155+1768A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887836 | |||||||
chr3:32887850 | G | A | 9 | a0001c0001t0009g0090 a0001c0001t0009g0115 a0001c0001t0009g0148 others(6): Show |
9 | HG00140.hp1 HG01069.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+1782G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887850 | |||||||
chr3:32887991 | A | G | 1 | a0001c0002t0002g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1155+1923A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887991 | |||||||
chr3:32888105 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1155+2037T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888105 | |||||||
chr3:32888208 | T | G | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1155+2140T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888208 | |||||||
chr3:32888407 | G | A | 1 | a0001c0001t0020g0041 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1156-1953G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888407 | |||||||
chr3:32888427 | T | C | 1 | a0001c0001t0009g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1156-1933T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888427 | |||||||
chr3:32888434 | CAAAAAAA others(3): Show |
C | 10 | a0001c0001t0002g0067 a0001c0001t0002g0074 a0001c0001t0002g0077 others(7): Show |
10 | HG02040.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1156-1896_1156-188 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(4): Show |
C | 31 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0306 others(28): Show |
31 | HG00438.hp2 HG01891.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.1156-1897_1156-188 others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(5): Show |
C | 43 | a0001c0001t0002g0303 a0001c0001t0002g0307 a0001c0001t0002g0318 others(40): Show |
43 | HG00280.hp2 HG00597.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1156-1898_1156-188 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(6): Show |
C | 58 | a0001c0001t0001g0158 a0001c0001t0001g0164 a0001c0001t0001g0218 others(55): Show |
58 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1156-1899_1156-188 others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(7): Show |
C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0087 others(13): Show |
17 | HG01175.hp1 HG01255.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1156-1900_1156-188 others(18): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(8): Show |
C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.1156-1901_1156-188 others(19): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0138 a0001c0001t0001g0302 others(3): Show |
6 | HG00280.hp1 HG02735.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1156-1902_1156-188 others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(10): Show |
C | 9 | a0001c0001t0007g0004 a0001c0001t0007g0069 a0001c0001t0007g0098 others(6): Show |
10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1156-1903_1156-188 others(21): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1156-1905_1156-188 others(23): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(16): Show |
C | 35 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0056 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1156-1909_1156-188 others(27): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888434 | CAAAAAAA others(20): Show |
C | 1 | a0001c0001t0009g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1156-1913_1156-188 others(31): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | ||||||
chr3:32888473 | A | T | 105 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0056 others(102): Show |
107 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1156-1887A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888473 | |||||||
chr3:32888532 | T | TTTG | 14 | a0001c0001t0001g0013 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
15 | HG02258.hp2 HG02647.hp2 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.1156-1807_1156-180 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888532 | ||||||
chr3:32888622 | C | A | 1 | a0001c0001t0008g0266 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1156-1738C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888622 | |||||||
chr3:32888702 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.1156-1658G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888702 | |||||||
chr3:32888755 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0075 a0001c0001t0001g0076 others(10): Show |
13 | HG01081.hp1 HG02258.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1156-1605G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888755 | |||||||
chr3:32888839 | T | A | 36 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0056 others(33): Show |
36 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1156-1521T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888839 | |||||||
chr3:32888893 | G | A | 19 | a0001c0001t0016g0003 a0001c0001t0016g0079 a0001c0001t0045g0071 others(16): Show |
20 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.1156-1467G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888893 | |||||||
chr3:32889007 | C | T | 4 | a0001c0003t0005g0068 a0001c0003t0005g0282 a0001c0003t0005g0283 others(1): Show |
4 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-1353C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889007 | |||||||
chr3:32889077 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1156-1283C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889077 | |||||||
chr3:32889338 | C | T | 54 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0056 others(51): Show |
55 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1156-1022C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889338 | |||||||
chr3:32889360 | C | T | 1 | a0001c0001t0021g0174 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1156-1000C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889360 | |||||||
chr3:32889501 | G | GTAA | 54 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0056 others(51): Show |
55 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1156-856_1156-854d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889501 | ||||||
chr3:32889513 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1156-847C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889513 | |||||||
chr3:32889548 | C | T | 6 | a0001c0001t0010g0235 a0001c0001t0010g0236 a0001c0001t0010g0237 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1156-812C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889548 | |||||||
chr3:32889559 | A | AATT | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(120): Show |
124 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1156-758_1156-756d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | ||||||
chr3:32889559 | A | AATTATT | 23 | a0001c0001t0001g0110 a0001c0001t0001g0175 a0001c0001t0001g0214 others(20): Show |
23 | HG00140.hp1 HG00323.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1156-761_1156-756d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | ||||||
chr3:32889559 | A | AATTATTA others(2): Show |
4 | a0001c0001t0003g0200 a0001c0001t0008g0274 a0001c0001t0008g0276 others(1): Show |
4 | HG00609.hp2 HG02055.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-764_1156-756d others(11): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | ||||||
chr3:32889559 | AATT | A | 37 | a0001c0001t0002g0313 a0001c0001t0007g0004 a0001c0001t0007g0119 others(34): Show |
39 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1156-758_1156-756d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | ||||||
chr3:32889559 | AATTATT | A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0194 a0001c0001t0001g0196 others(4): Show |
7 | NA18747.hp2 NA18966.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156-761_1156-756d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | ||||||
chr3:32889617 | C | T | 1 | a0001c0002t0002g0146 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1156-743C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889617 | |||||||
chr3:32889628 | C | G | 104 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0056 others(101): Show |
106 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1156-732C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889628 | |||||||
chr3:32889645 | A | G | 6 | a0001c0001t0007g0004 a0001c0001t0007g0069 a0001c0001t0007g0308 others(3): Show |
7 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156-715A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889645 | |||||||
chr3:32889766 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1156-594T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889766 | |||||||
chr3:32889843 | A | G | 53 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0056 others(50): Show |
54 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1156-517A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889843 | |||||||
chr3:32889886 | A | ATG | 7 | a0001c0001t0002g0314 a0001c0001t0010g0235 a0001c0001t0010g0236 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156-460_1156-459d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889886 | ||||||
chr3:32889898 | GTGTA | G | 34 | a0001c0001t0003g0045 a0001c0001t0003g0055 a0001c0001t0003g0056 others(31): Show |
34 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1156-442_1156-439d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889898 | ||||||
chr3:32890173 | C | G | 16 | a0001c0003t0005g0024 a0001c0003t0005g0027 a0001c0003t0005g0068 others(13): Show |
16 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1156-187C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32890173 | |||||||
chr3:32890179 | T | C | 2 | a0001c0002t0002g0151 a0001c0002t0002g0160 |
2 | NA19003.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1156-181T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32890179 | |||||||
chr3:32890257 | T | C | 4 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0249 others(1): Show |
4 | HG01081.hp1 HG01981.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-103T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32890257 |