geneid | 167153 |
---|---|
ensemblid | ENSG00000164329.15 |
hgncid | 26776 |
symbol | TENT2 |
name | terminal nucleotidyltransferase 2 |
refseq_nuc | NM_001114394.3 |
refseq_prot | NP_001107866.1 |
ensembl_nuc | ENST00000453514.6 |
ensembl_prot | ENSP00000397563.1 |
mane_status | MANE Select |
chr | chr5 |
start | 79612441 |
end | 79688246 |
strand | + |
ver | v1.2 |
region | chr5:79612441-79688246 |
region5000 | chr5:79607441-79693246 |
regionname0 | TENT2_chr5_79612441_79688246 |
regionname5000 | TENT2_chr5_79607441_79693246 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 484 | 340 | 87 | 50 | 149 | 12 | 40 | 113 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0002 | 0/0 | 484 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0003 | 0/0 | 484 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0004 | 0/0 | 484 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1455 | 317 | 85 | 40 | 143 | 12 | 35 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
c0002 | 0/0 | 1455 | 18 | 1 | 10 | 2 | 0 | 5 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
c0003 | 0/0 | 1455 | 4 | 0 | 0 | 4 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
c0004 | 0/0 | 1455 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
c0005 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
c0006 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
c0007 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3649 | 146 | 21 | 22 | 87 | 4 | 12 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0002 | 0/0 | 3647 | 33 | 1 | 10 | 18 | 0 | 4 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0003 | 0/0 | 3644 | 24 | 5 | 1 | 11 | 0 | 7 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0004 | 0/0 | 3647 | 22 | 22 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0005 | 0/0 | 3649 | 17 | 0 | 0 | 13 | 0 | 4 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0006 | 0/0 | 3652 | 16 | 3 | 4 | 5 | 2 | 2 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0007 | 0/0 | 3649 | 9 | 0 | 1 | 5 | 2 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0008 | 0/1 | 3649 | 8 | 0 | 0 | 5 | 0 | 2 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0009 | 0/0 | 3647 | 7 | 6 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0010 | 0/0 | 3644 | 6 | 0 | 0 | 4 | 2 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0011 | 0/0 | 3644 | 6 | 5 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0012 | 0/0 | 3647 | 3 | 3 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0013 | 0/0 | 3649 | 3 | 1 | 1 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0014 | 0/0 | 3652 | 3 | 0 | 0 | 1 | 1 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0015 | 0/0 | 3652 | 3 | 0 | 3 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0016 | 0/0 | 3647 | 2 | 1 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0017 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0018 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0019 | 0/0 | 3649 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0020 | 0/0 | 3649 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0021 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0022 | 0/0 | 3644 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0023 | 0/0 | 3644 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0024 | 0/0 | 3644 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0025 | 0/0 | 3647 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0026 | 0/0 | 3647 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0027 | 0/0 | 3644 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0028 | 0/0 | 3649 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0029 | 0/0 | 3649 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0030 | 0/0 | 3649 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0031 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0032 | 0/0 | 3649 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0033 | 0/0 | 3649 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0034 | 1/0 | 3646 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0035 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0036 | 0/0 | 3652 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0037 | 0/0 | 3652 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0038 | 0/0 | 3649 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0039 | 0/0 | 3652 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0040 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0041 | 0/0 | 3649 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0042 | 0/0 | 3649 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0043 | 0/0 | 3646 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0044 | 0/0 | 3652 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0045 | 0/0 | 3649 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0046 | 0/0 | 3649 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
t0047 | 0/0 | 3649 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1455 | 317 | 85 | 40 | 143 | 12 | 35 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0002 | 0/0 | 1455 | 18 | 1 | 10 | 2 | 0 | 5 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0003 | 0/0 | 1455 | 4 | 0 | 0 | 4 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0007 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0002c0004 | 0/0 | 1455 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0003c0005 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0004c0006 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5103 | 146 | 21 | 22 | 87 | 4 | 12 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0002 | 0/0 | 5101 | 20 | 1 | 0 | 18 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0003 | 0/0 | 5098 | 19 | 5 | 1 | 6 | 0 | 7 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0004 | 0/0 | 5101 | 21 | 21 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0005 | 0/0 | 5103 | 17 | 0 | 0 | 13 | 0 | 4 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0006 | 0/0 | 5106 | 16 | 3 | 4 | 5 | 2 | 2 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0007 | 0/0 | 5103 | 9 | 0 | 1 | 5 | 2 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0008 | 0/1 | 5103 | 8 | 0 | 0 | 5 | 0 | 2 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0009 | 0/0 | 5101 | 7 | 6 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0010 | 0/0 | 5098 | 2 | 0 | 0 | 0 | 2 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0011 | 0/0 | 5098 | 6 | 5 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0012 | 0/0 | 5101 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0013 | 0/0 | 5103 | 3 | 1 | 1 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0014 | 0/0 | 5106 | 3 | 0 | 0 | 1 | 1 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0015 | 0/0 | 5106 | 3 | 0 | 3 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0016 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0017 | 0/0 | 5106 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0018 | 0/0 | 5106 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0019 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0020 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0021 | 0/0 | 5106 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0022 | 0/0 | 5098 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0024 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0026 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0027 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0028 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0029 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0030 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0031 | 0/0 | 5106 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0032 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0033 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0034 | 1/0 | 5100 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0035 | 0/0 | 5106 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0036 | 0/0 | 5106 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0037 | 0/0 | 5106 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0038 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0039 | 0/0 | 5106 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0040 | 0/0 | 5106 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0041 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0042 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0043 | 0/0 | 5100 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0044 | 0/0 | 5106 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0045 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0046 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0001t0047 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0002t0002 | 0/0 | 5101 | 13 | 0 | 10 | 0 | 0 | 3 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0002t0003 | 0/0 | 5098 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0002t0012 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0002t0016 | 0/0 | 5101 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0002t0023 | 0/0 | 5098 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0003t0010 | 0/0 | 5098 | 4 | 0 | 0 | 4 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0001c0007t0025 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0002c0004t0003 | 0/0 | 5098 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0003c0005t0004 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
a0004c0006t0003 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | copy fasta | chr5 | 79607441 | 79693246 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0007g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0007g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0008g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0008g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0008g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0008g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0010g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0011g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0011g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0013g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0013g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0013g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0014g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0014g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0014g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0015g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0015g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0015g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0016g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0017g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0017g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0018g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0018g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0019g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0019g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0020g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0020g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0021g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0021g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0022g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0024g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0026g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0027g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0028g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0029g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0030g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0031g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0032g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0033g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0034g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0035g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0036g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0037g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0038g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0039g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0040g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0041g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0042g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0043g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0044g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0045g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0046g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0001t0047g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0016g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0002t0023g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0003t0010g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0003t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0003t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0003t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0001c0007t0025g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0002c0004t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0002c0004t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0003c0005t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
a0004c0006t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0014 | g0118 | EUR | GBR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0303 | EUR | GBR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00140 | hp1 | a0001 | c0001 | t0033 | g0234 | EUR | GBR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | GBR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00280 | hp1 | a0001 | c0001 | t0007 | g0199 | EUR | FIN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00408 | hp2 | a0001 | c0001 | t0008 | g0180 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00423 | hp2 | a0001 | c0001 | t0014 | g0150 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00544 | hp2 | a0001 | c0002 | t0003 | g0048 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00558 | hp2 | a0001 | c0001 | t0032 | g0242 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0128 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0099 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0315 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01167 | hp1 | a0001 | c0001 | t0043 | g0243 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01167 | hp2 | a0001 | c0001 | t0022 | g0078 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0237 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01243 | hp2 | a0001 | c0001 | t0045 | g0005 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01255 | hp2 | a0001 | c0001 | t0013 | g0224 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01257 | hp1 | a0001 | c0001 | t0015 | g0300 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01358 | hp2 | a0001 | c0001 | t0039 | g0282 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0049 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0227 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01515 | hp2 | a0001 | c0001 | t0010 | g0002 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0340 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01517 | hp2 | a0001 | c0001 | t0010 | g0002 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01884 | hp1 | a0001 | c0007 | t0025 | g0107 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0028 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01943 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0050 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0031 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01978 | hp2 | a0001 | c0001 | t0028 | g0331 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01981 | hp1 | a0001 | c0001 | t0030 | g0186 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02004 | hp2 | a0001 | c0001 | t0044 | g0297 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02040 | hp2 | a0001 | c0001 | t0005 | g0111 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0208 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0124 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0084 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CDX | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CDX | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0293 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02273 | hp2 | a0001 | c0001 | t0015 | g0302 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02280 | hp2 | a0001 | c0001 | t0016 | g0030 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02293 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0052 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02300 | hp1 | a0001 | c0001 | t0015 | g0296 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02451 | hp1 | a0001 | c0001 | t0018 | g0258 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02572 | hp2 | a0003 | c0005 | t0004 | g0074 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0127 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0077 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02615 | hp2 | a0001 | c0001 | t0018 | g0137 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0083 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02622 | hp2 | a0001 | c0001 | t0020 | g0133 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02647 | hp1 | a0001 | c0001 | t0041 | g0110 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02683 | hp2 | a0001 | c0001 | t0013 | g0245 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02717 | hp1 | a0001 | c0001 | t0019 | g0132 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02717 | hp2 | a0001 | c0001 | t0021 | g0113 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02738 | hp1 | a0001 | c0002 | t0023 | g0106 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02738 | hp2 | a0001 | c0001 | t0036 | g0109 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02809 | hp1 | a0001 | c0001 | t0027 | g0075 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02818 | hp1 | a0001 | c0001 | t0017 | g0136 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02818 | hp2 | a0001 | c0001 | t0040 | g0144 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02886 | hp1 | a0001 | c0002 | t0012 | g0097 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0290 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0291 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02965 | hp2 | a0001 | c0001 | t0024 | g0023 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02970 | hp2 | a0001 | c0001 | t0038 | g0226 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0098 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0149 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0330 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03098 | hp2 | a0001 | c0001 | t0042 | g0339 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0104 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03195 | hp1 | a0001 | c0001 | t0017 | g0142 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03225 | hp1 | a0001 | c0001 | t0031 | g0257 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03239 | hp1 | a0001 | c0001 | t0029 | g0249 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03239 | hp2 | a0001 | c0002 | t0016 | g0108 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03453 | hp1 | a0001 | c0001 | t0020 | g0130 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0126 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0103 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03579 | hp1 | a0001 | c0001 | t0019 | g0131 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0066 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03688 | hp1 | a0001 | c0001 | t0014 | g0119 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0102 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03704 | hp2 | a0001 | c0001 | t0006 | g0277 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03710 | hp1 | a0001 | c0001 | t0009 | g0032 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0146 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0319 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03927 | hp1 | a0001 | c0001 | t0037 | g0148 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0194 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0333 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18747 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | CHB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0091 | AFR | YRI | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | YRI | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18941 | hp2 | a0002 | c0004 | t0003 | g0054 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18947 | hp1 | a0001 | c0001 | t0046 | g0064 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18947 | hp2 | a0001 | c0003 | t0010 | g0089 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18951 | hp2 | a0002 | c0004 | t0003 | g0040 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0197 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18962 | hp2 | a0001 | c0003 | t0010 | g0037 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18964 | hp1 | a0001 | c0001 | t0007 | g0218 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18965 | hp2 | a0001 | c0001 | t0008 | g0263 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18971 | hp2 | a0001 | c0001 | t0047 | g0246 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18972 | hp2 | a0001 | c0001 | t0007 | g0196 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18977 | hp1 | a0001 | c0001 | t0008 | g0324 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18979 | hp2 | a0001 | c0001 | t0008 | g0267 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18980 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18983 | hp1 | a0001 | c0001 | t0006 | g0289 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18984 | hp2 | a0001 | c0001 | t0007 | g0121 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18994 | hp2 | a0001 | c0001 | t0007 | g0198 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18995 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18999 | hp2 | a0001 | c0001 | t0008 | g0210 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19000 | hp1 | a0001 | c0003 | t0010 | g0094 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19006 | hp1 | a0001 | c0001 | t0006 | g0262 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0322 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19010 | hp2 | a0001 | c0003 | t0010 | g0093 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19043 | hp1 | a0001 | c0001 | t0026 | g0069 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19070 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19074 | hp2 | a0004 | c0006 | t0003 | g0134 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19080 | hp1 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19087 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19088 | hp2 | a0001 | c0001 | t0006 | g0275 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | YRI | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0027 | AFR | YRI | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ASW | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA20129 | hp2 | a0001 | c0001 | t0012 | g0105 | AFR | ASW | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | GIH | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0288 | SAS | GIH | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02486 | hp2 | a0001 | c0001 | t0021 | g0112 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA20300 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | USA | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA21309 | hp1 | a0001 | c0001 | t0035 | g0143 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0247 | REF | REF | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0034 | g0250 | REF | REF | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:79619674
|
G | A | 1 | a0002 | 2 | NA18941.hp2 NA18951.hp2 |
missense_variant | MODERATE | c.26G>A | p.Arg9His | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/15 | 698/5100 | 26/1455 | 9/484 | chr5 | 79619674 | ||
chr5:79619770
|
A | G | 1 | a0004 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.122A>G | p.Asn41Ser | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/15 | 794/5100 | 122/1455 | 41/484 | chr5 | 79619770 | ||
chr5:79685205
|
C | T | 1 | a0003 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1387C>T | p.His463Tyr | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2059/5100 | 1387/1455 | 463/484 | chr5 | 79685205 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:79619744
|
C | T | 1 | a0001c0007 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.96C>T | p.His32His | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/15 | 768/5100 | 96/1455 | 32/484 | chr5 | 79619744 | ||
chr5:79668906
|
T | G | 1 | a0001c0002 | 18 | HG00544.hp2 HG01433.hp2 HG01928.hp2 others(15): Show |
synonymous_variant | LOW | c.1086T>G | p.Pro362Pro | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/15 | 1758/5100 | 1086/1455 | 362/484 | chr5 | 79668906 | ||
chr5:79682016
|
G | A | 1 | a0001c0003 | 4 | NA18947.hp2 NA18962.hp2 NA19000.hp1 others(1): Show |
synonymous_variant | LOW | c.1335G>A | p.Val445Val | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/15 | 2007/5100 | 1335/1455 | 445/484 | chr5 | 79682016 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:79612460
|
T | C | 1 | a0001c0001t0022 | 1 | HG01167.hp2 | 5_prime_UTR_variant | MODIFIER | c.-653T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 7189 | chr5 | 79612460 | |||||
chr5:79612529
|
A | G | 1 | a0001c0001t0047 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-584A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 7120 | chr5 | 79612529 | |||||
chr5:79612702
|
C | G | 1 | a0001c0001t0046 | 1 | NA18947.hp1 | 5_prime_UTR_variant | MODIFIER | c.-411C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 6947 | chr5 | 79612702 | |||||
chr5:79612757
|
C | T | 1 | a0001c0001t0045 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-356C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 6892 | chr5 | 79612757 | |||||
chr5:79612901
|
C | T | 2 | a0001c0001t0015a0001c0001t0044 | 4 | HG01257.hp1 HG02004.hp2 HG02273.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-212C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 6748 | chr5 | 79612901 | |||||
chr5:79612981
|
C | T | 1 | a0001c0001t0043 | 1 | HG01167.hp1 | 5_prime_UTR_variant | MODIFIER | c.-132C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 6668 | chr5 | 79612981 | |||||
chr5:79685428
|
A | T | 1 | a0001c0001t0021 | 2 | HG02486.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*155A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 155 | chr5 | 79685428 | |||||
chr5:79685546
|
TAACTG | T | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*277_*281delTGAAC | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 277 | INFO_REALIGN_3_PRIME | chr5 | 79685546 | ||||
chr5:79685606
|
T | G | 1 | a0001c0002t0023 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 333 | chr5 | 79685606 | |||||
chr5:79685727
|
G | T | 35 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(32): Show | 151 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*454G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 454 | chr5 | 79685727 | |||||
chr5:79686102
|
A | G | 1 | a0001c0001t0036 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*829A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 829 | chr5 | 79686102 | |||||
chr5:79686296
|
A | C | 1 | a0001c0001t0042 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1023A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1023 | chr5 | 79686296 | |||||
chr5:79686365
|
T | G | 9 | a0001c0001t0005a0001c0001t0007a0001c0001t0014others(6): Show | 37 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1092T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1092 | chr5 | 79686365 | |||||
chr5:79686740
|
C | A | 2 | a0001c0001t0019a0001c0001t0020 | 4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1467C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1467 | chr5 | 79686740 | |||||
chr5:79686869
|
A | G | 1 | a0001c0001t0035 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1596A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1596 | chr5 | 79686869 | |||||
chr5:79686962
|
T | C | 2 | a0001c0001t0019a0001c0001t0020 | 4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1689T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1689 | chr5 | 79686962 | |||||
chr5:79687096
|
T | C | 1 | a0001c0001t0029 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1823T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1823 | chr5 | 79687096 | |||||
chr5:79687133
|
G | GCTT | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*1861_*1863dupCTT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1864 | INFO_REALIGN_3_PRIME | chr5 | 79687133 | ||||
chr5:79687295
|
T | C | 1 | a0001c0001t0024 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2022T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2022 | chr5 | 79687295 | |||||
chr5:79687555
|
A | G | 1 | a0001c0001t0033 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2282 | chr5 | 79687555 | |||||
chr5:79687594
|
A | G | 10 | a0001c0001t0011a0001c0001t0012a0001c0001t0013others(7): Show | 19 | HG01109.hp1 HG01243.hp2 HG01255.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2321A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2321 | chr5 | 79687594 | |||||
chr5:79687614
|
C | T | 1 | a0001c0001t0037 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2341C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2341 | chr5 | 79687614 | |||||
chr5:79687690
|
A | G | 7 | a0001c0001t0005a0001c0001t0008a0001c0001t0010others(4): Show | 34 | HG00408.hp2 HG00558.hp1 HG01515.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2417A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2417 | chr5 | 79687690 | |||||
chr5:79687705
|
C | T | 1 | a0001c0001t0032 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2432C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2432 | chr5 | 79687705 | |||||
chr5:79687775
|
A | C | 11 | a0001c0001t0004a0001c0001t0009a0001c0001t0016others(8): Show | 40 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2502A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2502 | chr5 | 79687775 | |||||
chr5:79687876
|
G | A | 1 | a0001c0001t0044 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2603G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2603 | chr5 | 79687876 | |||||
chr5:79687877
|
C | A | 1 | a0001c0007t0025 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2604C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2604 | chr5 | 79687877 | |||||
chr5:79687995
|
G | GAAT | 24 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(21): Show | 104 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2725_*2727dupTAA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2728 | INFO_REALIGN_3_PRIME | chr5 | 79687995 | ||||
chr5:79688036
|
G | A | 1 | a0001c0001t0030 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2763G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2763 | chr5 | 79688036 | |||||
chr5:79688130
|
A | G | 1 | a0001c0001t0031 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2857A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2857 | chr5 | 79688130 | |||||
chr5:79688223
|
A | G | 11 | a0001c0001t0004a0001c0001t0016a0001c0001t0018others(8): Show | 33 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2950A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2950 | chr5 | 79688223 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:79613140
|
A | G | 1 | a0001c0001t0006g0340 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-38+65A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79613140 | ||||||
chr5:79613501
|
T | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+426T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79613501 | ||||||
chr5:79613703
|
C | T | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+628C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79613703 | ||||||
chr5:79614091
|
C | CT | 34 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(31): Show | 34 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.-38+1043dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | |||||
chr5:79614091
|
CT | C | 18 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(15): Show | 18 | HG01175.hp2 HG01433.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-38+1043delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | |||||
chr5:79614091
|
CTT | C | 94 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(91): Show | 94 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-38+1042_-38+1043d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | |||||
chr5:79614091
|
CTTT | C | 101 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(98): Show | 104 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-38+1041_-38+1043d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | |||||
chr5:79614091
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0041g0110a0001c0001t0045g0005 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-38+1034_-38+1043d others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | |||||
chr5:79614091
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0036g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-38+1031_-38+1043d others(15): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | |||||
chr5:79614119
|
G | T | 1 | a0001c0001t0001g0338 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-38+1044G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614119 | ||||||
chr5:79614135
|
A | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+1060A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614135 | ||||||
chr5:79614309
|
G | A | 35 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(32): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.-38+1234G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614309 | ||||||
chr5:79614425
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+1350C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614425 | ||||||
chr5:79614704
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-38+1629G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614704 | ||||||
chr5:79614780
|
A | T | 1 | a0001c0001t0016g0030 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-38+1705A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614780 | ||||||
chr5:79614808
|
TTA | T | 4 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+1735_-38+1736d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614808 | |||||
chr5:79614952
|
G | A | 1 | a0001c0001t0003g0006 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-38+1877G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614952 | ||||||
chr5:79615253
|
C | T | 1 | a0001c0002t0023g0106 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-38+2178C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615253 | ||||||
chr5:79615370
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+2295G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615370 | ||||||
chr5:79615486
|
A | G | 1 | a0001c0001t0003g0006 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-38+2411A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615486 | ||||||
chr5:79615549
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-38+2474C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615549 | ||||||
chr5:79615641
|
G | A | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+2566G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615641 | ||||||
chr5:79615709
|
C | CT | 104 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(101): Show | 106 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(103): Show |
intron_variant | MODIFIER | c.-38+2646dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79615709 | |||||
chr5:79615788
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-38+2713C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615788 | ||||||
chr5:79615807
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-38+2732G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615807 | ||||||
chr5:79615815
|
C | T | 1 | a0001c0001t0005g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-38+2740C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615815 | ||||||
chr5:79615991
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-38+2916C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615991 | ||||||
chr5:79616003
|
C | G | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-38+2928C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616003 | ||||||
chr5:79616008
|
C | T | 5 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(2): Show | 5 | HG00280.hp1 NA18960.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+2933C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616008 | ||||||
chr5:79616067
|
A | G | 1 | a0001c0001t0006g0303 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-38+2992A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616067 | ||||||
chr5:79616076
|
G | A | 59 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(56): Show | 61 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-38+3001G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616076 | ||||||
chr5:79616077
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-38+3002G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616077 | ||||||
chr5:79616121
|
A | G | 1 | a0001c0001t0001g0336 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-38+3046A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616121 | ||||||
chr5:79616140
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-38+3065G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616140 | ||||||
chr5:79616152
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0220a0001c0001t0017g0136 | 3 | HG02630.hp1 HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38+3077G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616152 | ||||||
chr5:79616189
|
A | AT | 29 | a0001c0001t0001g0195a0001c0001t0001g0201a0001c0001t0001g0217others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.-38+3140dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616189 | |||||
chr5:79616189
|
AT | A | 15 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(12): Show | 15 | HG01074.hp2 HG01255.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+3140delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616189 | |||||
chr5:79616189
|
ATT | A | 8 | a0001c0001t0002g0067a0001c0001t0004g0029a0001c0001t0004g0085others(5): Show | 8 | HG01934.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-38+3139_-38+3140d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616189 | |||||
chr5:79616189
|
ATTT | A | 98 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(95): Show | 101 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.-38+3138_-38+3140d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616189 | |||||
chr5:79616262
|
G | A | 1 | a0001c0001t0018g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-38+3187G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616262 | ||||||
chr5:79616285
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+3210G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616285 | ||||||
chr5:79616474
|
C | T | 3 | a0001c0002t0002g0066a0001c0002t0002g0102a0001c0002t0023g0106 | 3 | HG02738.hp1 HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-37-3138C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616474 | ||||||
chr5:79616475
|
G | A | 1 | a0001c0001t0005g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-37-3137G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616475 | ||||||
chr5:79616557
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-3055A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616557 | ||||||
chr5:79616671
|
T | TTG | 213 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(210): Show | 216 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.-37-2940_-37-2939i others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616671 | |||||
chr5:79616779
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-37-2833T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616779 | ||||||
chr5:79616889
|
A | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-2723A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616889 | ||||||
chr5:79616916
|
A | G | 2 | a0001c0001t0004g0001a0001c0001t0016g0030 | 3 | HG02280.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-37-2696A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616916 | ||||||
chr5:79616970
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-2642A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616970 | ||||||
chr5:79616973
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-37-2639G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616973 | ||||||
chr5:79617016
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-37-2596C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617016 | ||||||
chr5:79617017
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-37-2595T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617017 | ||||||
chr5:79617018
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-37-2594C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617018 | ||||||
chr5:79617020
|
C | T | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.-37-2592C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617020 | ||||||
chr5:79617060
|
A | G | 1 | a0001c0001t0005g0125 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-37-2552A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617060 | ||||||
chr5:79617128
|
A | C | 8 | a0001c0001t0005g0120a0001c0001t0005g0122a0001c0001t0005g0123others(5): Show | 8 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-2484A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617128 | ||||||
chr5:79617482
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-37-2130A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617482 | ||||||
chr5:79617514
|
A | G | 3 | a0001c0001t0006g0290a0001c0001t0006g0291a0001c0001t0006g0330 | 3 | HG02886.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-37-2098A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617514 | ||||||
chr5:79617530
|
A | G | 1 | a0001c0001t0015g0302 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-37-2082A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617530 | ||||||
chr5:79617530
|
A | T | 1 | a0001c0001t0006g0289 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-37-2082A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617530 | ||||||
chr5:79617597
|
C | T | 12 | a0001c0001t0002g0076a0001c0001t0003g0070a0001c0001t0004g0071others(9): Show | 12 | HG01167.hp2 HG02486.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37-2015C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617597 | ||||||
chr5:79617618
|
G | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-1994G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617618 | ||||||
chr5:79617816
|
T | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-1796T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617816 | ||||||
chr5:79617926
|
T | C | 1 | a0001c0001t0045g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-37-1686T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617926 | ||||||
chr5:79618402
|
A | AT | 106 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(103): Show | 109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.-37-1198dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79618402 | |||||
chr5:79618412
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-37-1200T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618412 | ||||||
chr5:79618484
|
C | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-1128C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618484 | ||||||
chr5:79618524
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-1088A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618524 | ||||||
chr5:79618594
|
G | GT | 33 | a0001c0001t0001g0145a0001c0001t0001g0189a0001c0001t0001g0190others(30): Show | 33 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.-37-1008dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79618594 | |||||
chr5:79618728
|
G | A | 7 | a0001c0001t0001g0151a0001c0001t0019g0131a0001c0001t0019g0132others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-884G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618728 | ||||||
chr5:79618739
|
C | T | 1 | a0001c0001t0008g0288 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-37-873C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618739 | ||||||
chr5:79619050
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-562A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619050 | ||||||
chr5:79619082
|
C | G | 8 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0086others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-530C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619082 | ||||||
chr5:79619292
|
G | A | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-320G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619292 | ||||||
chr5:79619308
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-37-304G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619308 | ||||||
chr5:79619399
|
A | G | 1 | a0001c0001t0024g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-37-213A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619399 | ||||||
chr5:79619461
|
C | A | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-151C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619461 | ||||||
chr5:79619839
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0028g0331 | 2 | HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.137+54G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/14 | chr5 | 79619839 | ||||||
chr5:79619870
|
A | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0287a0001c0001t0001g0329 | 3 | HG01516.hp2 HG01517.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.137+85A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/14 | chr5 | 79619870 | ||||||
chr5:79620169
|
A | C | 61 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(58): Show | 61 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.227+86A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79620169 | ||||||
chr5:79620774
|
G | C | 1 | a0001c0001t0001g0307 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.227+691G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79620774 | ||||||
chr5:79620895
|
A | T | 1 | a0001c0001t0002g0065 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.227+812A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79620895 | ||||||
chr5:79620924
|
CAATT | C | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.227+846_227+849del others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79620924 | |||||
chr5:79621003
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.227+920C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621003 | ||||||
chr5:79621068
|
C | T | 1 | a0001c0001t0045g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.227+985C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621068 | ||||||
chr5:79621105
|
TA | T | 84 | a0001c0001t0001g0219a0001c0001t0001g0301a0001c0001t0002g0076others(81): Show | 85 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.227+1034delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79621105 | |||||
chr5:79621105
|
TAA | T | 58 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(55): Show | 60 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.227+1033_227+1034d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79621105 | |||||
chr5:79621578
|
G | A | 1 | a0001c0001t0005g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.227+1495G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621578 | ||||||
chr5:79621640
|
C | T | 1 | a0001c0001t0004g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.227+1557C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621640 | ||||||
chr5:79621757
|
C | CA | 15 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(12): Show | 15 | HG00099.hp2 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.228-1480dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79621757 | |||||
chr5:79621765
|
A | AC | 104 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(101): Show | 107 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.228-1487_228-1486i others(3): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621765 | ||||||
chr5:79621765
|
A | C | 1 | a0001c0001t0004g0085 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.228-1487A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621765 | ||||||
chr5:79621769
|
A | C | 106 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(103): Show | 109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.228-1483A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621769 | ||||||
chr5:79621776
|
A | AC | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-1476_228-1475i others(3): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621776 | ||||||
chr5:79621780
|
A | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-1472A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621780 | ||||||
chr5:79621782
|
C | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-1470C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621782 | ||||||
chr5:79621991
|
C | A | 3 | a0001c0001t0003g0008a0001c0001t0003g0079a0001c0001t0011g0007 | 3 | HG03139.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.228-1261C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621991 | ||||||
chr5:79622173
|
C | T | 2 | a0001c0001t0042g0339a0001c0001t0045g0005 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.228-1079C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622173 | ||||||
chr5:79622194
|
A | G | 1 | a0001c0001t0017g0142 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.228-1058A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622194 | ||||||
chr5:79622261
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-991C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622261 | ||||||
chr5:79622276
|
C | T | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.228-976C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622276 | ||||||
chr5:79622293
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-959T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622293 | ||||||
chr5:79622556
|
G | C | 4 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-696G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622556 | ||||||
chr5:79622622
|
G | C | 1 | a0001c0001t0041g0110 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.228-630G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622622 | ||||||
chr5:79622642
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-610C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622642 | ||||||
chr5:79622737
|
A | G | 1 | a0001c0002t0003g0033 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.228-515A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622737 | ||||||
chr5:79622772
|
G | A | 4 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-480G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622772 | ||||||
chr5:79622780
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.228-472A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622780 | ||||||
chr5:79622786
|
T | C | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-466T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622786 | ||||||
chr5:79623054
|
A | AT | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-190dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79623054 | |||||
chr5:79623054
|
AT | A | 4 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-190delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79623054 | |||||
chr5:79623602
|
A | G | 1 | a0001c0007t0025g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.465+113A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79623602 | ||||||
chr5:79623779
|
G | GA | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+302dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79623779 | |||||
chr5:79623947
|
C | T | 2 | a0001c0001t0007g0199a0001c0001t0007g0218 | 2 | HG00280.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.465+458C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79623947 | ||||||
chr5:79623993
|
A | T | 1 | a0001c0001t0001g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465+504A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79623993 | ||||||
chr5:79624254
|
G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0214others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+765G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624254 | ||||||
chr5:79624340
|
T | C | 1 | a0001c0001t0018g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.465+851T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624340 | ||||||
chr5:79624374
|
A | G | 5 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0326others(2): Show | 5 | NA18978.hp1 NA18995.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+885A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624374 | ||||||
chr5:79624380
|
G | C | 1 | a0001c0001t0006g0208 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.465+891G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624380 | ||||||
chr5:79624411
|
T | C | 8 | a0001c0001t0001g0139a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | NA18955.hp1 NA18965.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+922T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624411 | ||||||
chr5:79624427
|
T | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+938T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624427 | ||||||
chr5:79624449
|
A | C | 45 | a0001c0001t0001g0203a0001c0001t0001g0207a0001c0001t0001g0222others(42): Show | 46 | HG00408.hp1 HG01256.hp1 HG01258.hp1 others(43): Show |
intron_variant | MODIFIER | c.465+960A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624449 | ||||||
chr5:79624585
|
C | T | 2 | a0001c0001t0038g0226a0001c0001t0041g0110 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.465+1096C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624585 | ||||||
chr5:79624688
|
T | C | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+1199T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624688 | ||||||
chr5:79624701
|
C | T | 1 | a0001c0001t0046g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.465+1212C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624701 | ||||||
chr5:79624723
|
A | G | 1 | a0001c0001t0026g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.465+1234A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624723 | ||||||
chr5:79624729
|
A | T | 1 | a0001c0001t0001g0325 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.465+1240A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624729 | ||||||
chr5:79625224
|
T | C | 1 | a0001c0001t0002g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.465+1735T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79625224 | ||||||
chr5:79625550
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+2061C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79625550 | ||||||
chr5:79625636
|
A | G | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+2147A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79625636 | ||||||
chr5:79625834
|
GT | G | 106 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(103): Show | 109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.465+2358delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79625834 | |||||
chr5:79625946
|
C | T | 1 | a0001c0001t0036g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.465+2457C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79625946 | ||||||
chr5:79626072
|
C | CCACTTTG others(7): Show |
1 | a0001c0001t0003g0006 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.465+2596_465+2597i others(16): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626072 | |||||
chr5:79626120
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+2631C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626120 | ||||||
chr5:79626277
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465+2788C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626277 | ||||||
chr5:79626306
|
A | AT | 18 | a0001c0001t0001g0222a0001c0001t0001g0228a0001c0001t0001g0231others(15): Show | 18 | HG00639.hp2 HG02055.hp1 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.465+2836dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626306 | |||||
chr5:79626306
|
AT | A | 29 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.465+2836delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626306 | |||||
chr5:79626408
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.465+2919C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626408 | ||||||
chr5:79626489
|
A | G | 1 | a0001c0001t0045g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.465+3000A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626489 | ||||||
chr5:79626619
|
T | C | 2 | a0001c0001t0007g0196a0001c0001t0007g0198 | 2 | NA18972.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.465+3130T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626619 | ||||||
chr5:79626625
|
A | AT | 149 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(146): Show | 152 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.465+3152dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626625 | |||||
chr5:79626625
|
A | ATT | 62 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(59): Show | 62 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.465+3151_465+3152d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626625 | |||||
chr5:79626789
|
G | GTAATGCC others(2): Show |
107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+3300_465+3301i others(11): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626789 | ||||||
chr5:79626832
|
A | G | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+3343A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626832 | ||||||
chr5:79626835
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.465+3346G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626835 | ||||||
chr5:79627091
|
C | G | 3 | a0001c0001t0001g0304a0001c0001t0018g0258a0001c0001t0031g0257 | 3 | HG02451.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.465+3602C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627091 | ||||||
chr5:79627096
|
G | C | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.465+3607G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627096 | ||||||
chr5:79627129
|
C | CA | 50 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(47): Show | 50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.465+3655dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79627129 | |||||
chr5:79627129
|
C | CAA | 155 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0141others(152): Show | 158 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.465+3654_465+3655d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79627129 | |||||
chr5:79627129
|
C | CAAA | 11 | a0001c0001t0001g0140a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 11 | HG00597.hp2 HG01109.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.465+3653_465+3655d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79627129 | |||||
chr5:79627155
|
T | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+3666T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627155 | ||||||
chr5:79627221
|
G | C | 1 | a0001c0001t0004g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.465+3732G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627221 | ||||||
chr5:79627235
|
C | G | 1 | a0001c0002t0002g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.465+3746C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627235 | ||||||
chr5:79627268
|
GAACT | G | 3 | a0001c0001t0009g0027a0001c0001t0009g0028a0001c0001t0009g0084 | 3 | HG01891.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.465+3788_465+3791d others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79627268 | |||||
chr5:79627495
|
C | T | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+4006C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627495 | ||||||
chr5:79627507
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+4018C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627507 | ||||||
chr5:79627735
|
T | A | 1 | a0001c0001t0002g0060 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.465+4246T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627735 | ||||||
chr5:79627847
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.465+4358G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627847 | ||||||
chr5:79627895
|
C | T | 1 | a0001c0001t0035g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.465+4406C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627895 | ||||||
chr5:79627900
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+4411A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627900 | ||||||
chr5:79627955
|
A | G | 1 | a0001c0001t0018g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.465+4466A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627955 | ||||||
chr5:79628017
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+4528G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628017 | ||||||
chr5:79628189
|
C | T | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+4700C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628189 | ||||||
chr5:79628199
|
G | A | 59 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(56): Show | 61 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.465+4710G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628199 | ||||||
chr5:79628276
|
G | A | 1 | a0001c0001t0035g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.465+4787G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628276 | ||||||
chr5:79628465
|
C | T | 1 | a0001c0001t0014g0119 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.465+4976C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628465 | ||||||
chr5:79628490
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+5001T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628490 | ||||||
chr5:79628682
|
T | G | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+5193T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628682 | ||||||
chr5:79628780
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.465+5291A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628780 | ||||||
chr5:79628786
|
C | T | 1 | a0001c0001t0015g0300 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.465+5297C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628786 | ||||||
chr5:79629017
|
G | C | 1 | a0001c0001t0033g0234 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.465+5528G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629017 | ||||||
chr5:79629068
|
AG | A | 4 | a0001c0001t0004g0024a0001c0001t0009g0027a0001c0001t0009g0028others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+5581delG | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79629068 | |||||
chr5:79629482
|
A | G | 7 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0086others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.465+5993A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629482 | ||||||
chr5:79629543
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.465+6054A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629543 | ||||||
chr5:79629603
|
GGATCACG others(4319): Show |
G | 1 | a0001c0001t0001g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.465+6155_466-6882d others(2): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79629603 | |||||
chr5:79629688
|
G | A | 60 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(57): Show | 62 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.465+6199G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629688 | ||||||
chr5:79629817
|
ACT | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6331_465+6332d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79629817 | |||||
chr5:79629887
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6398G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629887 | ||||||
chr5:79629920
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6431A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629920 | ||||||
chr5:79629958
|
A | AC | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6473dupC | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79629958 | |||||
chr5:79630083
|
C | G | 72 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(69): Show | 74 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.465+6594C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630083 | ||||||
chr5:79630089
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.465+6600C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630089 | ||||||
chr5:79630130
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6641G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630130 | ||||||
chr5:79630201
|
G | C | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.465+6712G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630201 | ||||||
chr5:79630253
|
G | A | 4 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(1): Show | 4 | HG03654.hp2 HG03927.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+6764G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630253 | ||||||
chr5:79630365
|
G | A | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+6876G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630365 | ||||||
chr5:79630624
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.465+7135T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630624 | ||||||
chr5:79630739
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+7250A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630739 | ||||||
chr5:79630804
|
G | A | 3 | a0001c0001t0002g0076a0001c0001t0003g0070a0001c0001t0012g0103 | 3 | HG02486.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.465+7315G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630804 | ||||||
chr5:79630817
|
G | GT | 113 | a0001c0001t0001g0206a0001c0001t0001g0231a0001c0001t0001g0256others(110): Show | 115 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(112): Show |
intron_variant | MODIFIER | c.465+7344dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79630817 | |||||
chr5:79630817
|
G | GTT | 58 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(55): Show | 59 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.465+7343_465+7344d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79630817 | |||||
chr5:79630817
|
GT | G | 9 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(6): Show | 9 | HG02055.hp1 HG02132.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+7344delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79630817 | |||||
chr5:79631137
|
A | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+7648A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631137 | ||||||
chr5:79631144
|
A | G | 1 | a0001c0002t0002g0098 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.465+7655A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631144 | ||||||
chr5:79631162
|
C | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+7673C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631162 | ||||||
chr5:79631195
|
A | G | 4 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+7706A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631195 | ||||||
chr5:79631230
|
T | C | 1 | a0001c0001t0005g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.465+7741T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631230 | ||||||
chr5:79631260
|
G | C | 1 | a0001c0001t0001g0266 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.465+7771G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631260 | ||||||
chr5:79631335
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.465+7846G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631335 | ||||||
chr5:79631519
|
T | C | 2 | a0001c0001t0008g0263a0001c0001t0008g0267 | 2 | NA18965.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.465+8030T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631519 | ||||||
chr5:79631537
|
C | G | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+8048C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631537 | ||||||
chr5:79631567
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.465+8078G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631567 | ||||||
chr5:79631595
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+8106G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631595 | ||||||
chr5:79631657
|
G | T | 1 | a0001c0001t0001g0318 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.465+8168G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631657 | ||||||
chr5:79631818
|
A | G | 1 | a0001c0001t0007g0128 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.465+8329A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631818 | ||||||
chr5:79631837
|
G | A | 2 | a0001c0001t0005g0114a0001c0001t0005g0146 | 2 | HG03831.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.465+8348G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631837 | ||||||
chr5:79631884
|
TAGG | T | 4 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+8401_465+8403d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79631884 | |||||
chr5:79631927
|
C | T | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+8438C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631927 | ||||||
chr5:79631975
|
G | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+8486G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631975 | ||||||
chr5:79631986
|
C | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+8497C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631986 | ||||||
chr5:79632166
|
A | G | 8 | a0001c0001t0001g0139a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | NA18955.hp1 NA18965.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+8677A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632166 | ||||||
chr5:79632254
|
T | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-8597T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632254 | ||||||
chr5:79632274
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.466-8577A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632274 | ||||||
chr5:79632726
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0018g0137 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.466-8125G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632726 | ||||||
chr5:79632731
|
G | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-8120G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632731 | ||||||
chr5:79632753
|
G | GACTCT | 5 | a0001c0001t0002g0035a0001c0001t0002g0065a0001c0001t0002g0068others(2): Show | 5 | HG02165.hp1 NA18950.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-8097_466-8093d others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79632753 | |||||
chr5:79632801
|
C | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-8050C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632801 | ||||||
chr5:79632806
|
A | G | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.466-8045A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632806 | ||||||
chr5:79632926
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.466-7925C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632926 | ||||||
chr5:79632962
|
A | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7889A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632962 | ||||||
chr5:79633015
|
A | G | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-7836A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633015 | ||||||
chr5:79633090
|
T | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0310 | 2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.466-7761T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633090 | ||||||
chr5:79633093
|
A | G | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-7758A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633093 | ||||||
chr5:79633121
|
G | A | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.466-7730G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633121 | ||||||
chr5:79633122
|
G | A | 2 | a0001c0001t0003g0009a0001c0001t0003g0011 | 2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.466-7729G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633122 | ||||||
chr5:79633183
|
C | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7668C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633183 | ||||||
chr5:79633212
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7639T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633212 | ||||||
chr5:79633239
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7612A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633239 | ||||||
chr5:79633413
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7438C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633413 | ||||||
chr5:79633432
|
G | GT | 67 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(64): Show | 67 | HG00544.hp1 HG00609.hp1 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.466-7394dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | |||||
chr5:79633432
|
G | GTT | 9 | a0001c0001t0001g0255a0001c0001t0002g0060a0001c0001t0002g0076others(6): Show | 9 | HG00597.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.466-7395_466-7394d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | |||||
chr5:79633432
|
G | GTTT | 21 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.466-7396_466-7394d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | |||||
chr5:79633432
|
G | GTTTT | 9 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(6): Show | 9 | HG02080.hp1 HG02602.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.466-7397_466-7394d others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | |||||
chr5:79633432
|
GT | G | 8 | a0001c0001t0002g0036a0001c0001t0011g0026a0001c0001t0019g0131others(5): Show | 8 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.466-7394delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | |||||
chr5:79633458
|
G | A | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-7393G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633458 | ||||||
chr5:79633502
|
T | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7349T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633502 | ||||||
chr5:79633605
|
G | A | 1 | a0001c0001t0007g0197 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.466-7246G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633605 | ||||||
chr5:79633635
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.466-7216C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633635 | ||||||
chr5:79633721
|
G | GT | 18 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(15): Show | 18 | HG01109.hp2 HG01884.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.466-7112dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633721 | |||||
chr5:79633721
|
GTTTTTT | G | 106 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(103): Show | 109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.466-7117_466-7112d others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633721 | |||||
chr5:79633935
|
C | T | 2 | a0001c0001t0014g0118a0001c0001t0014g0119 | 2 | HG00099.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.466-6916C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633935 | ||||||
chr5:79633950
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.466-6901G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633950 | ||||||
chr5:79633953
|
A | T | 16 | a0001c0002t0002g0031a0001c0002t0002g0047a0001c0002t0002g0049others(13): Show | 16 | HG00544.hp2 HG01433.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.466-6898A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633953 | ||||||
chr5:79633997
|
C | CA | 29 | a0001c0001t0001g0138a0001c0001t0001g0152a0001c0001t0001g0162others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.466-6832dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633997 | |||||
chr5:79633997
|
CAAA | C | 9 | a0001c0001t0002g0035a0001c0001t0002g0060a0001c0001t0020g0133others(6): Show | 9 | HG02622.hp2 HG03669.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.466-6834_466-6832d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633997 | |||||
chr5:79633997
|
CAAAA | C | 97 | a0001c0001t0002g0034a0001c0001t0002g0036a0001c0001t0002g0038others(94): Show | 100 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(97): Show |
intron_variant | MODIFIER | c.466-6835_466-6832d others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633997 | |||||
chr5:79634041
|
C | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-6810C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634041 | ||||||
chr5:79634091
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.466-6760G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634091 | ||||||
chr5:79634092
|
C | A | 1 | a0001c0001t0002g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.466-6759C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634092 | ||||||
chr5:79634114
|
C | T | 1 | a0001c0001t0035g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.466-6737C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634114 | ||||||
chr5:79634137
|
A | G | 4 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-6714A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634137 | ||||||
chr5:79634154
|
C | CA | 21 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0212others(18): Show | 21 | HG00597.hp1 HG00639.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.466-6678dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79634154 | |||||
chr5:79634154
|
CA | C | 29 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0001g0336others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-6678delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79634154 | |||||
chr5:79634170
|
A | C | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-6681A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634170 | ||||||
chr5:79634210
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.466-6641T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634210 | ||||||
chr5:79634237
|
A | C | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-6614A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634237 | ||||||
chr5:79634248
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-6603T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634248 | ||||||
chr5:79634278
|
G | T | 1 | a0001c0001t0001g0254 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.466-6573G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634278 | ||||||
chr5:79634286
|
A | T | 1 | a0001c0001t0001g0337 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.466-6565A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634286 | ||||||
chr5:79634447
|
C | T | 1 | a0001c0001t0041g0110 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.466-6404C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634447 | ||||||
chr5:79634482
|
A | C | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.466-6369A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634482 | ||||||
chr5:79634618
|
T | C | 164 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(161): Show | 167 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.466-6233T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634618 | ||||||
chr5:79634715
|
A | G | 60 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(57): Show | 62 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.466-6136A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634715 | ||||||
chr5:79634735
|
ATAGCCTA others(34): Show |
A | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-6103_466-6063d others(43): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79634735 | |||||
chr5:79634839
|
A | G | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-6012A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634839 | ||||||
chr5:79634874
|
G | A | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-5977G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634874 | ||||||
chr5:79635058
|
G | A | 1 | a0001c0001t0045g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.466-5793G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635058 | ||||||
chr5:79635164
|
C | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-5687C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635164 | ||||||
chr5:79635215
|
G | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-5636G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635215 | ||||||
chr5:79635420
|
G | A | 5 | a0001c0001t0001g0222a0001c0001t0001g0270a0001c0001t0001g0284others(2): Show | 5 | NA18940.hp2 NA18952.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-5431G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635420 | ||||||
chr5:79635454
|
C | CA | 339 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(336): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.466-5396dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79635454 | |||||
chr5:79635624
|
G | A | 1 | a0001c0001t0005g0126 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.466-5227G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635624 | ||||||
chr5:79635636
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-5215C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635636 | ||||||
chr5:79635678
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.466-5173C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635678 | ||||||
chr5:79635689
|
A | G | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-5162A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635689 | ||||||
chr5:79635897
|
G | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-4954G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635897 | ||||||
chr5:79636061
|
G | C | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-4790G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636061 | ||||||
chr5:79636096
|
A | G | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.466-4755A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636096 | ||||||
chr5:79636099
|
C | CT | 339 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(336): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.466-4751dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79636099 | |||||
chr5:79636428
|
C | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0046a0001c0001t0002g0063others(1): Show | 4 | NA18945.hp2 NA18972.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-4423C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636428 | ||||||
chr5:79636628
|
A | G | 1 | a0001c0001t0012g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.466-4223A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636628 | ||||||
chr5:79636676
|
G | C | 20 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(17): Show | 21 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.466-4175G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636676 | ||||||
chr5:79636894
|
G | A | 1 | a0001c0001t0006g0208 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.466-3957G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636894 | ||||||
chr5:79637127
|
G | T | 2 | a0001c0001t0001g0138a0001c0001t0018g0137 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.466-3724G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637127 | ||||||
chr5:79637129
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.466-3722A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637129 | ||||||
chr5:79637229
|
C | CA | 29 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-3610dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637229 | |||||
chr5:79637229
|
CA | C | 58 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(55): Show | 58 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.466-3610delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637229 | |||||
chr5:79637229
|
CAA | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-3611_466-3610d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637229 | |||||
chr5:79637473
|
C | T | 1 | a0001c0001t0006g0340 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.466-3378C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637473 | ||||||
chr5:79637628
|
T | C | 14 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0001g0238others(11): Show | 14 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.466-3223T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637628 | ||||||
chr5:79637798
|
C | CT | 103 | a0001c0001t0001g0181a0001c0001t0001g0216a0001c0001t0001g0259others(100): Show | 106 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(103): Show |
intron_variant | MODIFIER | c.466-3036dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637798 | |||||
chr5:79637798
|
C | CTT | 8 | a0001c0001t0002g0063a0001c0001t0002g0067a0001c0001t0003g0045others(5): Show | 8 | HG02055.hp2 HG02273.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.466-3037_466-3036d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637798 | |||||
chr5:79637798
|
CT | C | 7 | a0001c0001t0002g0076a0001c0001t0003g0070a0001c0001t0004g0072others(4): Show | 7 | HG02486.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-3036delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637798 | |||||
chr5:79637814
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.466-3037T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637814 | ||||||
chr5:79637821
|
G | A | 30 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.466-3030G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637821 | ||||||
chr5:79637827
|
G | A | 1 | a0001c0001t0008g0288 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.466-3024G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637827 | ||||||
chr5:79637880
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0328 | 2 | NA19080.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.466-2971C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637880 | ||||||
chr5:79637923
|
A | G | 1 | a0001c0002t0002g0050 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.466-2928A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637923 | ||||||
chr5:79638044
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-2807T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638044 | ||||||
chr5:79638318
|
C | A | 14 | a0001c0001t0004g0010a0001c0001t0004g0014a0001c0001t0004g0015others(11): Show | 14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.466-2533C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638318 | ||||||
chr5:79638506
|
T | C | 1 | a0001c0001t0045g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.466-2345T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638506 | ||||||
chr5:79638733
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-2118C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638733 | ||||||
chr5:79638768
|
A | G | 1 | a0001c0001t0029g0249 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.466-2083A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638768 | ||||||
chr5:79638797
|
G | T | 7 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0086others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-2054G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638797 | ||||||
chr5:79638909
|
G | C | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.466-1942G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638909 | ||||||
chr5:79638990
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0200 | 2 | HG02074.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.466-1861G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638990 | ||||||
chr5:79639012
|
A | G | 1 | a0001c0002t0012g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.466-1839A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639012 | ||||||
chr5:79639047
|
T | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-1804T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639047 | ||||||
chr5:79639119
|
C | G | 1 | a0001c0001t0008g0180 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.466-1732C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639119 | ||||||
chr5:79639330
|
A | C | 1 | a0001c0001t0035g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.466-1521A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639330 | ||||||
chr5:79639374
|
G | T | 1 | a0001c0001t0001g0298 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.466-1477G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639374 | ||||||
chr5:79639477
|
G | GT | 18 | a0001c0001t0003g0070a0001c0001t0004g0071a0001c0001t0004g0072others(15): Show | 18 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.466-1362dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79639477 | |||||
chr5:79639477
|
G | GTT | 72 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(69): Show | 74 | HG00673.hp2 HG01515.hp2 HG01517.hp2 others(71): Show |
intron_variant | MODIFIER | c.466-1363_466-1362d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79639477 | |||||
chr5:79639477
|
G | GTTT | 22 | a0001c0001t0003g0044a0001c0001t0011g0003a0001c0001t0011g0091others(19): Show | 23 | HG00544.hp2 HG00741.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-1364_466-1362d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79639477 | |||||
chr5:79639805
|
C | A | 20 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(17): Show | 21 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.466-1046C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639805 | ||||||
chr5:79640068
|
G | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-783G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640068 | ||||||
chr5:79640170
|
C | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-681C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640170 | ||||||
chr5:79640255
|
CA | C | 155 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(152): Show | 158 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.466-580delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79640255 | |||||
chr5:79640274
|
T | C | 1 | a0001c0001t0002g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.466-577T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640274 | ||||||
chr5:79640306
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-545T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640306 | ||||||
chr5:79640373
|
C | T | 1 | a0001c0001t0024g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.466-478C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640373 | ||||||
chr5:79640457
|
C | T | 5 | a0001c0001t0003g0044a0001c0001t0003g0053a0001c0001t0011g0003others(2): Show | 6 | HG00741.hp2 HG01109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-394C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640457 | ||||||
chr5:79640514
|
T | C | 4 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0286others(1): Show | 4 | HG02080.hp2 HG02165.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-337T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640514 | ||||||
chr5:79640694
|
A | C | 1 | a0001c0002t0002g0057 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.466-157A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640694 | ||||||
chr5:79640775
|
AT | A | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-73delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79640775 | |||||
chr5:79640838
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.466-13C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640838 | ||||||
chr5:79641079
|
C | T | 7 | a0001c0001t0001g0248a0001c0001t0001g0301a0001c0001t0001g0310others(4): Show | 7 | HG00609.hp1 NA18941.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-26C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 5/14 | chr5 | 79641079 | ||||||
chr5:79641089
|
T | C | 3 | a0001c0001t0002g0061a0001c0001t0002g0095a0001c0001t0002g0100 | 3 | NA18940.hp1 NA19002.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.581-16T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 5/14 | chr5 | 79641089 | ||||||
chr5:79641437
|
GT | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+254delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 79641437 | |||||
chr5:79641444
|
T | C | 3 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0082 | 3 | HG02559.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.672+248T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641444 | ||||||
chr5:79641498
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+302C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641498 | ||||||
chr5:79641539
|
T | C | 1 | a0001c0001t0046g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.672+343T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641539 | ||||||
chr5:79641686
|
C | G | 1 | a0001c0001t0012g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.672+490C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641686 | ||||||
chr5:79641707
|
TG | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+512delG | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641707 | ||||||
chr5:79641786
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+590G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641786 | ||||||
chr5:79642286
|
T | C | 4 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.673-546T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79642286 | ||||||
chr5:79642379
|
C | T | 1 | a0001c0001t0041g0110 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.673-453C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79642379 | ||||||
chr5:79642492
|
A | G | 218 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(215): Show | 221 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.673-340A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79642492 | ||||||
chr5:79643308
|
T | G | 1 | a0001c0001t0024g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.751+398T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643308 | ||||||
chr5:79643319
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.751+409T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643319 | ||||||
chr5:79643518
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.751+608C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643518 | ||||||
chr5:79643705
|
A | C | 1 | a0001c0001t0003g0006 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.751+795A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643705 | ||||||
chr5:79643724
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.751+814C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643724 | ||||||
chr5:79643728
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.751+818A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643728 | ||||||
chr5:79643956
|
C | G | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.751+1046C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643956 | ||||||
chr5:79643986
|
C | CT | 85 | a0001c0001t0001g0152a0001c0001t0001g0179a0001c0001t0001g0184others(82): Show | 88 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.751+1090dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 79643986 | |||||
chr5:79643986
|
C | CTT | 26 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0079others(23): Show | 26 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.751+1089_751+1090d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 79643986 | |||||
chr5:79644019
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.752-1104A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644019 | ||||||
chr5:79644023
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0018g0137 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.752-1100C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644023 | ||||||
chr5:79644024
|
G | A | 3 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0040g0144 | 3 | HG02486.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.752-1099G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644024 | ||||||
chr5:79644084
|
C | A | 30 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.752-1039C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644084 | ||||||
chr5:79644084
|
C | T | 1 | a0001c0001t0020g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.752-1039C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644084 | ||||||
chr5:79644213
|
C | A | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.752-910C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644213 | ||||||
chr5:79644316
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.752-807G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644316 | ||||||
chr5:79644369
|
T | A | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-754T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644369 | ||||||
chr5:79644469
|
T | G | 1 | a0001c0001t0007g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.752-654T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644469 | ||||||
chr5:79644525
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.752-598T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644525 | ||||||
chr5:79644591
|
C | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.752-532C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644591 | ||||||
chr5:79644837
|
C | T | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-286C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644837 | ||||||
chr5:79644960
|
C | T | 20 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(17): Show | 21 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.752-163C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644960 | ||||||
chr5:79644962
|
A | C | 1 | a0001c0001t0024g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.752-161A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644962 | ||||||
chr5:79645044
|
A | AT | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-73dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 79645044 | |||||
chr5:79645055
|
A | C | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-68A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79645055 | ||||||
chr5:79645526
|
A | T | 1 | a0001c0001t0001g0316 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821+334A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645526 | ||||||
chr5:79645550
|
C | T | 1 | a0001c0001t0005g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.821+358C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645550 | ||||||
chr5:79645745
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.821+553A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645745 | ||||||
chr5:79645839
|
CCACAAAC others(1): Show |
C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.821+652_821+659del others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 79645839 | |||||
chr5:79645858
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.821+666C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645858 | ||||||
chr5:79645930
|
C | G | 1 | a0001c0001t0001g0190 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.821+738C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645930 | ||||||
chr5:79645978
|
C | T | 1 | a0001c0001t0026g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.821+786C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645978 | ||||||
chr5:79646028
|
A | G | 1 | a0001c0001t0006g0208 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.821+836A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646028 | ||||||
chr5:79646180
|
G | A | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.821+988G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646180 | ||||||
chr5:79646336
|
A | G | 1 | a0001c0001t0008g0247 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.821+1144A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646336 | ||||||
chr5:79646442
|
C | T | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.821+1250C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646442 | ||||||
chr5:79646508
|
C | T | 1 | a0001c0001t0012g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.821+1316C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646508 | ||||||
chr5:79646713
|
G | A | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.821+1521G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646713 | ||||||
chr5:79646769
|
CTT | C | 106 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(103): Show | 109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.821+1591_821+1592d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 79646769 | |||||
chr5:79646966
|
G | A | 1 | a0001c0001t0004g0014 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.822-1651G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646966 | ||||||
chr5:79647013
|
T | C | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.822-1604T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647013 | ||||||
chr5:79647269
|
G | T | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.822-1348G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647269 | ||||||
chr5:79647336
|
A | G | 6 | a0001c0001t0002g0034a0001c0001t0002g0061a0001c0001t0002g0090others(3): Show | 6 | HG04228.hp2 NA18940.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.822-1281A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647336 | ||||||
chr5:79647807
|
C | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.822-810C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647807 | ||||||
chr5:79647825
|
G | C | 108 | a0001c0001t0001g0160a0001c0001t0002g0034a0001c0001t0002g0035others(105): Show | 111 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(108): Show |
intron_variant | MODIFIER | c.822-792G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647825 | ||||||
chr5:79648008
|
T | G | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.822-609T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648008 | ||||||
chr5:79648009
|
A | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.822-608A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648009 | ||||||
chr5:79648143
|
T | A | 1 | a0001c0001t0002g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.822-474T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648143 | ||||||
chr5:79648234
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.822-383G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648234 | ||||||
chr5:79648335
|
A | T | 1 | a0001c0001t0017g0142 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.822-282A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648335 | ||||||
chr5:79648356
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.822-261G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648356 | ||||||
chr5:79648472
|
G | A | 2 | a0001c0001t0003g0079a0001c0001t0011g0007 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.822-145G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648472 | ||||||
chr5:79648499
|
C | G | 1 | a0001c0001t0040g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.822-118C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648499 | ||||||
chr5:79648548
|
G | C | 30 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.822-69G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648548 | ||||||
chr5:79648582
|
A | G | 1 | a0001c0001t0006g0208 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.822-35A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648582 | ||||||
chr5:79648611
|
A | T | 1 | a0001c0001t0024g0023 | 1 | HG02965.hp2 | splice_region_variant&intron_variant | LOW | c.822-6A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648611 | ||||||
chr5:79648961
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.899-101G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 9/14 | chr5 | 79648961 | ||||||
chr5:79649266
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1027+76A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649266 | ||||||
chr5:79649348
|
C | T | 148 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(145): Show | 151 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1027+158C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649348 | ||||||
chr5:79649386
|
G | GT | 96 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(93): Show | 99 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1027+207dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79649386 | |||||
chr5:79649386
|
G | GTT | 6 | a0001c0001t0003g0008a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027+206_1027+207d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79649386 | |||||
chr5:79649398
|
A | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+208A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649398 | ||||||
chr5:79649505
|
G | T | 1 | a0001c0002t0002g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1027+315G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649505 | ||||||
chr5:79649888
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+698G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649888 | ||||||
chr5:79649913
|
T | C | 164 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(161): Show | 167 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.1027+723T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649913 | ||||||
chr5:79650012
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+822A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650012 | ||||||
chr5:79650046
|
A | C | 72 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(69): Show | 74 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1027+856A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650046 | ||||||
chr5:79650149
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1027+959A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650149 | ||||||
chr5:79650182
|
A | G | 1 | a0001c0001t0005g0127 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1027+992A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650182 | ||||||
chr5:79650223
|
A | G | 2 | a0001c0001t0004g0086a0001c0001t0011g0026 | 2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1027+1033A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650223 | ||||||
chr5:79650243
|
T | C | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1027+1053T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650243 | ||||||
chr5:79650392
|
C | G | 41 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(38): Show | 41 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1027+1202C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650392 | ||||||
chr5:79650530
|
C | T | 1 | a0001c0001t0013g0224 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1027+1340C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650530 | ||||||
chr5:79650699
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+1509C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650699 | ||||||
chr5:79650939
|
G | C | 1 | a0001c0001t0001g0151 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1027+1749G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650939 | ||||||
chr5:79650979
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1027+1789A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650979 | ||||||
chr5:79651031
|
C | T | 1 | a0001c0001t0020g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1027+1841C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651031 | ||||||
chr5:79651032
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1027+1842A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651032 | ||||||
chr5:79651220
|
A | T | 5 | a0001c0001t0006g0004a0001c0001t0006g0289a0001c0001t0006g0322others(2): Show | 6 | HG01358.hp2 HG01943.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027+2030A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651220 | ||||||
chr5:79651227
|
G | A | 1 | a0001c0001t0005g0114 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1027+2037G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651227 | ||||||
chr5:79651395
|
C | CA | 10 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0086others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1027+2215dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79651395 | |||||
chr5:79651464
|
CA | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+2276delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79651464 | |||||
chr5:79651835
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0287others(2): Show | 5 | HG01516.hp2 HG01517.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+2645T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651835 | ||||||
chr5:79651840
|
G | A | 60 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(57): Show | 62 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1027+2650G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651840 | ||||||
chr5:79651906
|
A | G | 14 | a0001c0001t0004g0010a0001c0001t0004g0014a0001c0001t0004g0015others(11): Show | 14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1027+2716A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651906 | ||||||
chr5:79652010
|
A | T | 1 | a0001c0001t0018g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1027+2820A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652010 | ||||||
chr5:79652024
|
A | G | 2 | a0001c0001t0004g0014a0001c0001t0004g0081 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1027+2834A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652024 | ||||||
chr5:79652131
|
C | T | 1 | a0001c0002t0023g0106 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1027+2941C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652131 | ||||||
chr5:79652353
|
C | T | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1027+3163C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652353 | ||||||
chr5:79652572
|
CA | C | 19 | a0001c0001t0001g0145a0001c0001t0001g0248a0001c0001t0001g0301others(16): Show | 19 | HG00423.hp1 HG00609.hp1 NA18941.hp1 others(16): Show |
intron_variant | MODIFIER | c.1027+3386delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79652572 | |||||
chr5:79652723
|
G | A | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1027+3533G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652723 | ||||||
chr5:79652805
|
A | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0287a0001c0001t0001g0329 | 3 | HG01516.hp2 HG01517.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1027+3615A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652805 | ||||||
chr5:79652844
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+3654A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652844 | ||||||
chr5:79652882
|
T | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+3692T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652882 | ||||||
chr5:79653097
|
G | C | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1028-3861G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653097 | ||||||
chr5:79653148
|
A | T | 154 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(151): Show | 157 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1028-3810A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653148 | ||||||
chr5:79653514
|
T | A | 1 | a0001c0001t0001g0313 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1028-3444T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653514 | ||||||
chr5:79653590
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-3368A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653590 | ||||||
chr5:79653641
|
C | T | 1 | a0001c0001t0007g0198 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1028-3317C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653641 | ||||||
chr5:79654054
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-2904A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654054 | ||||||
chr5:79654085
|
C | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-2873C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654085 | ||||||
chr5:79654128
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-2830T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654128 | ||||||
chr5:79654159
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1028-2799C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654159 | ||||||
chr5:79654212
|
A | G | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1028-2746A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654212 | ||||||
chr5:79654235
|
T | C | 219 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(216): Show | 222 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.1028-2723T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654235 | ||||||
chr5:79654286
|
C | A | 1 | a0001c0001t0001g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1028-2672C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654286 | ||||||
chr5:79654528
|
A | G | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0214others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-2430A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654528 | ||||||
chr5:79654548
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-2410T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654548 | ||||||
chr5:79654580
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1028-2378G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654580 | ||||||
chr5:79654584
|
C | T | 108 | a0001c0001t0001g0220a0001c0001t0002g0034a0001c0001t0002g0035others(105): Show | 111 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(108): Show |
intron_variant | MODIFIER | c.1028-2374C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654584 | ||||||
chr5:79654677
|
T | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0167 | 2 | HG01255.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1028-2281T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654677 | ||||||
chr5:79654763
|
C | CA | 13 | a0001c0001t0002g0076a0001c0001t0003g0070a0001c0001t0004g0071others(10): Show | 13 | HG01167.hp2 HG02486.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1028-2184dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79654763 | |||||
chr5:79654763
|
CA | C | 36 | a0001c0001t0001g0161a0001c0001t0003g0006a0001c0001t0003g0008others(33): Show | 37 | HG01256.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.1028-2184delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79654763 | |||||
chr5:79654806
|
G | A | 3 | a0001c0001t0002g0060a0001c0001t0003g0055a0001c0001t0046g0064 | 3 | NA18947.hp1 NA18973.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1028-2152G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654806 | ||||||
chr5:79654807
|
C | T | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1028-2151C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654807 | ||||||
chr5:79654983
|
C | G | 2 | a0001c0001t0001g0138a0001c0001t0018g0137 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1028-1975C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654983 | ||||||
chr5:79655072
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-1886G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655072 | ||||||
chr5:79655253
|
A | G | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1028-1705A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655253 | ||||||
chr5:79655456
|
G | A | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1028-1502G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655456 | ||||||
chr5:79655536
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1028-1422T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655536 | ||||||
chr5:79655566
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1028-1392A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655566 | ||||||
chr5:79655651
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-1307G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655651 | ||||||
chr5:79655667
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-1291G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655667 | ||||||
chr5:79655744
|
G | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-1214G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655744 | ||||||
chr5:79655746
|
GT | G | 104 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(101): Show | 107 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.1028-1198delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79655746 | |||||
chr5:79655891
|
C | T | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1028-1067C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655891 | ||||||
chr5:79655895
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1028-1063G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655895 | ||||||
chr5:79656041
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-917A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656041 | ||||||
chr5:79656117
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1028-841A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656117 | ||||||
chr5:79656241
|
A | ATTAAT | 211 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(208): Show | 214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1028-716_1028-712d others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79656241 | |||||
chr5:79656329
|
T | G | 11 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0168others(8): Show | 11 | HG00639.hp1 HG01175.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1028-629T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656329 | ||||||
chr5:79656467
|
T | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-491T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656467 | ||||||
chr5:79656841
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1028-117T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656841 | ||||||
chr5:79656843
|
G | T | 1 | a0001c0001t0001g0233 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1028-115G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656843 | ||||||
chr5:79656844
|
T | G | 1 | a0001c0001t0001g0233 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1028-114T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656844 | ||||||
chr5:79656868
|
G | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-90G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656868 | ||||||
chr5:79656871
|
C | T | 3 | a0001c0001t0003g0008a0001c0001t0003g0079a0001c0001t0011g0007 | 3 | HG03139.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1028-87C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656871 | ||||||
chr5:79657120
|
A | G | 1 | a0001c0001t0012g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1071+119A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657120 | ||||||
chr5:79657197
|
A | C | 1 | a0001c0001t0001g0233 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1071+196A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657197 | ||||||
chr5:79657460
|
AATACACC others(6625): Show |
A | 5 | a0001c0001t0001g0235a0001c0001t0001g0240a0001c0001t0001g0252others(2): Show | 5 | HG00544.hp1 HG02015.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+463_1072-4797 others(3): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79657460 | |||||
chr5:79657651
|
T | G | 1 | a0001c0001t0007g0198 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1071+650T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657651 | ||||||
chr5:79657789
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1071+788A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657789 | ||||||
chr5:79657962
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+961A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657962 | ||||||
chr5:79658014
|
G | T | 59 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(56): Show | 61 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1071+1013G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658014 | ||||||
chr5:79658267
|
T | G | 72 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(69): Show | 74 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1071+1266T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658267 | ||||||
chr5:79658298
|
A | T | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+1297A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658298 | ||||||
chr5:79658358
|
CT | C | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1071+1371delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79658358 | |||||
chr5:79658429
|
G | A | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+1428G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658429 | ||||||
chr5:79658503
|
T | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+1502T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658503 | ||||||
chr5:79658677
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1071+1676T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658677 | ||||||
chr5:79658758
|
C | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+1757C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658758 | ||||||
chr5:79658837
|
A | C | 3 | a0001c0001t0004g0072a0001c0001t0004g0073a0001c0001t0027g0075 | 3 | HG02809.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1071+1836A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658837 | ||||||
chr5:79658860
|
T | TTATC | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+1861_1071+186 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79658860 | |||||
chr5:79659016
|
G | T | 30 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1071+2015G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659016 | ||||||
chr5:79659172
|
G | A | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+2171G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659172 | ||||||
chr5:79659494
|
T | G | 20 | a0001c0001t0001g0145a0001c0001t0001g0248a0001c0001t0001g0301others(17): Show | 20 | HG00423.hp1 HG00609.hp1 NA18941.hp1 others(17): Show |
intron_variant | MODIFIER | c.1071+2493T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659494 | ||||||
chr5:79659496
|
T | C | 20 | a0001c0001t0001g0145a0001c0001t0001g0248a0001c0001t0001g0301others(17): Show | 20 | HG00423.hp1 HG00609.hp1 NA18941.hp1 others(17): Show |
intron_variant | MODIFIER | c.1071+2495T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659496 | ||||||
chr5:79659507
|
C | T | 1 | a0001c0001t0005g0126 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1071+2506C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659507 | ||||||
chr5:79659531
|
C | CA | 10 | a0001c0001t0001g0155a0001c0001t0001g0231a0001c0001t0001g0273others(7): Show | 10 | HG02647.hp1 HG02970.hp2 HG04228.hp1 others(7): Show |
intron_variant | MODIFIER | c.1071+2553dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659531 | |||||
chr5:79659552
|
AAATGTAT others(4): Show |
A | 1 | a0001c0001t0001g0295 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1071+2553_1071+256 others(15): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659552 | |||||
chr5:79659553
|
A | AAAATGTA others(3): Show |
1 | a0001c0001t0001g0280 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGT | 9 | a0001c0001t0001g0270a0001c0001t0001g0276a0001c0001t0001g0286others(6): Show | 9 | HG00423.hp1 HG01175.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(9): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT | 15 | a0001c0001t0001g0158a0001c0001t0001g0225a0001c0001t0001g0266others(12): Show | 15 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(11): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT others(2): Show |
6 | a0001c0001t0001g0211a0001c0001t0001g0230a0001c0001t0001g0325others(3): Show | 6 | HG02004.hp2 HG02922.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(13): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT others(4): Show |
4 | a0001c0001t0001g0190a0001c0001t0001g0312a0001c0001t0001g0323others(1): Show | 4 | HG00673.hp1 HG01257.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(15): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT others(6): Show |
2 | a0001c0001t0001g0145a0001c0001t0001g0160 | 2 | HG01934.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(17): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT others(8): Show |
3 | a0001c0001t0001g0238a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG03490.hp1 HG03492.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(19): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT others(10): Show |
1 | a0001c0001t0001g0239 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(21): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT others(12): Show |
2 | a0001c0001t0001g0203a0001c0001t0001g0265 | 2 | NA18964.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(23): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT others(14): Show |
1 | a0001c0001t0001g0281 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(25): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT others(16): Show |
1 | a0001c0001t0001g0278 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(27): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | AAATGTAT others(24): Show |
1 | a0001c0001t0001g0292 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(35): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
A | ATGTAT | 3 | a0001c0001t0001g0192a0001c0001t0001g0219a0001c0001t0013g0245 | 3 | HG02258.hp2 HG02683.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1071+2552_1071+255 others(9): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659553 | ||||||
chr5:79659553
|
A | ATGTATAT | 4 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0216others(1): Show | 4 | HG01884.hp2 HG02004.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+2552_1071+255 others(11): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659553 | ||||||
chr5:79659553
|
A | ATGTATAT others(4): Show |
1 | a0001c0001t0001g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1071+2552_1071+255 others(15): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659553 | ||||||
chr5:79659553
|
A | ATGTATAT others(10): Show |
1 | a0001c0001t0001g0220 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1071+2552_1071+255 others(21): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659553 | ||||||
chr5:79659553
|
AATGTAT | A | 7 | a0001c0001t0002g0042a0001c0001t0003g0011a0001c0001t0009g0027others(4): Show | 7 | HG01167.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071+2555_1071+256 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
AATGTATA others(1): Show |
A | 52 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(49): Show | 53 | HG00673.hp2 HG01109.hp1 HG01433.hp2 others(50): Show |
intron_variant | MODIFIER | c.1071+2555_1071+256 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659553
|
AATGTATA others(9): Show |
A | 3 | a0001c0001t0003g0096a0001c0003t0010g0037a0001c0003t0010g0093 | 3 | NA18962.hp2 NA19010.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1071+2555_1071+257 others(20): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | |||||
chr5:79659554
|
A | AATG | 25 | a0001c0001t0001g0207a0001c0001t0001g0221a0001c0001t0001g0248others(22): Show | 26 | HG00408.hp1 HG01358.hp2 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | ||||||
chr5:79659554
|
AT | A | 5 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0009g0104others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+2554delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | ||||||
chr5:79659554
|
ATGT | A | 7 | a0001c0001t0001g0209a0001c0001t0004g0071a0001c0001t0005g0122others(4): Show | 7 | HG01243.hp2 HG02615.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1071+2554_1071+255 others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | ||||||
chr5:79659554
|
ATGTAT | A | 4 | a0001c0001t0004g0072a0001c0001t0004g0073a0001c0001t0020g0133others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+2554_1071+255 others(9): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | ||||||
chr5:79659554
|
ATGTATAT | A | 19 | a0001c0001t0002g0063a0001c0001t0003g0006a0001c0001t0003g0009others(16): Show | 20 | HG00544.hp2 HG00741.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.1071+2554_1071+256 others(11): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | ||||||
chr5:79659554
|
ATGTATAT others(2): Show |
A | 16 | a0001c0001t0002g0068a0001c0001t0004g0010a0001c0001t0004g0014others(13): Show | 17 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1071+2554_1071+256 others(13): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | ||||||
chr5:79659554
|
ATGTATAT others(6): Show |
A | 1 | a0001c0001t0001g0222 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1071+2554_1071+256 others(17): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | ||||||
chr5:79659554
|
ATGTATAT others(8): Show |
A | 1 | a0001c0003t0010g0094 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1071+2554_1071+256 others(19): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | ||||||
chr5:79659554
|
ATGTATAT others(10): Show |
A | 1 | a0001c0001t0035g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1071+2554_1071+257 others(21): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | ||||||
chr5:79659556
|
G | A | 92 | a0001c0001t0001g0145a0001c0001t0001g0158a0001c0001t0001g0160others(89): Show | 93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1071+2555G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659556 | ||||||
chr5:79659556
|
G | GTA | 15 | a0001c0001t0001g0139a0001c0001t0001g0229a0001c0001t0001g0236others(12): Show | 15 | HG00140.hp1 HG01109.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1071+2592_1071+259 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
G | GTATA | 13 | a0001c0001t0001g0164a0001c0001t0001g0172a0001c0001t0001g0179others(10): Show | 13 | HG00140.hp2 HG00639.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1071+2590_1071+259 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
G | GTATATA | 17 | a0001c0001t0001g0135a0001c0001t0001g0159a0001c0001t0001g0162others(14): Show | 17 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1071+2588_1071+259 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0141a0001c0001t0001g0152a0001c0001t0001g0166others(4): Show | 7 | HG01243.hp1 HG01975.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071+2586_1071+259 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
G | GTATATAT others(3): Show |
4 | a0001c0001t0001g0161a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG01175.hp2 HG01256.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+2584_1071+259 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
G | GTATATAT others(5): Show |
5 | a0001c0001t0001g0177a0001c0001t0001g0212a0001c0001t0008g0210others(2): Show | 5 | HG01074.hp1 HG01255.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+2582_1071+259 others(16): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
G | GTGTATAT others(3): Show |
1 | a0001c0001t0001g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1071+2556_1071+255 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
GTA | G | 13 | a0001c0001t0001g0138a0001c0001t0001g0151a0001c0001t0001g0156others(10): Show | 13 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.1071+2592_1071+259 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
GTATA | G | 15 | a0001c0001t0001g0251a0001c0001t0001g0304a0001c0001t0005g0114others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1071+2590_1071+259 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
GTATATA | G | 7 | a0001c0001t0001g0140a0001c0001t0005g0116a0001c0001t0005g0117others(4): Show | 7 | HG02602.hp1 HG02602.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071+2588_1071+259 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
GTATATAT others(3): Show |
G | 1 | a0001c0001t0005g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1071+2584_1071+259 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659556
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1071+2578_1071+259 others(20): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | |||||
chr5:79659557
|
T | A | 4 | a0001c0001t0003g0070a0001c0001t0009g0104a0001c0001t0026g0069others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+2556T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659557 | ||||||
chr5:79659558
|
A | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+2557A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659558 | ||||||
chr5:79659559
|
T | A | 9 | a0001c0001t0002g0076a0001c0001t0003g0070a0001c0001t0004g0071others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+2558T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659559 | ||||||
chr5:79659560
|
A | G | 9 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0005g0122others(6): Show | 9 | HG01243.hp2 HG02080.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1071+2559A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659560 | ||||||
chr5:79659561
|
T | A | 13 | a0001c0001t0002g0042a0001c0001t0002g0076a0001c0001t0003g0011others(10): Show | 13 | HG01167.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1071+2560T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659561 | ||||||
chr5:79659562
|
A | G | 9 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0003g0070others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+2561A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659562 | ||||||
chr5:79659563
|
T | A | 74 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(71): Show | 76 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.1071+2562T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659563 | ||||||
chr5:79659564
|
A | G | 11 | a0001c0001t0002g0042a0001c0001t0002g0076a0001c0001t0004g0072others(8): Show | 11 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1071+2563A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659564 | ||||||
chr5:79659565
|
T | A | 32 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(29): Show | 33 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1071+2564T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659565 | ||||||
chr5:79659566
|
A | G | 62 | a0001c0001t0001g0295a0001c0001t0002g0034a0001c0001t0002g0035others(59): Show | 64 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1071+2565A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659566 | ||||||
chr5:79659568
|
A | G | 31 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(28): Show | 32 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(29): Show |
intron_variant | MODIFIER | c.1071+2567A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659568 | ||||||
chr5:79659570
|
A | G | 7 | a0001c0001t0001g0222a0001c0001t0003g0070a0001c0001t0004g0071others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071+2569A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659570 | ||||||
chr5:79659571
|
T | A | 4 | a0001c0001t0003g0096a0001c0003t0010g0037a0001c0003t0010g0093others(1): Show | 4 | NA18962.hp2 NA19000.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+2570T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659571 | ||||||
chr5:79659572
|
A | G | 8 | a0001c0001t0002g0042a0001c0001t0002g0076a0001c0001t0004g0072others(5): Show | 8 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1071+2571A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659572 | ||||||
chr5:79659574
|
A | G | 63 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(60): Show | 65 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1071+2573A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659574 | ||||||
chr5:79659576
|
A | G | 31 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(28): Show | 32 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(29): Show |
intron_variant | MODIFIER | c.1071+2575A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659576 | ||||||
chr5:79659595
|
A | G | 1 | a0001c0001t0006g0333 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1071+2594A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659595 | ||||||
chr5:79659597
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1071+2596A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659597 | ||||||
chr5:79659604
|
G | A | 1 | a0001c0001t0012g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1071+2603G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659604 | ||||||
chr5:79659687
|
G | A | 1 | a0001c0001t0030g0186 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1071+2686G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659687 | ||||||
chr5:79659735
|
A | G | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+2734A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659735 | ||||||
chr5:79659739
|
T | G | 1 | a0001c0001t0006g0330 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1071+2738T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659739 | ||||||
chr5:79659880
|
A | AT | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+2880dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659880 | |||||
chr5:79659954
|
G | A | 216 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(213): Show | 219 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1071+2953G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659954 | ||||||
chr5:79659987
|
C | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071+2986C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659987 | ||||||
chr5:79659993
|
G | T | 1 | a0001c0002t0016g0108 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1071+2992G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659993 | ||||||
chr5:79660016
|
C | G | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071+3015C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660016 | ||||||
chr5:79660216
|
CTG | C | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+3217_1071+321 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79660216 | |||||
chr5:79660249
|
A | G | 30 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1071+3248A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660249 | ||||||
chr5:79660268
|
G | C | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+3267G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660268 | ||||||
chr5:79660369
|
A | G | 1 | a0001c0007t0025g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1071+3368A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660369 | ||||||
chr5:79660482
|
CATTT | C | 30 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1071+3484_1071+348 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79660482 | |||||
chr5:79660588
|
A | G | 1 | a0001c0001t0005g0122 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1071+3587A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660588 | ||||||
chr5:79660650
|
C | T | 3 | a0001c0001t0004g0072a0001c0001t0004g0073a0001c0001t0027g0075 | 3 | HG02809.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1071+3649C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660650 | ||||||
chr5:79660796
|
G | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+3795G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660796 | ||||||
chr5:79661005
|
A | G | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071+4004A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661005 | ||||||
chr5:79661009
|
A | T | 3 | a0001c0001t0004g0071a0001c0001t0009g0077a0001c0001t0009g0104 | 3 | HG02615.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1071+4008A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661009 | ||||||
chr5:79661055
|
T | C | 4 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+4054T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661055 | ||||||
chr5:79661088
|
G | A | 1 | a0001c0001t0045g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1071+4087G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661088 | ||||||
chr5:79661720
|
G | A | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+4719G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661720 | ||||||
chr5:79662021
|
A | G | 1 | a0001c0001t0024g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1071+5020A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662021 | ||||||
chr5:79662163
|
G | A | 30 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1071+5162G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662163 | ||||||
chr5:79662165
|
T | G | 5 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0042others(2): Show | 5 | HG00673.hp2 HG02083.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+5164T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662165 | ||||||
chr5:79662168
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1071+5167A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662168 | ||||||
chr5:79662396
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1071+5395C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662396 | ||||||
chr5:79662543
|
G | A | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+5542G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662543 | ||||||
chr5:79662667
|
G | A | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+5666G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662667 | ||||||
chr5:79662726
|
G | A | 4 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(1): Show | 4 | HG03654.hp2 HG03927.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+5725G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662726 | ||||||
chr5:79662905
|
C | T | 2 | a0001c0001t0003g0009a0001c0001t0003g0011 | 2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1071+5904C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662905 | ||||||
chr5:79663230
|
G | C | 2 | a0001c0001t0042g0339a0001c0001t0045g0005 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1072-5662G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663230 | ||||||
chr5:79663256
|
G | A | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072-5636G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663256 | ||||||
chr5:79663279
|
A | T | 1 | a0001c0001t0030g0186 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1072-5613A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663279 | ||||||
chr5:79663282
|
C | A | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-5610C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663282 | ||||||
chr5:79663296
|
G | C | 14 | a0001c0001t0004g0010a0001c0001t0004g0014a0001c0001t0004g0015others(11): Show | 14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1072-5596G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663296 | ||||||
chr5:79663307
|
A | G | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-5585A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663307 | ||||||
chr5:79663335
|
G | A | 2 | a0001c0001t0020g0130a0001c0001t0020g0133 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1072-5557G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663335 | ||||||
chr5:79663559
|
T | C | 209 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(206): Show | 212 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1072-5333T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663559 | ||||||
chr5:79663820
|
C | T | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-5072C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663820 | ||||||
chr5:79663894
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0017g0136 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1072-4998C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663894 | ||||||
chr5:79663917
|
G | A | 209 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(206): Show | 212 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1072-4975G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663917 | ||||||
chr5:79663923
|
G | C | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-4969G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663923 | ||||||
chr5:79663931
|
T | C | 2 | a0001c0001t0038g0226a0001c0001t0041g0110 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1072-4961T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663931 | ||||||
chr5:79664207
|
A | G | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072-4685A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664207 | ||||||
chr5:79664392
|
C | T | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-4500C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664392 | ||||||
chr5:79664488
|
C | T | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1072-4404C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664488 | ||||||
chr5:79664551
|
C | T | 12 | a0001c0001t0001g0207a0001c0001t0001g0222a0001c0001t0001g0264others(9): Show | 12 | HG00408.hp1 NA18940.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-4341C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664551 | ||||||
chr5:79664594
|
C | CA | 31 | a0001c0001t0001g0335a0001c0001t0005g0111a0001c0001t0005g0114others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1072-4282dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79664594 | |||||
chr5:79664594
|
CA | C | 105 | a0001c0001t0001g0206a0001c0001t0002g0034a0001c0001t0002g0035others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-4282delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79664594 | |||||
chr5:79664919
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1072-3973C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664919 | ||||||
chr5:79665129
|
A | G | 1 | a0001c0001t0022g0078 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1072-3763A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665129 | ||||||
chr5:79665270
|
G | A | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1072-3622G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665270 | ||||||
chr5:79665451
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0259 | 2 | NA19078.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1072-3441T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665451 | ||||||
chr5:79665790
|
G | A | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1072-3102G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665790 | ||||||
chr5:79665849
|
G | T | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-3043G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665849 | ||||||
chr5:79665896
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1072-2996C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665896 | ||||||
chr5:79665941
|
T | G | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1072-2951T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665941 | ||||||
chr5:79666050
|
G | T | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1072-2842G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666050 | ||||||
chr5:79666069
|
A | G | 31 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1072-2823A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666069 | ||||||
chr5:79666091
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0018g0137 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1072-2801C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666091 | ||||||
chr5:79666188
|
C | T | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-2704C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666188 | ||||||
chr5:79666208
|
C | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1072-2684C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666208 | ||||||
chr5:79666240
|
C | T | 4 | a0001c0001t0004g0071a0001c0001t0009g0077a0001c0001t0009g0104others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1072-2652C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666240 | ||||||
chr5:79666242
|
G | T | 1 | a0001c0001t0003g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1072-2650G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666242 | ||||||
chr5:79666245
|
T | TC | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-2645dupC | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79666245 | |||||
chr5:79666331
|
C | G | 8 | a0001c0001t0005g0120a0001c0001t0005g0122a0001c0001t0005g0123others(5): Show | 8 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1072-2561C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666331 | ||||||
chr5:79666351
|
A | C | 1 | a0001c0001t0001g0337 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1072-2541A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666351 | ||||||
chr5:79666484
|
A | G | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-2408A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666484 | ||||||
chr5:79666495
|
TCATCACC others(37): Show |
T | 5 | a0001c0001t0002g0036a0001c0001t0002g0046a0001c0001t0002g0063others(2): Show | 5 | HG02155.hp2 NA18945.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1072-2352_1072-230 others(48): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79666495 | |||||
chr5:79666611
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1072-2281C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666611 | ||||||
chr5:79666655
|
A | ATTATAC | 217 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(214): Show | 220 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1072-2234_1072-223 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79666655 | |||||
chr5:79666769
|
A | G | 1 | a0001c0001t0007g0128 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1072-2123A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666769 | ||||||
chr5:79666984
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1072-1908A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666984 | ||||||
chr5:79667156
|
G | C | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-1736G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667156 | ||||||
chr5:79667168
|
A | G | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-1724A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667168 | ||||||
chr5:79667233
|
T | C | 14 | a0001c0001t0004g0010a0001c0001t0004g0014a0001c0001t0004g0015others(11): Show | 14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1072-1659T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667233 | ||||||
chr5:79667290
|
G | A | 104 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(101): Show | 107 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.1072-1602G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667290 | ||||||
chr5:79667292
|
G | C | 34 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(31): Show | 35 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.1072-1600G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667292 | ||||||
chr5:79667390
|
A | G | 163 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(160): Show | 166 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.1072-1502A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667390 | ||||||
chr5:79667500
|
C | A | 30 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1072-1392C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667500 | ||||||
chr5:79667528
|
T | C | 1 | a0001c0001t0003g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1072-1364T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667528 | ||||||
chr5:79667882
|
G | GT | 210 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(207): Show | 213 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.1072-1010_1072-100 others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667882 | ||||||
chr5:79667899
|
C | T | 9 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0001g0240others(6): Show | 9 | HG00544.hp1 HG02015.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.1072-993C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667899 | ||||||
chr5:79667931
|
CT | C | 8 | a0001c0001t0002g0060a0001c0001t0019g0131a0001c0001t0019g0132others(5): Show | 8 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1072-947delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79667931 | |||||
chr5:79667957
|
A | C | 105 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(102): Show | 108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-935A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667957 | ||||||
chr5:79668176
|
G | A | 210 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(207): Show | 213 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.1072-716G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79668176 | ||||||
chr5:79668766
|
C | CCAAATTG others(20): Show |
3 | a0001c0001t0006g0275a0001c0001t0008g0263a0001c0001t0008g0267 | 3 | NA18965.hp2 NA18979.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1072-124_1072-98du others(28): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79668766 | |||||
chr5:79669064
|
A | ATG | 46 | a0001c0001t0001g0206a0001c0001t0004g0071a0001c0001t0005g0111others(43): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208+50_1208+51dup others(2): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79669064 | |||||
chr5:79669239
|
T | G | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1208+211T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669239 | ||||||
chr5:79669425
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1208+397G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669425 | ||||||
chr5:79669520
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0175 | 2 | HG00597.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1208+492A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669520 | ||||||
chr5:79669640
|
G | T | 1 | a0001c0001t0006g0333 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1208+612G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669640 | ||||||
chr5:79669770
|
A | G | 2 | a0001c0001t0005g0114a0001c0001t0005g0146 | 2 | HG03831.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1208+742A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669770 | ||||||
chr5:79669869
|
C | G | 7 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208+841C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669869 | ||||||
chr5:79670061
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1208+1033A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670061 | ||||||
chr5:79670189
|
A | G | 5 | a0001c0001t0003g0096a0001c0003t0010g0037a0001c0003t0010g0089others(2): Show | 5 | NA18947.hp2 NA18962.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+1161A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670189 | ||||||
chr5:79670226
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1208+1198A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670226 | ||||||
chr5:79670236
|
A | G | 19 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0001g0238others(16): Show | 20 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1208+1208A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670236 | ||||||
chr5:79670285
|
C | T | 11 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0168others(8): Show | 11 | HG00639.hp1 HG01175.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1208+1257C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670285 | ||||||
chr5:79670311
|
T | TTTTA | 5 | a0001c0001t0014g0119a0001c0001t0019g0131a0001c0001t0019g0132others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+1307_1208+131 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79670311 | |||||
chr5:79670394
|
G | A | 1 | a0001c0001t0006g0289 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1208+1366G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670394 | ||||||
chr5:79670481
|
C | T | 1 | a0001c0001t0007g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1208+1453C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670481 | ||||||
chr5:79670613
|
G | A | 1 | a0001c0001t0038g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1208+1585G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670613 | ||||||
chr5:79670618
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1208+1590C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670618 | ||||||
chr5:79670673
|
A | G | 1 | a0001c0002t0012g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1208+1645A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670673 | ||||||
chr5:79670695
|
G | A | 4 | a0001c0001t0001g0233a0001c0001t0001g0256a0001c0001t0001g0259others(1): Show | 4 | HG02040.hp1 HG02132.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208+1667G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670695 | ||||||
chr5:79670733
|
T | C | 1 | a0002c0004t0003g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1208+1705T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670733 | ||||||
chr5:79670867
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1208+1839C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670867 | ||||||
chr5:79670992
|
G | C | 1 | a0001c0001t0018g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1208+1964G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670992 | ||||||
chr5:79671049
|
T | C | 1 | a0001c0001t0026g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1208+2021T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671049 | ||||||
chr5:79671120
|
G | T | 4 | a0001c0002t0002g0049a0001c0002t0002g0051a0001c0002t0002g0056others(1): Show | 4 | HG01433.hp2 HG01934.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208+2092G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671120 | ||||||
chr5:79671222
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1208+2194A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671222 | ||||||
chr5:79671249
|
G | C | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208+2221G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671249 | ||||||
chr5:79671700
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0216 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1208+2672C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671700 | ||||||
chr5:79672011
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0287 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1208+2983A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672011 | ||||||
chr5:79672084
|
T | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208+3056T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672084 | ||||||
chr5:79672102
|
C | CA | 169 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(166): Show | 171 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(168): Show |
intron_variant | MODIFIER | c.1208+3085dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79672102 | |||||
chr5:79672118
|
A | C | 1 | a0001c0001t0004g0001 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1208+3090A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672118 | ||||||
chr5:79672549
|
C | A | 35 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(32): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.1208+3521C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672549 | ||||||
chr5:79672607
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1208+3579A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672607 | ||||||
chr5:79672642
|
T | G | 2 | a0001c0001t0019g0131a0001c0001t0019g0132 | 2 | HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1208+3614T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672642 | ||||||
chr5:79672652
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1208+3624T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672652 | ||||||
chr5:79672667
|
C | G | 59 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(56): Show | 61 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1208+3639C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672667 | ||||||
chr5:79672784
|
T | C | 31 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1208+3756T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672784 | ||||||
chr5:79672837
|
C | G | 2 | a0001c0001t0001g0233a0001c0001t0001g0259 | 2 | NA19078.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1208+3809C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672837 | ||||||
chr5:79672945
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1208+3917G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672945 | ||||||
chr5:79672986
|
T | G | 1 | a0001c0001t0035g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1208+3958T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672986 | ||||||
chr5:79673167
|
T | A | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1208+4139T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673167 | ||||||
chr5:79673391
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1208+4363T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673391 | ||||||
chr5:79673449
|
A | G | 314 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1208+4421A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673449 | ||||||
chr5:79673534
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1208+4506A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673534 | ||||||
chr5:79673564
|
G | A | 35 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(32): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.1208+4536G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673564 | ||||||
chr5:79673568
|
G | GT | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1208+4541dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79673568 | |||||
chr5:79673846
|
C | T | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1208+4818C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673846 | ||||||
chr5:79674018
|
G | C | 12 | a0001c0001t0002g0076a0001c0001t0003g0070a0001c0001t0004g0071others(9): Show | 12 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1208+4990G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674018 | ||||||
chr5:79674144
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1208+5116G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674144 | ||||||
chr5:79674158
|
C | T | 5 | a0001c0001t0001g0235a0001c0001t0001g0240a0001c0001t0001g0252others(2): Show | 5 | HG00544.hp1 HG02015.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208+5130C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674158 | ||||||
chr5:79674267
|
A | G | 3 | a0001c0001t0002g0061a0001c0001t0002g0095a0001c0001t0002g0100 | 3 | NA18940.hp1 NA19002.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1208+5239A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674267 | ||||||
chr5:79674312
|
T | G | 206 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(203): Show | 209 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1209-5267T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674312 | ||||||
chr5:79674380
|
C | T | 1 | a0001c0001t0006g0291 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1209-5199C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674380 | ||||||
chr5:79674483
|
A | C | 4 | a0001c0001t0001g0233a0001c0001t0001g0256a0001c0001t0001g0259others(1): Show | 4 | HG02040.hp1 HG02132.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209-5096A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674483 | ||||||
chr5:79674535
|
A | G | 3 | a0001c0001t0001g0244a0001c0001t0008g0319a0001c0001t0013g0224 | 3 | HG01255.hp2 HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1209-5044A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674535 | ||||||
chr5:79674655
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1209-4924A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674655 | ||||||
chr5:79674780
|
A | G | 108 | a0001c0001t0001g0175a0001c0001t0002g0034a0001c0001t0002g0035others(105): Show | 111 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(108): Show |
intron_variant | MODIFIER | c.1209-4799A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674780 | ||||||
chr5:79674966
|
C | G | 2 | a0001c0001t0014g0118a0001c0001t0014g0119 | 2 | HG00099.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1209-4613C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674966 | ||||||
chr5:79675106
|
A | T | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1209-4473A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79675106 | ||||||
chr5:79675265
|
G | A | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-4314G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79675265 | ||||||
chr5:79675337
|
G | A | 5 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0251others(2): Show | 5 | HG00597.hp1 HG00673.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.1209-4242G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79675337 | ||||||
chr5:79675984
|
C | G | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-3595C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79675984 | ||||||
chr5:79676111
|
T | G | 14 | a0001c0001t0004g0010a0001c0001t0004g0014a0001c0001t0004g0015others(11): Show | 14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1209-3468T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676111 | ||||||
chr5:79676152
|
A | C | 1 | a0001c0001t0006g0340 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1209-3427A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676152 | ||||||
chr5:79676163
|
T | TAC | 7 | a0001c0001t0001g0141a0001c0001t0001g0252a0001c0001t0001g0254others(4): Show | 7 | HG00544.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1209-3390_1209-338 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | |||||
chr5:79676163
|
T | TACAC | 7 | a0001c0001t0005g0126a0001c0001t0019g0131a0001c0001t0019g0132others(4): Show | 7 | HG02486.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1209-3392_1209-338 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | |||||
chr5:79676163
|
T | TACACAC | 30 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0116others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1209-3394_1209-338 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | |||||
chr5:79676163
|
T | TACACACA others(1): Show |
9 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1209-3396_1209-338 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | |||||
chr5:79676163
|
TAC | T | 3 | a0001c0001t0001g0323a0001c0001t0013g0245a0001c0001t0015g0300 | 3 | HG01257.hp1 HG02148.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1209-3390_1209-338 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | |||||
chr5:79676163
|
TACAC | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0273a0001c0001t0001g0281others(1): Show | 4 | HG01891.hp2 HG02071.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209-3392_1209-338 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | |||||
chr5:79676163
|
TACACAC | T | 5 | a0001c0001t0001g0266a0001c0001t0001g0279a0001c0001t0002g0035others(2): Show | 6 | HG01515.hp2 HG01517.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-3394_1209-338 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | |||||
chr5:79676163
|
TACACACA others(1): Show |
T | 103 | a0001c0001t0002g0034a0001c0001t0002g0036a0001c0001t0002g0038others(100): Show | 105 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(102): Show |
intron_variant | MODIFIER | c.1209-3396_1209-338 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | |||||
chr5:79676163
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0022g0078 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1209-3398_1209-338 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | |||||
chr5:79676180
|
A | G | 1 | a0001c0001t0012g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1209-3399A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676180 | ||||||
chr5:79676337
|
G | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-3242G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676337 | ||||||
chr5:79676434
|
A | C | 57 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(54): Show | 57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1209-3145A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676434 | ||||||
chr5:79676631
|
G | C | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-2948G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676631 | ||||||
chr5:79677417
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1209-2162T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677417 | ||||||
chr5:79677709
|
T | C | 34 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(31): Show | 34 | HG00673.hp2 HG02083.hp1 HG02155.hp2 others(31): Show |
intron_variant | MODIFIER | c.1209-1870T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677709 | ||||||
chr5:79677726
|
A | G | 1 | a0001c0001t0021g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1209-1853A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677726 | ||||||
chr5:79677735
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1209-1844C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677735 | ||||||
chr5:79677764
|
T | A | 1 | a0001c0001t0003g0043 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1209-1815T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677764 | ||||||
chr5:79677863
|
G | C | 1 | a0001c0001t0026g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1209-1716G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677863 | ||||||
chr5:79678166
|
C | T | 1 | a0001c0001t0040g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1209-1413C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678166 | ||||||
chr5:79678178
|
G | A | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-1401G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678178 | ||||||
chr5:79678281
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1209-1298A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678281 | ||||||
chr5:79678511
|
G | GA | 42 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1209-1060dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79678511 | |||||
chr5:79678556
|
A | T | 3 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0006g0330 | 3 | HG03041.hp1 NA18955.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1209-1023A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678556 | ||||||
chr5:79678643
|
C | T | 42 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1209-936C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678643 | ||||||
chr5:79678738
|
T | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1209-841T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678738 | ||||||
chr5:79678986
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1209-593A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678986 | ||||||
chr5:79679083
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1209-496T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79679083 | ||||||
chr5:79679085
|
T | C | 31 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1209-494T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79679085 | ||||||
chr5:79679273
|
T | C | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-306T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79679273 | ||||||
chr5:79679374
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1209-205G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79679374 | ||||||
chr5:79679411
|
GA | G | 11 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1209-159delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79679411 | |||||
chr5:79679836
|
A | G | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1300+166A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79679836 | ||||||
chr5:79680487
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1300+817C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680487 | ||||||
chr5:79680573
|
G | A | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300+903G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680573 | ||||||
chr5:79680633
|
G | A | 205 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(202): Show | 208 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1300+963G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680633 | ||||||
chr5:79680772
|
A | G | 2 | a0001c0001t0014g0118a0001c0001t0014g0119 | 2 | HG00099.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1300+1102A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680772 | ||||||
chr5:79680926
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1301-1056G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680926 | ||||||
chr5:79680986
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1301-996T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680986 | ||||||
chr5:79681150
|
A | AT | 136 | a0001c0001t0001g0145a0001c0001t0001g0152a0001c0001t0001g0153others(133): Show | 138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1301-804dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 79681150 | |||||
chr5:79681150
|
A | ATT | 42 | a0001c0001t0001g0231a0001c0001t0001g0301a0001c0001t0001g0306others(39): Show | 42 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1301-805_1301-804d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 79681150 | |||||
chr5:79681150
|
AT | A | 10 | a0001c0001t0001g0154a0001c0001t0001g0310a0001c0001t0006g0004others(7): Show | 11 | HG01243.hp2 HG01943.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1301-804delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 79681150 | |||||
chr5:79681150
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0024g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1301-814_1301-804d others(13): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 79681150 | |||||
chr5:79681246
|
A | G | 2 | a0001c0001t0038g0226a0001c0001t0041g0110 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1301-736A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681246 | ||||||
chr5:79681365
|
G | A | 2 | a0001c0001t0004g0086a0001c0001t0011g0026 | 2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1301-617G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681365 | ||||||
chr5:79681418
|
A | G | 31 | a0001c0001t0005g0111a0001c0001t0005g0114a0001c0001t0005g0115others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1301-564A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681418 | ||||||
chr5:79681456
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1301-526C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681456 | ||||||
chr5:79681649
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0167others(1): Show | 4 | HG01074.hp1 HG01255.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-333C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681649 | ||||||
chr5:79681838
|
A | C | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1301-144A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681838 | ||||||
chr5:79681961
|
C | T | 2 | a0001c0001t0005g0126a0001c0001t0005g0149 | 2 | HG03017.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1301-21C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681961 | ||||||
chr5:79682430
|
C | T | 6 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1380+369C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682430 | ||||||
chr5:79682446
|
A | AT | 27 | a0001c0001t0001g0174a0001c0001t0001g0200a0001c0001t0001g0217others(24): Show | 28 | HG00609.hp2 HG00741.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.1380+404dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79682446 | |||||
chr5:79682566
|
T | C | 2 | a0001c0001t0005g0114a0001c0001t0005g0146 | 2 | HG03831.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1380+505T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682566 | ||||||
chr5:79682683
|
G | A | 2 | a0001c0001t0005g0125a0001c0001t0005g0147 | 2 | NA18949.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1380+622G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682683 | ||||||
chr5:79682744
|
C | T | 3 | a0001c0001t0006g0290a0001c0001t0006g0291a0001c0001t0006g0330 | 3 | HG02886.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1380+683C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682744 | ||||||
chr5:79682775
|
A | G | 107 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(104): Show | 110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1380+714A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682775 | ||||||
chr5:79682806
|
T | C | 4 | a0001c0001t0019g0131a0001c0001t0019g0132a0001c0001t0020g0130others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380+745T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682806 | ||||||
chr5:79682903
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1380+842A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682903 | ||||||
chr5:79682904
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1380+843T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682904 | ||||||
chr5:79682966
|
A | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0213 | 2 | NA18982.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1380+905A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682966 | ||||||
chr5:79683115
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0174 | 2 | HG00609.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1380+1054A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683115 | ||||||
chr5:79683313
|
T | TCA | 17 | a0001c0001t0001g0200a0001c0001t0001g0228a0001c0001t0005g0126others(14): Show | 18 | HG00099.hp2 HG00639.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1380+1280_1380+128 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | |||||
chr5:79683313
|
T | TCACA | 7 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1380+1278_1380+128 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | |||||
chr5:79683313
|
TCA | T | 55 | a0001c0001t0002g0076a0001c0001t0003g0006a0001c0001t0003g0008others(52): Show | 56 | HG01167.hp2 HG01433.hp2 HG01891.hp1 others(53): Show |
intron_variant | MODIFIER | c.1380+1280_1380+128 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | |||||
chr5:79683313
|
TCACA | T | 12 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0079others(9): Show | 12 | HG00140.hp2 HG01928.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1380+1278_1380+128 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | |||||
chr5:79683313
|
TCACACA | T | 53 | a0001c0001t0001g0233a0001c0001t0001g0256a0001c0001t0001g0259others(50): Show | 55 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.1380+1276_1380+128 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | |||||
chr5:79683437
|
G | C | 1 | a0001c0001t0028g0331 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1380+1376G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683437 | ||||||
chr5:79683541
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1380+1480A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683541 | ||||||
chr5:79683565
|
G | A | 35 | a0001c0001t0002g0065a0001c0001t0003g0006a0001c0001t0003g0008others(32): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.1380+1504G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683565 | ||||||
chr5:79683706
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1381-1493G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683706 | ||||||
chr5:79683923
|
C | CA | 41 | a0001c0001t0001g0145a0001c0001t0001g0236a0001c0001t0001g0261others(38): Show | 41 | HG00673.hp1 HG01109.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1381-1247dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
C | CAA | 7 | a0001c0001t0001g0138a0001c0001t0001g0158a0001c0001t0001g0167others(4): Show | 7 | HG01074.hp1 HG01255.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1381-1248_1381-124 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
C | CAAA | 32 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0151others(29): Show | 32 | HG00408.hp2 HG00597.hp2 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.1381-1249_1381-124 others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
C | CAAAA | 20 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0160others(17): Show | 20 | HG00639.hp1 HG01175.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-1250_1381-124 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
C | CAAAAA | 6 | a0001c0001t0001g0135a0001c0001t0001g0152a0001c0001t0001g0183others(3): Show | 6 | HG01243.hp1 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1381-1251_1381-124 others(9): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
CAA | C | 28 | a0001c0001t0002g0061a0001c0001t0002g0076a0001c0001t0002g0087others(25): Show | 28 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1381-1248_1381-124 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
CAAA | C | 76 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0036others(73): Show | 79 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.1381-1249_1381-124 others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0005g0114a0001c0001t0005g0120a0001c0001t0005g0122others(7): Show | 10 | HG00423.hp2 HG00558.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.1381-1254_1381-124 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
CAAAAAAA others(2): Show |
C | 24 | a0001c0001t0005g0111a0001c0001t0005g0115a0001c0001t0005g0116others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1381-1255_1381-124 others(13): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0039g0282 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1381-1256_1381-124 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0266 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1381-1259_1381-124 others(17): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79683923
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0006g0330 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1381-1263_1381-124 others(21): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | |||||
chr5:79684335
|
G | A | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1381-864G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684335 | ||||||
chr5:79684420
|
C | G | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1381-779C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684420 | ||||||
chr5:79684565
|
T | C | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1381-634T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684565 | ||||||
chr5:79684670
|
C | T | 210 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(207): Show | 213 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.1381-529C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684670 | ||||||
chr5:79684857
|
T | C | 300 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139others(297): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1381-342T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684857 | ||||||
chr5:79684869
|
GC | G | 5 | a0001c0001t0021g0112a0001c0001t0021g0113a0001c0001t0038g0226others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1381-329delC | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684869 | ||||||
chr5:79684931
|
G | A | 1 | a0001c0001t0042g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1381-268G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684931 | ||||||
chr5:79684953
|
G | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0216 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1381-246G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684953 |