Item | Value |
---|---|
geneid | 9319 |
ensemblid | ENSG00000071539.14 |
hgncid | 12307 |
symbol | TRIP13 |
name | thyroid hormone receptor interactor 13 |
refseq_nuc | NM_004237.4 |
refseq_prot | NP_004228.1 |
ensembl_nuc | ENST00000166345.8 |
ensembl_prot | ENSP00000166345.3 |
mane_status | MANE Select |
chr | chr5 |
start | 892884 |
end | 918120 |
strand | + |
ver | v1.2 |
region | chr5:892884-918120 |
region5000 | chr5:887884-923120 |
regionname0 | TRIP13_chr5_892884_918120 |
regionname5000 | TRIP13_chr5_887884_923120 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 432 | 395 | 93 | 78 | 162 | 16 | 44 | 124 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0002 | 0/0 | 432 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0003 | 0/0 | 432 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0004 | 0/0 | 432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0005 | 0/0 | 432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0006 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1299 | 386 | 92 | 74 | 159 | 16 | 43 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0002 | 0/0 | 1299 | 4 | 0 | 3 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0003 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0004 | 0/0 | 1299 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0005 | 0/0 | 1299 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0006 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0007 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0008 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0009 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0010 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
c0011 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1133 | 268 | 30 | 48 | 140 | 14 | 34 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
t0002 | 0/0 | 1133 | 124 | 66 | 27 | 24 | 0 | 7 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
t0003 | 0/0 | 1133 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
t0004 | 0/0 | 1133 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
t0005 | 0/0 | 1133 | 2 | 0 | 0 | 0 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
t0006 | 0/0 | 1133 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
t0007 | 0/0 | 1133 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
t0008 | 0/0 | 1133 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
t0009 | 0/0 | 1133 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 39 | 1 | 9 | 19 | 3 | 7 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0002 | 0/0 | 21 | 0 | 10 | 8 | 0 | 3 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0003 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0005 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0006 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0008 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0009 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0027 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0052 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1299 | 386 | 92 | 74 | 159 | 16 | 43 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0002 | 0/0 | 1299 | 4 | 0 | 3 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0005 | 0/0 | 1299 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0007 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0009 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0010 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0002c0004 | 0/0 | 1299 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0003c0003 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0004c0008 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0005c0011 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0006c0006 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2431 | 261 | 30 | 48 | 133 | 14 | 34 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0001t0002 | 0/0 | 2431 | 115 | 62 | 23 | 24 | 0 | 6 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0001t0003 | 0/0 | 2431 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0001t0004 | 0/0 | 2431 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0001t0005 | 0/0 | 2431 | 2 | 0 | 0 | 0 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0001t0006 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0001t0007 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0001t0008 | 0/0 | 2431 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0001t0009 | 0/0 | 2431 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0002t0002 | 0/0 | 2431 | 4 | 0 | 3 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0005t0002 | 0/0 | 2431 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0007t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0009t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0001c0010t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0002c0004t0001 | 0/0 | 2431 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0003c0003t0002 | 0/0 | 2431 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0004c0008t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0005c0011t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
a0006c0006t0002 | 0/0 | 2431 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | copy fasta | chr5 | 887884 | 923120 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 37 | 1 | 8 | 19 | 2 | 7 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0005 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0027 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0002 | 0/0 | 21 | 0 | 10 | 8 | 0 | 3 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0008g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0001t0009g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0002t0002g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0005t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0005t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0007t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0009t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0001c0010t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0002c0004t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0003c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0003c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0004c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0005c0011t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
a0006c0006t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | GBR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | GBR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | FIN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00673 | hp2 | a0002 | c0004 | t0001 | g0053 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0112 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01243 | hp1 | a0001 | c0005 | t0002 | g0214 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0119 | EUR | IBS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02027 | hp1 | a0002 | c0004 | t0001 | g0053 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0072 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | CDX | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02698 | hp2 | a0001 | c0001 | t0008 | g0206 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02976 | hp2 | a0003 | c0003 | t0002 | g0025 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0038 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0038 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03540 | hp1 | a0003 | c0003 | t0002 | g0156 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03540 | hp2 | a0006 | c0006 | t0002 | g0025 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03579 | hp2 | a0001 | c0005 | t0002 | g0213 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18945 | hp1 | a0005 | c0011 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18952 | hp1 | a0001 | c0009 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18987 | hp1 | a0001 | c0010 | t0001 | g0046 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19003 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19012 | hp2 | a0001 | c0007 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | LWK | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19059 | hp2 | a0004 | c0008 | t0001 | g0182 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ASW | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ASW | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | GIH | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | USA | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | USA | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | USA | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | USA | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0100 | REF | REF | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0066 | REF | REF | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:896683
|
T | C | 2 | a0003a0006 | 3 | HG02976.hp2 HG03540.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.277T>C | p.Cys93Arg | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/13 | 392/2431 | 277/1299 | 93/432 | chr5 | 896683 | ||
chr5:901428
|
C | T | 1 | a0005 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.532C>T | p.His178Tyr | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/13 | 647/2431 | 532/1299 | 178/432 | chr5 | 901428 | ||
chr5:911847
|
T | A | 1 | a0004 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.871T>A | p.Ser291Thr | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/13 | 986/2431 | 871/1299 | 291/432 | chr5 | 911847 | ||
chr5:917030
|
G | A | 1 | a0006 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1226G>A | p.Gly409Glu | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 1341/2431 | 1226/1299 | 409/432 | chr5 | 917030 | ||
chr5:917098
|
A | G | 1 | a0002 | 2 | HG00673.hp2 HG02027.hp1 |
missense_variant | MODERATE | c.1294A>G | p.Ile432Val | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 1409/2431 | 1294/1299 | 432/432 | chr5 | 917098 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:907190
|
G | A | 1 | a0001c0007 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.669G>A | p.Ser223Ser | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/13 | 784/2431 | 669/1299 | 223/432 | chr5 | 907190 | ||
chr5:908420
|
C | T | 1 | a0001c0010 | 1 | NA18987.hp1 | synonymous_variant | LOW | c.825C>T | p.Arg275Arg | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/13 | 940/2431 | 825/1299 | 275/432 | chr5 | 908420 | ||
chr5:911882
|
C | G | 1 | a0001c0005 | 2 | HG01243.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.906C>G | p.Thr302Thr | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/13 | 1021/2431 | 906/1299 | 302/432 | chr5 | 911882 | ||
chr5:911903
|
C | T | 1 | a0001c0009 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.927C>T | p.Phe309Phe | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/13 | 1042/2431 | 927/1299 | 309/432 | chr5 | 911903 | ||
chr5:914549
|
T | C | 1 | a0001c0002 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
synonymous_variant | LOW | c.1105T>C | p.Leu369Leu | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/13 | 1220/2431 | 1105/1299 | 369/432 | chr5 | 914549 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:917209
|
G | A | 1 | a0001c0001t0006 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*106G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 106 | chr5 | 917209 | |||||
chr5:917236
|
A | C | 1 | a0001c0001t0005 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*133A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 133 | chr5 | 917236 | |||||
chr5:917296
|
T | C | 1 | a0001c0001t0007 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*193T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 193 | chr5 | 917296 | |||||
chr5:917479
|
G | T | 1 | a0001c0001t0004 | 2 | HG00735.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*376G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 376 | chr5 | 917479 | |||||
chr5:917549
|
G | A | 1 | a0001c0001t0008 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 446 | chr5 | 917549 | |||||
chr5:917582
|
T | G | 1 | a0001c0001t0003 | 2 | HG00140.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*479T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 479 | chr5 | 917582 | |||||
chr5:917763
|
A | G | 5 | a0001c0001t0002a0001c0002t0002a0001c0005t0002others(2): Show | 124 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*660A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 660 | chr5 | 917763 | |||||
chr5:918110
|
T | C | 1 | a0001c0001t0009 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1007T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 1007 | chr5 | 918110 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:893106
|
C | G | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+16C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893106 | ||||||
chr5:893106
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.92+16C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893106 | ||||||
chr5:893115
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.92+25C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893115 | ||||||
chr5:893241
|
C | G | 33 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0017others(30): Show | 60 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.92+151C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893241 | ||||||
chr5:893272
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | NA18980.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.92+182C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893272 | ||||||
chr5:893310
|
C | G | 12 | a0001c0001t0002g0018a0001c0001t0002g0028a0001c0001t0002g0054others(9): Show | 19 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.92+220C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893310 | ||||||
chr5:893337
|
T | A | 5 | a0001c0001t0002g0010a0001c0001t0002g0056a0001c0001t0002g0057others(2): Show | 13 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+247T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893337 | ||||||
chr5:893349
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.92+259C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893349 | ||||||
chr5:893377
|
ACCCTGC | A | 18 | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0014others(15): Show | 40 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.92+297_92+302delTG others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 893377 | |||||
chr5:893488
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.92+398G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893488 | ||||||
chr5:893510
|
G | C | 1 | a0001c0001t0002g0212 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92+420G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893510 | ||||||
chr5:893580
|
T | A | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+490T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893580 | ||||||
chr5:893649
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.92+559G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893649 | ||||||
chr5:893895
|
C | A | 1 | a0001c0001t0001g0062 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.92+805C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893895 | ||||||
chr5:894028
|
C | T | 1 | a0001c0001t0002g0011 | 5 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.93-759C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894028 | ||||||
chr5:894090
|
G | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(39): Show | 61 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.93-697G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894090 | ||||||
chr5:894245
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.93-542A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894245 | ||||||
chr5:894324
|
A | G | 36 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(33): Show | 65 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.93-463A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894324 | ||||||
chr5:894468
|
C | G | 36 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(33): Show | 65 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.93-319C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894468 | ||||||
chr5:894492
|
G | A | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.93-295G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894492 | ||||||
chr5:894508
|
G | A | 11 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0042others(8): Show | 21 | HG01175.hp2 HG01433.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-279G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894508 | ||||||
chr5:894542
|
G | A | 1 | a0001c0001t0001g0030 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.93-245G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894542 | ||||||
chr5:894976
|
A | C | 1 | a0001c0001t0006g0184 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.258+24A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 894976 | ||||||
chr5:894996
|
CA | C | 108 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(105): Show | 185 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.258+48delA | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 894996 | |||||
chr5:895287
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.258+335T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895287 | ||||||
chr5:895289
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.258+337G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895289 | ||||||
chr5:895488
|
GACTTATC | G | 30 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0024others(27): Show | 59 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.258+542_258+548del others(7): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 895488 | |||||
chr5:895558
|
G | C | 1 | a0001c0001t0001g0031 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.258+606G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895558 | ||||||
chr5:895561
|
C | A | 1 | a0001c0001t0006g0184 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.258+609C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895561 | ||||||
chr5:895567
|
G | A | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.258+615G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895567 | ||||||
chr5:895923
|
T | C | 5 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0188others(2): Show | 5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-742T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895923 | ||||||
chr5:896068
|
CTG | C | 1 | a0001c0001t0001g0019 | 3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.259-594_259-593del others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 896068 | |||||
chr5:896121
|
G | A | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.259-544G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896121 | ||||||
chr5:896140
|
C | T | 5 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0188others(2): Show | 5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-525C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896140 | ||||||
chr5:896158
|
T | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.259-507T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896158 | ||||||
chr5:896182
|
G | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-483G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896182 | ||||||
chr5:896218
|
G | T | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-447G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896218 | ||||||
chr5:896297
|
A | G | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-368A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896297 | ||||||
chr5:896429
|
C | T | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.259-236C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896429 | ||||||
chr5:896542
|
G | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-123G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896542 | ||||||
chr5:896611
|
C | G | 36 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(33): Show | 65 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.259-54C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896611 | ||||||
chr5:896867
|
C | CG | 7 | a0001c0001t0001g0158a0001c0001t0002g0010a0001c0001t0002g0186others(4): Show | 12 | HG02280.hp1 HG02486.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.388+73_388+74insG | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 896867 | ||||||
chr5:896868
|
A | G | 108 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(105): Show | 185 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.388+74A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 896868 | ||||||
chr5:896870
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.388+76G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 896870 | ||||||
chr5:897067
|
G | T | 1 | a0003c0003t0002g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.388+273G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897067 | ||||||
chr5:897138
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.388+344C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897138 | ||||||
chr5:897138
|
CGGCTTCA others(59): Show |
C | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.388+488_388+553del others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897138 | |||||
chr5:897189
|
A | G | 1 | a0001c0001t0001g0051 | 2 | NA18983.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.388+395A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897189 | ||||||
chr5:897223
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.388+429T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897223 | ||||||
chr5:897255
|
A | G | 1 | a0001c0001t0001g0051 | 2 | NA18983.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.388+461A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897255 | ||||||
chr5:897268
|
C | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.388+474C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897268 | ||||||
chr5:897282
|
G | T | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.388+488G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897282 | ||||||
chr5:897321
|
A | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0050others(9): Show | 18 | HG00140.hp2 HG00438.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.388+527A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897321 | ||||||
chr5:897345
|
TCATTCAG others(125): Show |
T | 4 | a0001c0001t0002g0013a0001c0001t0002g0059a0001c0005t0002g0213others(1): Show | 4 | HG01243.hp1 HG02896.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+554_388+685del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897345 | |||||
chr5:897348
|
T | G | 15 | a0001c0001t0001g0051a0001c0001t0002g0007a0001c0001t0002g0013others(12): Show | 35 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.388+554T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897348 | ||||||
chr5:897348
|
T | TTCAGTGT others(59): Show |
1 | a0001c0001t0002g0041 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.388+592_388+593ins others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897348
|
T | TTCAGTGT others(125): Show |
1 | a0001c0001t0002g0024 | 3 | NA18612.hp2 NA18947.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.388+592_388+593ins others(132): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897348
|
T | TTCAGTGT others(191): Show |
3 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148 | 3 | HG02300.hp1 NA18988.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.388+592_388+593ins others(198): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897348
|
T | TTCAGTGT others(59): Show |
1 | a0001c0001t0001g0048 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.388+617_388+682dup others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897348
|
TTCAGTGT others(125): Show |
T | 1 | a0001c0001t0001g0191 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.388+683_388+814del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897348
|
TTCAGTGT others(191): Show |
T | 7 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0045others(4): Show | 18 | HG00609.hp1 HG02080.hp1 NA18951.hp1 others(15): Show |
intron_variant | MODIFIER | c.388+683_388+880del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897348
|
TTCAGTGT others(323): Show |
T | 1 | a0001c0001t0001g0043 | 2 | HG02027.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.388+683_388+1012de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897348
|
TTCAGTGT others(653): Show |
T | 1 | a0001c0001t0002g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388+683_388+1342de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897348
|
TTCAGTGT others(983): Show |
T | 1 | a0001c0001t0001g0121 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.388+683_388+1672de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897348
|
TTCAGTGT others(1115): Show |
T | 1 | a0001c0001t0008g0206 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.388+683_388+1804de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | |||||
chr5:897376
|
G | GGATGGGC others(191): Show |
19 | a0001c0001t0002g0002a0001c0001t0002g0039a0001c0001t0002g0040others(16): Show | 41 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.388+592_388+593ins others(198): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897376 | |||||
chr5:897387
|
G | A | 38 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0011others(35): Show | 71 | HG01081.hp2 HG01099.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.388+593G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897387 | ||||||
chr5:897411
|
TCAGTCAG others(59): Show |
T | 11 | a0001c0001t0001g0031a0001c0001t0001g0068a0001c0001t0001g0069others(8): Show | 13 | HG00609.hp2 HG01106.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.388+683_388+748del others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897411 | |||||
chr5:897411
|
TCAGTCAG others(587): Show |
T | 3 | a0001c0001t0002g0010a0001c0001t0002g0057a0001c0001t0002g0058 | 8 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+683_388+1276de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897411 | |||||
chr5:897411
|
TCAGTCAG others(785): Show |
T | 1 | a0001c0002t0002g0012 | 3 | HG01175.hp2 HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.388+683_388+1474de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897411 | |||||
chr5:897411
|
TCAGTCAG others(851): Show |
T | 1 | a0001c0002t0002g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.388+683_388+1540de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897411 | |||||
chr5:897414
|
G | GTCAGTGT others(59): Show |
2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.388+658_388+659ins others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897414 | |||||
chr5:897434
|
G | A | 1 | a0001c0001t0002g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.388+640G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897434 | ||||||
chr5:897442
|
G | A | 1 | a0001c0001t0002g0024 | 3 | NA18612.hp2 NA18947.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.388+648G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897442 | ||||||
chr5:897453
|
G | A | 20 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0018others(17): Show | 38 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.388+659G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897453 | ||||||
chr5:897477
|
G | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.388+683G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897477 | ||||||
chr5:897508
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.388+714G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897508 | ||||||
chr5:897508
|
G | GGATGGGC others(59): Show |
2 | a0001c0001t0002g0011a0001c0001t0002g0041 | 6 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.388+779_388+780ins others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897508 | |||||
chr5:897519
|
G | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0059a0001c0001t0002g0145others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.388+725G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897519 | ||||||
chr5:897543
|
T | G | 2 | a0001c0001t0001g0051a0001c0001t0002g0128 | 3 | NA18948.hp2 NA18983.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.388+749T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897543 | ||||||
chr5:897574
|
G | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0017others(23): Show | 48 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.388+780G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897574 | ||||||
chr5:897585
|
G | A | 2 | a0001c0005t0002g0213a0001c0005t0002g0214 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.388+791G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897585 | ||||||
chr5:897640
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01106.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.388+846G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897640 | ||||||
chr5:897675
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.388+881T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897675 | ||||||
chr5:897696
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 9 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+902A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897696 | ||||||
chr5:897741
|
TCAGTCAG others(125): Show |
T | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1211_388+1342d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897741 | |||||
chr5:897741
|
TCAGTCAG others(257): Show |
T | 1 | a0001c0001t0002g0145 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.388+1079_388+1342d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897741 | |||||
chr5:897762
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 9 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+968A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897762 | ||||||
chr5:897807
|
T | G | 6 | a0001c0001t0001g0191a0001c0001t0002g0186a0001c0001t0002g0187others(3): Show | 6 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.388+1013T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897807 | ||||||
chr5:897807
|
T | TCAGTCAG others(59): Show |
2 | a0001c0001t0002g0024a0001c0001t0002g0126 | 4 | NA18612.hp2 NA18947.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+1079_388+1144d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897807 | |||||
chr5:897807
|
T | TCAGTCAG others(191): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0164 | 3 | HG02257.hp1 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.388+1078_388+1079i others(200): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897807 | |||||
chr5:897807
|
TCAGTCAG others(59): Show |
T | 4 | a0001c0001t0001g0051a0001c0001t0001g0120a0001c0001t0001g0176others(1): Show | 6 | HG01433.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.388+1079_388+1144d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897807 | |||||
chr5:897810
|
G | A | 1 | a0001c0001t0001g0050 | 2 | NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.388+1016G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897810 | ||||||
chr5:897828
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1034A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897828 | ||||||
chr5:897849
|
G | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0177a0001c0001t0001g0178others(4): Show | 9 | HG00438.hp1 NA18969.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.388+1055G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897849 | ||||||
chr5:897849
|
G | GGCAGGCC others(59): Show |
1 | a0001c0001t0001g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.388+1078_388+1079i others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897849 | |||||
chr5:897873
|
G | T | 58 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0046others(55): Show | 88 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.388+1079G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897873 | ||||||
chr5:897873
|
GCAGTCAG others(59): Show |
G | 10 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0045others(7): Show | 21 | HG00609.hp1 HG02080.hp1 HG03669.hp1 others(18): Show |
intron_variant | MODIFIER | c.388+1145_388+1210d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897873 | |||||
chr5:897873
|
GCAGTCAG others(323): Show |
G | 1 | a0001c0001t0001g0194 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.388+1211_388+1540d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897873 | |||||
chr5:897873
|
GCAGTCAG others(587): Show |
G | 1 | a0001c0001t0001g0031 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.388+1211_388+1804d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897873 | |||||
chr5:897873
|
GCAGTCAG others(719): Show |
G | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.388+1211_389-1764d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897873 | |||||
chr5:897894
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1100A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897894 | ||||||
chr5:897915
|
G | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0158a0001c0001t0001g0161others(6): Show | 9 | HG02886.hp1 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+1121G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897915 | ||||||
chr5:897939
|
T | G | 39 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0048others(36): Show | 68 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.388+1145T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897939 | ||||||
chr5:897939
|
T | TCAGTCAG others(59): Show |
1 | a0001c0001t0002g0011 | 5 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+1211_388+1276d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897939 | |||||
chr5:897939
|
TCAGTCAG others(59): Show |
T | 1 | a0001c0001t0001g0191 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.388+1211_388+1276d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897939 | |||||
chr5:897939
|
TCAGTCAG others(1049): Show |
T | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.388+1343_389-1302d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897939 | |||||
chr5:897960
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1166A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897960 | ||||||
chr5:898005
|
G | GCAGTCAG others(125): Show |
3 | a0001c0001t0001g0161a0001c0001t0001g0171a0001c0001t0002g0041 | 4 | HG02809.hp1 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+1276_388+1277i others(134): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | |||||
chr5:898005
|
G | GCAGTCAG others(125): Show |
1 | a0001c0001t0002g0040 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.389-1763_389-1632d others(134): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | |||||
chr5:898005
|
G | GCAGTCAG others(521): Show |
1 | a0001c0001t0001g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.388+1408_388+1409i others(530): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | |||||
chr5:898005
|
G | GCAGTCAG others(587): Show |
1 | a0001c0001t0001g0082 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.388+1408_388+1409i others(596): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | |||||
chr5:898005
|
G | T | 29 | a0001c0001t0001g0047a0001c0001t0001g0164a0001c0001t0001g0175others(26): Show | 50 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.388+1211G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898005 | ||||||
chr5:898005
|
GCAGTCAG others(455): Show |
G | 1 | a0001c0001t0001g0086 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.388+1607_389-1632d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | |||||
chr5:898005
|
GCAGTCAG others(1577): Show |
G | 1 | a0001c0001t0001g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.388+1277_389-840de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | |||||
chr5:898008
|
G | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.388+1214G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898008 | ||||||
chr5:898026
|
A | G | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0059others(2): Show | 11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.388+1232A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898026 | ||||||
chr5:898047
|
G | A | 3 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058 | 3 | HG02280.hp2 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.388+1253G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898047 | ||||||
chr5:898058
|
CCCAGGGC others(58): Show |
C | 1 | a0004c0008t0001g0182 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.388+1267_388+1331d others(67): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898058 | |||||
chr5:898071
|
T | G | 43 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0026others(40): Show | 54 | HG00438.hp1 HG00609.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.388+1277T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898071 | ||||||
chr5:898071
|
T | TCAGTCAG others(191): Show |
1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.388+1408_388+1409i others(200): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898071 | |||||
chr5:898071
|
TCAGTCAG others(785): Show |
T | 1 | a0001c0001t0001g0080 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.388+1409_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898071 | |||||
chr5:898074
|
G | T | 1 | a0001c0001t0002g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388+1280G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898074 | ||||||
chr5:898074
|
GTCAGTGT others(1771): Show |
G | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(2): Show | 10 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1385_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898074 | |||||
chr5:898092
|
A | G | 2 | a0001c0001t0002g0013a0001c0001t0002g0059 | 2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.388+1298A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898092 | ||||||
chr5:898113
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388+1319G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898113 | ||||||
chr5:898137
|
T | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 23 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.388+1343T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898137 | ||||||
chr5:898158
|
A | G | 2 | a0001c0001t0002g0013a0001c0001t0002g0059 | 2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.388+1364A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898158 | ||||||
chr5:898203
|
T | G | 4 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0131others(1): Show | 5 | HG01099.hp2 HG02273.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+1409T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898203 | ||||||
chr5:898206
|
GTCAGTGT others(1639): Show |
G | 3 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0149 | 9 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+1517_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898206 | |||||
chr5:898224
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1430A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898224 | ||||||
chr5:898245
|
G | A | 1 | a0001c0002t0002g0012 | 3 | HG01175.hp2 HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.388+1451G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898245 | ||||||
chr5:898269
|
T | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0194a0001c0001t0005g0038 | 4 | HG01106.hp1 HG02083.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+1475T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898269 | ||||||
chr5:898271
|
A | G | 4 | a0001c0001t0002g0186a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 4 | HG02280.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+1477A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898271 | ||||||
chr5:898272
|
G | A | 1 | a0001c0001t0001g0017 | 4 | NA18945.hp2 NA18965.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+1478G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898272 | ||||||
chr5:898272
|
GTCAGTGT others(1573): Show |
G | 6 | a0001c0001t0002g0018a0001c0001t0002g0028a0001c0001t0002g0029others(3): Show | 14 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.388+1583_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898272 | |||||
chr5:898290
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1496A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898290 | ||||||
chr5:898311
|
G | A | 1 | a0001c0002t0002g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.388+1517G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898311 | ||||||
chr5:898335
|
T | G | 4 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0191others(1): Show | 5 | HG01981.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+1541T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898335 | ||||||
chr5:898335
|
T | TCAGTCAG others(455): Show |
1 | a0001c0001t0001g0048 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.389-1764_389-1763i others(464): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898335 | |||||
chr5:898337
|
A | G | 2 | a0001c0001t0002g0186a0001c0001t0002g0190 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.388+1543A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898337 | ||||||
chr5:898356
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1562A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898356 | ||||||
chr5:898401
|
T | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0043others(10): Show | 28 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.388+1607T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898401 | ||||||
chr5:898401
|
TCAGTCAG others(455): Show |
T | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(82): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.388+1739_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898401 | |||||
chr5:898401
|
TCAGTCAG others(653): Show |
T | 3 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0203 | 3 | HG01952.hp2 HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.388+1739_389-1302d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898401 | |||||
chr5:898401
|
TCAGTCAG others(851): Show |
T | 1 | a0001c0001t0001g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.388+1805_389-1038d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898401 | |||||
chr5:898422
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1628A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898422 | ||||||
chr5:898467
|
T | G | 2 | a0001c0001t0001g0082a0001c0001t0002g0145 | 2 | HG01109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.388+1673T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898467 | ||||||
chr5:898467
|
TCAGTCAG others(389): Show |
T | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0033others(4): Show | 14 | HG01167.hp2 HG01934.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.388+1805_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898467 | |||||
chr5:898467
|
TCAGTCAG others(521): Show |
T | 1 | a0001c0001t0001g0090 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.388+1739_389-1434d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898467 | |||||
chr5:898467
|
TCAGTCAG others(719): Show |
T | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.388+1739_389-1236d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898467 | |||||
chr5:898470
|
GTCAGTGT others(1375): Show |
G | 1 | a0001c0005t0002g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.388+1781_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898470 | |||||
chr5:898488
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1694A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898488 | ||||||
chr5:898533
|
T | G | 4 | a0001c0001t0001g0051a0001c0001t0001g0081a0001c0001t0001g0088others(1): Show | 5 | HG00735.hp2 HG01109.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+1739T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898533 | ||||||
chr5:898533
|
TCAGTCAG others(323): Show |
T | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG00609.hp2 HG03669.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.389-1829_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898533 | |||||
chr5:898536
|
GTCAGTGT others(1309): Show |
G | 1 | a0001c0005t0002g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.388+1847_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898536 | |||||
chr5:898545
|
T | G | 1 | a0004c0008t0001g0182 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.388+1751T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898545 | ||||||
chr5:898554
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1760A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898554 | ||||||
chr5:898586
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.388+1792C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898586 | ||||||
chr5:898599
|
T | G | 2 | a0001c0001t0001g0088a0001c0001t0009g0119 | 2 | HG01516.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.388+1805T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898599 | ||||||
chr5:898599
|
TCAGTCAG others(257): Show |
T | 2 | a0001c0001t0001g0051a0001c0001t0005g0038 | 4 | HG03491.hp1 HG03492.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.389-1763_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898599 | |||||
chr5:898611
|
TGGGGAAA others(390): Show |
T | 1 | a0001c0001t0001g0088 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.388+1821_389-1483d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898611 | |||||
chr5:898665
|
T | G | 4 | a0001c0001t0001g0159a0001c0001t0002g0042a0001c0001t0002g0151others(1): Show | 7 | HG01175.hp2 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-1829T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898665 | ||||||
chr5:898665
|
TCAGTCAG others(191): Show |
T | 1 | a0001c0001t0001g0176 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.389-1697_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898665 | |||||
chr5:898707
|
G | GGCAGGCC others(125): Show |
1 | a0001c0001t0001g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389-1656_389-1655i others(134): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898707 | |||||
chr5:898731
|
T | G | 7 | a0001c0001t0001g0159a0001c0001t0001g0169a0001c0001t0002g0010others(4): Show | 12 | HG01109.hp1 HG01516.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.389-1763T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898731 | ||||||
chr5:898773
|
G | GGCAGGCC others(58): Show |
1 | a0001c0001t0002g0146 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.389-1719_389-1655d others(67): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898773 | |||||
chr5:898797
|
T | G | 2 | a0001c0001t0002g0058a0001c0001t0009g0119 | 2 | HG01516.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.389-1697T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898797 | ||||||
chr5:898797
|
TCAGTCAG others(59): Show |
T | 18 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0044others(15): Show | 37 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.389-1631_389-1566d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898797 | |||||
chr5:898797
|
TCAGTCAG others(455): Show |
T | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-1631_389-1170d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898797 | |||||
chr5:898839
|
G | AGCAGGCC others(917): Show |
1 | a0001c0001t0001g0047 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.389-1656_389-1655i others(926): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898839 | ||||||
chr5:898863
|
G | GCAGTCAG others(59): Show |
1 | a0001c0001t0001g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.389-1565_389-1500d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898863 | |||||
chr5:898863
|
G | T | 70 | a0001c0001t0001g0031a0001c0001t0001g0043a0001c0001t0001g0046others(67): Show | 108 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.389-1631G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898863 | ||||||
chr5:898863
|
GCAGTCAG others(59): Show |
G | 2 | a0001c0001t0001g0194a0001c0001t0002g0057 | 2 | HG01106.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.389-1565_389-1500d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898863 | |||||
chr5:898929
|
T | G | 17 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0032others(14): Show | 28 | HG00609.hp2 HG01167.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.389-1565T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898929 | ||||||
chr5:898929
|
T | TCAGTCAG others(1049): Show |
1 | a0001c0001t0001g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.389-1524_389-1523i others(1058): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898929 | |||||
chr5:898929
|
T | TCAGTCAG others(59): Show |
1 | a0001c0001t0001g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.389-1433_389-1368d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898929 | |||||
chr5:898950
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.389-1544A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898950 | ||||||
chr5:898995
|
G | T | 23 | a0001c0001t0001g0048a0001c0001t0001g0161a0001c0001t0001g0164others(20): Show | 48 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.389-1499G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898995 | ||||||
chr5:898995
|
GCAGTCAG others(125): Show |
G | 1 | a0001c0001t0001g0191 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.389-1367_389-1236d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898995 | |||||
chr5:899016
|
A | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0058 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.389-1478A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899016 | ||||||
chr5:899037
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.389-1457G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899037 | ||||||
chr5:899061
|
G | T | 62 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(59): Show | 91 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.389-1433G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899061 | ||||||
chr5:899061
|
GCAGTCAG others(59): Show |
G | 3 | a0001c0001t0001g0176a0001c0001t0002g0056a0001c0002t0002g0012 | 5 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-1367_389-1302d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899061 | |||||
chr5:899082
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.389-1412A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899082 | ||||||
chr5:899120
|
G | C | 1 | a0001c0001t0001g0196 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.389-1374G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899120 | ||||||
chr5:899127
|
T | G | 19 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0033others(16): Show | 27 | HG00609.hp2 HG01167.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.389-1367T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899127 | ||||||
chr5:899127
|
TCAGTCAG others(59): Show |
T | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.389-1235_389-1170d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899127 | |||||
chr5:899143
|
G | GAAACAGG others(59): Show |
1 | a0001c0001t0002g0143 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.389-1302_389-1301i others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899143 | |||||
chr5:899148
|
A | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.389-1346A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899148 | ||||||
chr5:899193
|
G | T | 23 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0090others(20): Show | 51 | HG00408.hp2 HG00621.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.389-1301G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899193 | ||||||
chr5:899214
|
A | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.389-1280A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899214 | ||||||
chr5:899259
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389-1235G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899259 | ||||||
chr5:899259
|
GCAGT | G | 5 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0188others(2): Show | 5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-1230_389-1227d others(6): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899259 | |||||
chr5:899259
|
GCAGTCAG others(59): Show |
G | 2 | a0001c0001t0002g0056a0001c0001t0002g0155 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.389-1103_389-1038d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899259 | |||||
chr5:899280
|
A | G | 2 | a0001c0001t0002g0057a0001c0002t0002g0012 | 5 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-1214A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899280 | ||||||
chr5:899325
|
T | G | 26 | a0001c0001t0001g0090a0001c0001t0001g0118a0001c0001t0001g0170others(23): Show | 54 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.389-1169T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899325 | ||||||
chr5:899325
|
TCAGTCAG others(125): Show |
T | 1 | a0001c0001t0001g0185 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.389-1103_389-972de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899325 | |||||
chr5:899325
|
TCAGTCAG others(191): Show |
T | 5 | a0001c0001t0001g0051a0001c0001t0001g0176a0001c0001t0002g0010others(2): Show | 11 | HG01109.hp1 HG02486.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.389-839_389-642del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899325 | |||||
chr5:899346
|
A | G | 3 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0002t0002g0012 | 6 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-1148A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899346 | ||||||
chr5:899369
|
C | G | 1 | a0001c0001t0007g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.389-1125C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899369 | ||||||
chr5:899390
|
TTCAGTCA others(195): Show |
T | 1 | a0001c0001t0009g0119 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.389-1098_389-897de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899390 | |||||
chr5:899391
|
T | G | 60 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(57): Show | 81 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(78): Show |
intron_variant | MODIFIER | c.389-1103T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899391 | ||||||
chr5:899391
|
T | TCAGTCAG others(2237): Show |
1 | a0001c0001t0001g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389-1038_389-1037i others(2246): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899391 | |||||
chr5:899391
|
TCAGTCAG others(257): Show |
T | 1 | a0001c0001t0002g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.389-971_389-708del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899391 | |||||
chr5:899412
|
A | G | 3 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0002t0002g0012 | 6 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-1082A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899412 | ||||||
chr5:899457
|
G | T | 4 | a0001c0001t0001g0178a0001c0001t0002g0042a0001c0001t0002g0059others(1): Show | 5 | HG01891.hp2 HG03209.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-1037G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899457 | ||||||
chr5:899523
|
G | GCAGTCAG others(59): Show |
21 | a0001c0001t0001g0048a0001c0001t0001g0161a0001c0001t0001g0170others(18): Show | 43 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.389-905_389-840dup others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899523 | |||||
chr5:899523
|
G | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(55): Show | 80 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(77): Show |
intron_variant | MODIFIER | c.389-971G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899523 | ||||||
chr5:899544
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-950A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899544 | ||||||
chr5:899589
|
T | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0075a0001c0001t0001g0120others(2): Show | 7 | HG00738.hp2 HG01192.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-905T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899589 | ||||||
chr5:899589
|
TCAGTCAG others(125): Show |
T | 1 | a0001c0001t0002g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.389-839_389-708del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899589 | |||||
chr5:899592
|
GTCAGTGT others(253): Show |
G | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.389-839_389-580del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899592 | |||||
chr5:899610
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-884A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899610 | ||||||
chr5:899655
|
G | GCAGTCAG others(59): Show |
1 | a0001c0001t0002g0133 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.389-774_389-773ins others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899655 | |||||
chr5:899655
|
G | T | 47 | a0001c0001t0001g0118a0001c0001t0002g0002a0001c0001t0002g0010others(44): Show | 84 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.389-839G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899655 | ||||||
chr5:899676
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-818A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899676 | ||||||
chr5:899721
|
G | T | 21 | a0001c0001t0001g0120a0001c0001t0001g0167a0001c0001t0001g0197others(18): Show | 29 | HG01175.hp2 HG01433.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.389-773G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899721 | ||||||
chr5:899722
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.389-772C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899722 | ||||||
chr5:899727
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.389-767A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899727 | ||||||
chr5:899763
|
G | A | 3 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058 | 3 | HG02280.hp2 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.389-731G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899763 | ||||||
chr5:899787
|
T | G | 2 | a0001c0001t0001g0069a0001c0001t0002g0134 | 2 | HG01928.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.389-707T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899787 | ||||||
chr5:899790
|
GTCAGTGT others(55): Show |
G | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-636_389-575del others(62): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899790 | |||||
chr5:899829
|
G | A | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-665G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899829 | ||||||
chr5:899852
|
T | TTCAG | 2 | a0001c0001t0001g0034a0001c0001t0002g0187 | 3 | HG02273.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.389-640_389-637dup others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899852 | |||||
chr5:899891
|
G | A | 8 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0056others(5): Show | 17 | HG01175.hp2 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.389-603G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899891 | ||||||
chr5:899957
|
A | G | 37 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0024others(34): Show | 67 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.389-537A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899957 | ||||||
chr5:899972
|
G | A | 1 | a0004c0008t0001g0182 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.389-522G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899972 | ||||||
chr5:899981
|
T | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.389-513T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899981 | ||||||
chr5:900041
|
A | G | 16 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0014others(13): Show | 36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.389-453A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900041 | ||||||
chr5:900145
|
C | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.389-349C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900145 | ||||||
chr5:900160
|
A | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.389-334A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900160 | ||||||
chr5:900175
|
T | G | 108 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(105): Show | 185 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.389-319T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900175 | ||||||
chr5:900220
|
C | T | 1 | a0001c0001t0002g0189 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.389-274C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900220 | ||||||
chr5:900569
|
C | T | 1 | a0004c0008t0001g0182 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.444+20C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900569 | ||||||
chr5:900642
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0091 | 2 | NA18961.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.444+93G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900642 | ||||||
chr5:900659
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0116 | 2 | HG00280.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.444+110C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900659 | ||||||
chr5:900724
|
T | C | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+175T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900724 | ||||||
chr5:900765
|
C | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.444+216C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900765 | ||||||
chr5:900799
|
G | A | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0059others(2): Show | 11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+250G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900799 | ||||||
chr5:900944
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.444+395T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900944 | ||||||
chr5:900964
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | NA18943.hp1 NA18960.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.445-377G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900964 | ||||||
chr5:901004
|
A | G | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.445-337A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901004 | ||||||
chr5:901079
|
T | A | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-262T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901079 | ||||||
chr5:901229
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0075a0001c0001t0001g0115 | 5 | NA18950.hp2 NA19056.hp1 NA19080.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-112C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901229 | ||||||
chr5:901232
|
C | T | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-109C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901232 | ||||||
chr5:901308
|
T | C | 16 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0014others(13): Show | 36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.445-33T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901308 | ||||||
chr5:901438
|
T | C | 5 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0188others(2): Show | 5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.535+7T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901438 | ||||||
chr5:901518
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.535+87G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901518 | ||||||
chr5:901604
|
TTTTGTTT others(1): Show |
T | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.535+185_535+192del others(8): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 901604 | |||||
chr5:901747
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.535+316C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901747 | ||||||
chr5:901843
|
A | G | 8 | a0001c0001t0002g0025a0001c0001t0002g0152a0001c0001t0002g0153others(5): Show | 8 | HG02572.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.535+412A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901843 | ||||||
chr5:901868
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.535+437C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901868 | ||||||
chr5:901943
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 7 | HG02273.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.535+512G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901943 | ||||||
chr5:902011
|
A | G | 16 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0014others(13): Show | 36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.535+580A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902011 | ||||||
chr5:902205
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.535+774G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902205 | ||||||
chr5:902220
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.535+789G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902220 | ||||||
chr5:902243
|
T | G | 13 | a0001c0001t0002g0025a0001c0001t0002g0152a0001c0001t0002g0153others(10): Show | 13 | HG02280.hp1 HG02572.hp2 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.535+812T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902243 | ||||||
chr5:902465
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0034others(2): Show | 10 | HG02109.hp1 HG02145.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.535+1034C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902465 | ||||||
chr5:902560
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.535+1129C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902560 | ||||||
chr5:902563
|
C | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.535+1132C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902563 | ||||||
chr5:902587
|
G | A | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.535+1156G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902587 | ||||||
chr5:902590
|
G | T | 1 | a0004c0008t0001g0182 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.535+1159G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902590 | ||||||
chr5:902614
|
A | G | 16 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0014others(13): Show | 36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.535+1183A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902614 | ||||||
chr5:902674
|
T | TAAAAG | 20 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0014others(17): Show | 43 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.535+1245_535+1249d others(7): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 902674 | |||||
chr5:902699
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.535+1268C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902699 | ||||||
chr5:902853
|
C | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.536-1295C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902853 | ||||||
chr5:902895
|
CAGAG | C | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0059others(2): Show | 11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.536-1249_536-1246d others(6): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 902895 | |||||
chr5:902902
|
A | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-1246A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902902 | ||||||
chr5:902910
|
C | T | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0059others(2): Show | 11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.536-1238C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902910 | ||||||
chr5:902941
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0193 | 3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.536-1207G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902941 | ||||||
chr5:902968
|
C | G | 2 | a0001c0001t0004g0112a0001c0001t0004g0113 | 2 | HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.536-1180C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902968 | ||||||
chr5:903018
|
G | A | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | NA18988.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.536-1130G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903018 | ||||||
chr5:903036
|
A | G | 1 | a0001c0001t0001g0037 | 2 | HG00099.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.536-1112A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903036 | ||||||
chr5:903073
|
C | T | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.536-1075C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903073 | ||||||
chr5:903126
|
C | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-1022C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903126 | ||||||
chr5:903162
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.536-986G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903162 | ||||||
chr5:903206
|
A | G | 107 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0036others(104): Show | 185 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.536-942A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903206 | ||||||
chr5:903233
|
G | C | 12 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0018others(9): Show | 31 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.536-915G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903233 | ||||||
chr5:903309
|
C | T | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-839C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903309 | ||||||
chr5:903345
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.536-803C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903345 | ||||||
chr5:903415
|
T | C | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.536-733T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903415 | ||||||
chr5:903484
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG00621.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.536-664C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903484 | ||||||
chr5:903535
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0087 | 3 | HG02015.hp1 HG02523.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.536-613G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903535 | ||||||
chr5:903540
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.536-608C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903540 | ||||||
chr5:903644
|
A | G | 1 | a0001c0001t0002g0142 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.536-504A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903644 | ||||||
chr5:903897
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.536-251G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903897 | ||||||
chr5:903967
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0158a0001c0001t0001g0163others(1): Show | 4 | NA18949.hp2 NA18965.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-181C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903967 | ||||||
chr5:904010
|
C | T | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0059others(2): Show | 11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.536-138C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 904010 | ||||||
chr5:904259
|
T | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0017others(22): Show | 45 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.608+39T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904259 | ||||||
chr5:904280
|
G | GT | 6 | a0001c0001t0001g0109a0001c0001t0001g0158a0001c0001t0001g0162others(3): Show | 9 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.608+73dupT | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 904280 | |||||
chr5:904280
|
GT | G | 13 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0018others(10): Show | 32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.608+73delT | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 904280 | |||||
chr5:904455
|
A | G | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.608+235A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904455 | ||||||
chr5:904480
|
G | C | 1 | a0001c0001t0001g0031 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.608+260G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904480 | ||||||
chr5:904609
|
A | T | 1 | a0001c0001t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.608+389A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904609 | ||||||
chr5:904619
|
C | A | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.608+399C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904619 | ||||||
chr5:904619
|
C | G | 5 | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0014others(2): Show | 16 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.608+399C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904619 | ||||||
chr5:904857
|
A | T | 3 | a0001c0001t0002g0007a0001c0001t0002g0029a0001c0001t0002g0150 | 10 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.608+637A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904857 | ||||||
chr5:904970
|
T | G | 1 | a0001c0001t0002g0129 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.608+750T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904970 | ||||||
chr5:905005
|
A | T | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.608+785A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905005 | ||||||
chr5:905076
|
AGT | A | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0059others(2): Show | 11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.608+859_608+860del others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 905076 | |||||
chr5:905319
|
G | A | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.608+1099G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905319 | ||||||
chr5:905332
|
A | G | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.608+1112A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905332 | ||||||
chr5:905347
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.608+1127G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905347 | ||||||
chr5:905354
|
G | C | 1 | a0001c0001t0004g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.608+1134G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905354 | ||||||
chr5:905394
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.608+1174G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905394 | ||||||
chr5:905578
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.608+1358G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905578 | ||||||
chr5:905760
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.609-1370G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905760 | ||||||
chr5:905978
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.609-1152G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905978 | ||||||
chr5:905996
|
A | G | 15 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(12): Show | 32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.609-1134A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905996 | ||||||
chr5:906052
|
C | CA | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 26 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.609-1071dupA | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 906052 | |||||
chr5:906272
|
C | T | 1 | a0004c0008t0001g0182 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.609-858C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906272 | ||||||
chr5:906280
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.609-850A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906280 | ||||||
chr5:906284
|
T | TC | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.609-845dupC | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 906284 | |||||
chr5:906344
|
T | TTG | 15 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(12): Show | 32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.609-785_609-784ins others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 906344 | |||||
chr5:906367
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.609-763A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906367 | ||||||
chr5:906515
|
A | G | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0164others(1): Show | 6 | HG02257.hp1 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.609-615A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906515 | ||||||
chr5:906716
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.609-414C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906716 | ||||||
chr5:906888
|
T | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0164a0001c0001t0001g0165 | 4 | HG02257.hp1 HG02258.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.609-242T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906888 | ||||||
chr5:906979
|
C | T | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.609-151C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906979 | ||||||
chr5:907008
|
A | G | 2 | a0001c0001t0002g0028a0001c0001t0002g0055 | 5 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.609-122A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 907008 | ||||||
chr5:907058
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.609-72C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 907058 | ||||||
chr5:907304
|
G | T | 1 | a0004c0008t0001g0182 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.672+111G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907304 | ||||||
chr5:907305
|
T | G | 1 | a0004c0008t0001g0182 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.672+112T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907305 | ||||||
chr5:907390
|
G | A | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.672+197G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907390 | ||||||
chr5:907405
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.672+212A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907405 | ||||||
chr5:907413
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.672+220C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907413 | ||||||
chr5:907564
|
C | T | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.672+371C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907564 | ||||||
chr5:907583
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.672+390G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907583 | ||||||
chr5:907601
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.673-387G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907601 | ||||||
chr5:907820
|
T | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.673-168T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907820 | ||||||
chr5:907941
|
C | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.673-47C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907941 | ||||||
chr5:908091
|
A | G | 1 | a0001c0001t0001g0033 | 2 | NA18990.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.759+17A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 8/12 | chr5 | 908091 | ||||||
chr5:908312
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.760-43G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 8/12 | chr5 | 908312 | ||||||
chr5:908316
|
G | C | 1 | a0001c0001t0001g0030 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.760-39G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 8/12 | chr5 | 908316 | ||||||
chr5:908473
|
A | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.866+12A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908473 | ||||||
chr5:908475
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0196a0001c0009t0001g0005 | 11 | HG02004.hp2 HG02015.hp2 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.866+14G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908475 | ||||||
chr5:908481
|
A | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.866+20A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908481 | ||||||
chr5:908534
|
T | C | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.866+73T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908534 | ||||||
chr5:908610
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.866+149T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908610 | ||||||
chr5:908647
|
T | A | 2 | a0001c0001t0002g0013a0001c0001t0002g0060 | 5 | HG02451.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.866+186T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908647 | ||||||
chr5:908659
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.866+198G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908659 | ||||||
chr5:908814
|
T | C | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.866+353T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908814 | ||||||
chr5:908815
|
G | A | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.866+354G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908815 | ||||||
chr5:908819
|
A | G | 107 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(104): Show | 184 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.866+358A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908819 | ||||||
chr5:908885
|
G | C | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.866+424G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908885 | ||||||
chr5:908907
|
G | A | 8 | a0001c0001t0002g0025a0001c0001t0002g0152a0001c0001t0002g0153others(5): Show | 8 | HG02572.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.866+446G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908907 | ||||||
chr5:908953
|
G | C | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.866+492G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908953 | ||||||
chr5:909039
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.866+578C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909039 | ||||||
chr5:909062
|
T | C | 5 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0188others(2): Show | 5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.866+601T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909062 | ||||||
chr5:909208
|
C | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0075a0001c0001t0001g0095others(1): Show | 6 | HG02132.hp2 NA18950.hp2 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.866+747C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909208 | ||||||
chr5:909284
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(29): Show | 50 | HG00438.hp1 HG00609.hp1 HG02027.hp2 others(47): Show |
intron_variant | MODIFIER | c.866+823C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909284 | ||||||
chr5:909301
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.866+840G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909301 | ||||||
chr5:909444
|
C | T | 1 | a0001c0001t0002g0189 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.866+983C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909444 | ||||||
chr5:909505
|
C | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(24): Show | 43 | HG00438.hp1 HG00609.hp1 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.866+1044C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909505 | ||||||
chr5:909506
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.866+1045G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909506 | ||||||
chr5:909641
|
C | T | 8 | a0001c0001t0002g0025a0001c0001t0002g0152a0001c0001t0002g0153others(5): Show | 8 | HG02572.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.866+1180C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909641 | ||||||
chr5:909672
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.866+1211A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909672 | ||||||
chr5:909706
|
T | A | 1 | a0001c0001t0002g0018 | 4 | HG02965.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+1245T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909706 | ||||||
chr5:909818
|
A | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0107 | 2 | HG00642.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.866+1357A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909818 | ||||||
chr5:909889
|
T | C | 1 | a0001c0001t0002g0028 | 3 | HG01081.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.866+1428T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909889 | ||||||
chr5:909991
|
G | GT | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.866+1532dupT | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 909991 | |||||
chr5:910155
|
C | T | 30 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0024others(27): Show | 59 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.867-1688C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910155 | ||||||
chr5:910165
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.867-1678C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910165 | ||||||
chr5:910166
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.867-1677G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910166 | ||||||
chr5:910300
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.867-1543C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910300 | ||||||
chr5:910356
|
G | T | 1 | a0002c0004t0001g0053 | 2 | HG00673.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.867-1487G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910356 | ||||||
chr5:910530
|
G | A | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.867-1313G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910530 | ||||||
chr5:910663
|
C | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-1180C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910663 | ||||||
chr5:910665
|
C | T | 4 | a0001c0001t0002g0186a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 4 | HG02280.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.867-1178C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910665 | ||||||
chr5:910671
|
T | C | 15 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(12): Show | 32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.867-1172T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910671 | ||||||
chr5:910777
|
C | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0075 | 4 | NA18950.hp2 NA19056.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.867-1066C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910777 | ||||||
chr5:910868
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.867-975G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910868 | ||||||
chr5:910911
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.867-932C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910911 | ||||||
chr5:910926
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.867-917G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910926 | ||||||
chr5:911061
|
C | T | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-782C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911061 | ||||||
chr5:911115
|
C | T | 2 | a0001c0005t0002g0213a0001c0005t0002g0214 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.867-728C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911115 | ||||||
chr5:911121
|
C | T | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.867-722C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911121 | ||||||
chr5:911247
|
G | A | 8 | a0001c0001t0002g0025a0001c0001t0002g0152a0001c0001t0002g0153others(5): Show | 8 | HG02572.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.867-596G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911247 | ||||||
chr5:911260
|
G | A | 4 | a0001c0001t0002g0018a0001c0001t0002g0054a0001c0005t0002g0213others(1): Show | 8 | HG01243.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.867-583G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911260 | ||||||
chr5:911270
|
C | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01106.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.867-573C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911270 | ||||||
chr5:911270
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.867-573C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911270 | ||||||
chr5:911272
|
A | T | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0059others(2): Show | 11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.867-571A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911272 | ||||||
chr5:911276
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.867-567T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911276 | ||||||
chr5:911291
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.867-552G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911291 | ||||||
chr5:911346
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.867-497C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911346 | ||||||
chr5:911396
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.867-447C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911396 | ||||||
chr5:911408
|
A | G | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.867-435A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911408 | ||||||
chr5:911433
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.867-410C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911433 | ||||||
chr5:911444
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.867-399G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911444 | ||||||
chr5:911519
|
C | T | 1 | a0001c0001t0007g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.867-324C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911519 | ||||||
chr5:911561
|
ACT | A | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-279_867-278del others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 911561 | |||||
chr5:911579
|
A | T | 1 | a0001c0001t0002g0140 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.867-264A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911579 | ||||||
chr5:911644
|
T | TAGG | 7 | a0001c0001t0002g0018a0001c0001t0002g0028a0001c0001t0002g0054others(4): Show | 17 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.867-197_867-196ins others(3): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 911644 | |||||
chr5:911687
|
G | A | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.867-156G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911687 | ||||||
chr5:911696
|
G | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(39): Show | 61 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.867-147G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911696 | ||||||
chr5:911793
|
G | C | 1 | a0001c0001t0001g0166 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.867-50G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911793 | ||||||
chr5:912005
|
AT | A | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+19delT | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 912005 | |||||
chr5:912078
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1020+82C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912078 | ||||||
chr5:912269
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1020+273G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912269 | ||||||
chr5:912282
|
T | G | 1 | a0001c0001t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1020+286T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912282 | ||||||
chr5:912343
|
C | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1020+347C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912343 | ||||||
chr5:912419
|
A | G | 22 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0014others(19): Show | 46 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.1020+423A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912419 | ||||||
chr5:912438
|
T | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0079others(2): Show | 14 | HG00544.hp2 HG01943.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.1020+442T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912438 | ||||||
chr5:912474
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0096others(1): Show | 6 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+478G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912474 | ||||||
chr5:912487
|
C | T | 3 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058 | 3 | HG02280.hp2 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1020+491C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912487 | ||||||
chr5:912520
|
C | T | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+524C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912520 | ||||||
chr5:912553
|
CGT | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0060others(1): Show | 10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+563_1020+564d others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 912553 | |||||
chr5:912603
|
G | A | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+607G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912603 | ||||||
chr5:912640
|
CAT | C | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+645_1020+646d others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912640 | ||||||
chr5:912776
|
G | T | 1 | a0001c0001t0001g0020 | 3 | HG02109.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1020+780G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912776 | ||||||
chr5:912800
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1020+804T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912800 | ||||||
chr5:913156
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1020+1160C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913156 | ||||||
chr5:913205
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1020+1209G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913205 | ||||||
chr5:913226
|
T | C | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1020+1230T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913226 | ||||||
chr5:913241
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1021-1224T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913241 | ||||||
chr5:913250
|
G | C | 1 | a0001c0001t0002g0131 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1021-1215G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913250 | ||||||
chr5:913354
|
TTTTG | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0054 | 6 | HG02486.hp2 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021-1099_1021-109 others(8): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 913354 | |||||
chr5:913547
|
G | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(39): Show | 61 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.1021-918G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913547 | ||||||
chr5:913896
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1021-569C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913896 | ||||||
chr5:913938
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0029a0001c0001t0002g0149others(2): Show | 12 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021-527C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913938 | ||||||
chr5:913976
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1021-489G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913976 | ||||||
chr5:913983
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1021-482G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913983 | ||||||
chr5:913989
|
TCAGA | T | 6 | a0001c0001t0002g0018a0001c0001t0002g0028a0001c0001t0002g0054others(3): Show | 13 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1021-473_1021-470d others(6): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 913989 | |||||
chr5:914194
|
C | T | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-271C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914194 | ||||||
chr5:914209
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021-256G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914209 | ||||||
chr5:914241
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1021-224C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914241 | ||||||
chr5:914278
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0111 | 2 | HG00323.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1021-187G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914278 | ||||||
chr5:914340
|
G | A | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-125G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914340 | ||||||
chr5:914660
|
C | G | 1 | a0001c0001t0001g0198 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1133+83C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914660 | ||||||
chr5:914720
|
C | CGT | 45 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0073others(42): Show | 76 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1133+163_1133+164d others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 914720 | |||||
chr5:914720
|
C | CGTGT | 12 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0018others(9): Show | 31 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1133+161_1133+164d others(6): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 914720 | |||||
chr5:914720
|
CGT | C | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133+163_1133+164d others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 914720 | |||||
chr5:914720
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1133+155_1133+164d others(12): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 914720 | |||||
chr5:914759
|
G | A | 1 | a0001c0001t0001g0044 | 2 | NA18962.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1133+182G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914759 | ||||||
chr5:914820
|
C | CGT | 15 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(12): Show | 32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1133+243_1133+244i others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914820 | ||||||
chr5:914821
|
A | G | 15 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(12): Show | 32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1133+244A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914821 | ||||||
chr5:914908
|
G | A | 9 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(6): Show | 23 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1133+331G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914908 | ||||||
chr5:915025
|
G | T | 1 | a0001c0001t0001g0175 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1133+448G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915025 | ||||||
chr5:915050
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1133+473G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915050 | ||||||
chr5:915082
|
G | A | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0059others(2): Show | 11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1133+505G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915082 | ||||||
chr5:915310
|
C | A | 1 | a0001c0001t0002g0212 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1134-594C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915310 | ||||||
chr5:915310
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1134-594C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915310 | ||||||
chr5:915367
|
A | G | 5 | a0001c0001t0002g0025a0001c0001t0002g0155a0003c0003t0002g0025others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134-537A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915367 | ||||||
chr5:915397
|
GGGCAGGT others(49): Show |
G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134-494_1134-439d others(58): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 915397 | |||||
chr5:915410
|
C | A | 9 | a0001c0001t0002g0007a0001c0001t0002g0028a0001c0001t0002g0029others(6): Show | 19 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1134-494C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915410 | ||||||
chr5:915453
|
A | AGGCAGGT others(49): Show |
1 | a0001c0001t0001g0092 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1134-382_1134-327d others(58): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 915453 | |||||
chr5:915453
|
A | G | 16 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0014others(13): Show | 36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.1134-451A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915453 | ||||||
chr5:915466
|
A | C | 11 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(8): Show | 25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1134-438A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915466 | ||||||
chr5:915488
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1134-416G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915488 | ||||||
chr5:915522
|
A | C | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134-382A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915522 | ||||||
chr5:915534
|
C | A | 1 | a0001c0001t0002g0137 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1134-370C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915534 | ||||||
chr5:915562
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1134-342C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915562 | ||||||
chr5:915564
|
C | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0128 | 3 | NA18948.hp2 NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1134-340C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915564 | ||||||
chr5:915589
|
A | G | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1134-315A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915589 | ||||||
chr5:915712
|
C | T | 1 | a0001c0001t0001g0022 | 3 | NA18977.hp1 NA19057.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1134-192C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915712 | ||||||
chr5:915792
|
T | C | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1134-112T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915792 | ||||||
chr5:915828
|
G | A | 6 | a0001c0001t0002g0018a0001c0001t0002g0028a0001c0001t0002g0054others(3): Show | 13 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1134-76G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915828 | ||||||
chr5:915843
|
T | C | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1134-61T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915843 | ||||||
chr5:915878
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1134-26C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915878 | ||||||
chr5:916027
|
C | T | 1 | a0001c0005t0002g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1203+54C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916027 | ||||||
chr5:916055
|
G | A | 2 | a0001c0001t0002g0136a0001c0001t0002g0138 | 2 | HG00408.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.1203+82G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916055 | ||||||
chr5:916167
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1203+194G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916167 | ||||||
chr5:916220
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1203+247G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916220 | ||||||
chr5:916362
|
T | C | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1203+389T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916362 | ||||||
chr5:916368
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0151 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1203+395G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916368 | ||||||
chr5:916372
|
T | C | 36 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0013others(33): Show | 65 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.1203+399T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916372 | ||||||
chr5:916373
|
G | T | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1203+400G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916373 | ||||||
chr5:916617
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 5 | HG01099.hp1 HG01891.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1204-391G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916617 | ||||||
chr5:916775
|
T | G | 12 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0028others(9): Show | 29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1204-233T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916775 | ||||||
chr5:916791
|
GC | G | 7 | a0001c0001t0002g0007a0001c0001t0002g0029a0001c0001t0002g0042others(4): Show | 18 | HG01175.hp2 HG01433.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1204-216delC | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916791 | ||||||
chr5:916792
|
C | G | 9 | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0002g0014others(6): Show | 20 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1204-216C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916792 | ||||||
chr5:916860
|
G | A | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-148G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916860 | ||||||
chr5:916991
|
G | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0043others(38): Show | 60 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.1204-17G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916991 | ||||||
chr5:916995
|
G | A | 13 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0002g0007others(10): Show | 27 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1204-13G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916995 |