geneid | 55775 |
---|---|
ensemblid | ENSG00000042088.14 |
hgncid | 18884 |
symbol | TDP1 |
name | tyrosyl-DNA phosphodiesterase 1 |
refseq_nuc | NM_018319.4 |
refseq_prot | NP_060789.2 |
ensembl_nuc | ENST00000335725.9 |
ensembl_prot | ENSP00000337353.4 |
mane_status | MANE Select |
chr | chr14 |
start | 89955927 |
end | 90044764 |
strand | + |
ver | v1.2 |
region | chr14:89955927-90044764 |
region5000 | chr14:89950927-90049764 |
regionname0 | TDP1_chr14_89955927_90044764 |
regionname5000 | TDP1_chr14_89950927_90049764 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 608 | 208 | 58 | 44 | 79 | 4 | 21 | 69 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0002 | 0/0 | 608 | 35 | 25 | 3 | 4 | 0 | 3 | 4 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0003 | 0/0 | 608 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0004 | 0/0 | 608 | 6 | 0 | 6 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0005 | 0/0 | 608 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0006 | 0/0 | 608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0007 | 0/0 | 608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0008 | 0/0 | 608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0009 | 0/0 | 608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1827 | 150 | 15 | 39 | 74 | 3 | 17 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0002 | 0/0 | 1827 | 44 | 29 | 5 | 5 | 1 | 4 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0003 | 0/0 | 1827 | 20 | 13 | 0 | 4 | 0 | 3 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0004 | 0/0 | 1827 | 14 | 11 | 3 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0005 | 0/0 | 1827 | 14 | 14 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0006 | 0/0 | 1827 | 8 | 8 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0007 | 0/0 | 1827 | 6 | 0 | 6 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0008 | 0/0 | 1827 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0009 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0010 | 0/0 | 1827 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0011 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0012 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
c0013 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1896 | 119 | 32 | 29 | 42 | 3 | 12 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0002 | 0/1 | 1896 | 52 | 2 | 14 | 30 | 0 | 5 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0003 | 0/0 | 1896 | 22 | 13 | 1 | 4 | 0 | 4 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0004 | 0/0 | 1895 | 19 | 5 | 4 | 6 | 1 | 3 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0005 | 0/0 | 1897 | 12 | 9 | 3 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0006 | 0/0 | 1896 | 9 | 8 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0007 | 0/0 | 1895 | 8 | 8 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0008 | 0/0 | 1896 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0009 | 0/0 | 1897 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0010 | 0/0 | 1895 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0011 | 0/0 | 1896 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0012 | 0/0 | 1896 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0013 | 0/0 | 1895 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0014 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0015 | 0/0 | 1896 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0016 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0017 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0018 | 0/0 | 1895 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0019 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0020 | 0/0 | 1896 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
t0021 | 0/0 | 1895 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0187 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1827 | 150 | 15 | 39 | 74 | 3 | 17 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002 | 0/0 | 1827 | 44 | 29 | 5 | 5 | 1 | 4 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0005 | 0/0 | 1827 | 14 | 14 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0002c0003 | 0/0 | 1827 | 20 | 13 | 0 | 4 | 0 | 3 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0002c0004 | 0/0 | 1827 | 14 | 11 | 3 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0002c0011 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0003c0006 | 0/0 | 1827 | 8 | 8 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0004c0007 | 0/0 | 1827 | 6 | 0 | 6 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0005c0008 | 0/0 | 1827 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0006c0012 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0007c0010 | 0/0 | 1827 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0008c0009 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0009c0013 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3722 | 100 | 13 | 29 | 42 | 3 | 12 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0001t0002 | 0/1 | 3722 | 46 | 2 | 8 | 30 | 0 | 5 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0001t0011 | 0/0 | 3722 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0001t0015 | 0/0 | 3722 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0001t0020 | 0/0 | 3722 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002t0001 | 0/0 | 3722 | 5 | 5 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002t0003 | 0/0 | 3722 | 2 | 1 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002t0004 | 0/0 | 3721 | 18 | 5 | 4 | 5 | 1 | 3 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002t0006 | 0/0 | 3722 | 9 | 8 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002t0008 | 0/0 | 3722 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002t0010 | 0/0 | 3721 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002t0013 | 0/0 | 3721 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002t0014 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0002t0021 | 0/0 | 3721 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0005t0001 | 0/0 | 3722 | 11 | 11 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0005t0016 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0005t0017 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0001c0005t0018 | 0/0 | 3721 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0002c0003t0003 | 0/0 | 3722 | 19 | 12 | 0 | 4 | 0 | 3 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0002c0003t0012 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0002c0004t0005 | 0/0 | 3723 | 11 | 8 | 3 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0002c0004t0009 | 0/0 | 3723 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0002c0011t0019 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0003c0006t0007 | 0/0 | 3721 | 8 | 8 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0004c0007t0002 | 0/0 | 3722 | 6 | 0 | 6 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0005c0008t0001 | 0/0 | 3722 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0006c0012t0012 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0007c0010t0003 | 0/0 | 3722 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0008c0009t0005 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
a0009c0013t0004 | 0/0 | 3721 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | copy fasta | chr14 | 89950927 | 90049764 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0187 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0011g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0015g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0001t0020g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0013g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0002t0021g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0016g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0017g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0001c0005t0018g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0003t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0004t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0002c0011t0019g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0003c0006t0007g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0003c0006t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0003c0006t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0003c0006t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0003c0006t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0003c0006t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0004c0007t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0004c0007t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0004c0007t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0004c0007t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0004c0007t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0004c0007t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0005c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0005c0008t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0005c0008t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0006c0012t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0007c0010t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0008c0009t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
a0009c0013t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0231 | EUR | FIN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00735 | hp2 | a0002 | c0004 | t0005 | g0075 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01070 | hp2 | a0007 | c0010 | t0003 | g0197 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01081 | hp1 | a0002 | c0004 | t0005 | g0077 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01109 | hp2 | a0002 | c0004 | t0005 | g0086 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01168 | hp2 | a0001 | c0002 | t0004 | g0227 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01169 | hp2 | a0001 | c0002 | t0004 | g0232 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01192 | hp1 | a0001 | c0002 | t0006 | g0237 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01255 | hp1 | a0001 | c0001 | t0020 | g0007 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01256 | hp1 | a0001 | c0002 | t0004 | g0233 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01256 | hp2 | a0004 | c0007 | t0002 | g0040 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01433 | hp1 | a0001 | c0002 | t0004 | g0218 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01433 | hp2 | a0004 | c0007 | t0002 | g0057 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01884 | hp1 | a0003 | c0006 | t0007 | g0002 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01891 | hp2 | a0003 | c0006 | t0007 | g0089 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01943 | hp2 | a0004 | c0007 | t0002 | g0038 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01981 | hp1 | a0004 | c0007 | t0002 | g0061 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01981 | hp2 | a0001 | c0001 | t0015 | g0167 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02055 | hp1 | a0006 | c0012 | t0012 | g0149 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02055 | hp2 | a0002 | c0004 | t0009 | g0081 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0243 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02145 | hp2 | a0002 | c0004 | t0005 | g0082 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CDX | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02257 | hp2 | a0001 | c0005 | t0001 | g0026 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02258 | hp1 | a0001 | c0002 | t0004 | g0221 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02258 | hp2 | a0001 | c0005 | t0001 | g0028 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02273 | hp2 | a0004 | c0007 | t0002 | g0055 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02280 | hp1 | a0001 | c0002 | t0006 | g0241 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02451 | hp1 | a0001 | c0002 | t0004 | g0224 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02451 | hp2 | a0002 | c0003 | t0003 | g0140 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02572 | hp2 | a0001 | c0002 | t0021 | g0204 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02602 | hp2 | a0002 | c0003 | t0003 | g0138 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02615 | hp1 | a0005 | c0008 | t0001 | g0147 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02622 | hp1 | a0001 | c0002 | t0010 | g0245 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02622 | hp2 | a0001 | c0005 | t0018 | g0029 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02630 | hp1 | a0002 | c0004 | t0009 | g0079 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02630 | hp2 | a0001 | c0002 | t0013 | g0211 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02647 | hp2 | a0001 | c0002 | t0014 | g0017 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02717 | hp1 | a0001 | c0002 | t0006 | g0239 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02717 | hp2 | a0001 | c0005 | t0001 | g0004 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02723 | hp2 | a0002 | c0003 | t0012 | g0201 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02738 | hp2 | a0002 | c0003 | t0003 | g0137 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02809 | hp1 | a0002 | c0003 | t0003 | g0139 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02809 | hp2 | a0002 | c0004 | t0005 | g0074 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0242 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02886 | hp2 | a0005 | c0008 | t0001 | g0146 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02896 | hp1 | a0001 | c0002 | t0004 | g0222 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02896 | hp2 | a0003 | c0006 | t0007 | g0090 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02897 | hp1 | a0003 | c0006 | t0007 | g0091 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0220 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02922 | hp2 | a0001 | c0005 | t0001 | g0020 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02965 | hp1 | a0001 | c0002 | t0010 | g0234 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02965 | hp2 | a0001 | c0002 | t0008 | g0209 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02970 | hp1 | a0002 | c0011 | t0019 | g0142 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02970 | hp2 | a0002 | c0004 | t0005 | g0008 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02976 | hp1 | a0008 | c0009 | t0005 | g0083 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02976 | hp2 | a0003 | c0006 | t0007 | g0002 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0205 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03041 | hp2 | a0001 | c0002 | t0006 | g0238 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03098 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03098 | hp2 | a0005 | c0008 | t0001 | g0148 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03130 | hp1 | a0001 | c0002 | t0010 | g0235 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03130 | hp2 | a0002 | c0004 | t0009 | g0080 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03139 | hp2 | a0001 | c0002 | t0006 | g0240 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03195 | hp1 | a0002 | c0003 | t0003 | g0196 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03209 | hp2 | a0002 | c0003 | t0003 | g0200 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03225 | hp1 | a0001 | c0005 | t0001 | g0025 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03225 | hp2 | a0002 | c0003 | t0003 | g0011 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03453 | hp1 | a0001 | c0005 | t0016 | g0027 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03453 | hp2 | a0002 | c0004 | t0005 | g0078 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03486 | hp2 | a0001 | c0005 | t0001 | g0023 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03516 | hp1 | a0002 | c0004 | t0005 | g0076 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03516 | hp2 | a0002 | c0003 | t0003 | g0016 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03540 | hp1 | a0001 | c0002 | t0004 | g0223 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03540 | hp2 | a0002 | c0003 | t0003 | g0145 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03579 | hp1 | a0001 | c0002 | t0008 | g0213 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03579 | hp2 | a0002 | c0003 | t0003 | g0141 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03654 | hp2 | a0002 | c0003 | t0003 | g0144 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0229 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03834 | hp1 | a0001 | c0002 | t0004 | g0230 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | STU | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG04228 | hp1 | a0001 | c0002 | t0004 | g0228 | SAS | STU | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18522 | hp1 | a0001 | c0005 | t0001 | g0022 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18522 | hp2 | a0002 | c0003 | t0003 | g0194 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18906 | hp1 | a0002 | c0004 | t0005 | g0085 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18944 | hp2 | a0001 | c0002 | t0004 | g0216 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18951 | hp2 | a0001 | c0001 | t0011 | g0099 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18957 | hp1 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18968 | hp1 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18973 | hp2 | a0001 | c0002 | t0004 | g0217 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18989 | hp2 | a0001 | c0002 | t0004 | g0219 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19009 | hp2 | a0002 | c0003 | t0003 | g0199 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19030 | hp1 | a0002 | c0004 | t0005 | g0084 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19030 | hp2 | a0002 | c0003 | t0003 | g0143 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19043 | hp1 | a0002 | c0003 | t0003 | g0011 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19043 | hp2 | a0001 | c0005 | t0001 | g0072 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19056 | hp2 | a0001 | c0002 | t0004 | g0225 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19077 | hp2 | a0001 | c0001 | t0011 | g0153 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19083 | hp2 | a0009 | c0013 | t0004 | g0226 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19084 | hp2 | a0001 | c0002 | t0004 | g0215 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19088 | hp1 | a0002 | c0003 | t0003 | g0198 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19240 | hp1 | a0001 | c0005 | t0001 | g0030 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA19240 | hp2 | a0003 | c0006 | t0007 | g0002 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA20129 | hp2 | a0003 | c0006 | t0007 | g0088 | AFR | ASW | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | GIH | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | GIH | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG01123 | hp2 | a0004 | c0007 | t0002 | g0056 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02109 | hp2 | a0001 | c0005 | t0001 | g0024 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02486 | hp1 | a0001 | c0005 | t0017 | g0021 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02486 | hp2 | a0001 | c0002 | t0013 | g0210 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02559 | hp1 | a0002 | c0003 | t0003 | g0195 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03471 | hp1 | a0001 | c0002 | t0006 | g0244 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG03471 | hp2 | a0002 | c0004 | t0005 | g0008 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG06807 | hp1 | a0003 | c0006 | t0007 | g0087 | AFR | USA | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
HG06807 | hp2 | a0001 | c0002 | t0006 | g0236 | AFR | USA | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA20300 | hp1 | a0001 | c0002 | t0008 | g0214 | AFR | USA | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | USA | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0049 | REF | REF | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0187 | REF | REF | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:89963150
|
A | G | 1 | a0009 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.36A>G | p.Ile12Met | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 310/3722 | 36/1827 | 12/608 | chr14 | 89963150 | ||
chr14:89963399
|
G | T | 1 | a0005 | 3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.285G>T | p.Glu95Asp | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 559/3722 | 285/1827 | 95/608 | chr14 | 89963399 | ||
chr14:89963416
|
C | T | 1 | a0004 | 6 | HG01123.hp2 HG01256.hp2 HG01433.hp2 others(3): Show |
missense_variant | MODERATE | c.302C>T | p.Pro101Leu | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 576/3722 | 302/1827 | 101/608 | chr14 | 89963416 | ||
chr14:89963514
|
G | A | 4 | a0002a0003a0007others(1): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
missense_variant | MODERATE | c.400G>A | p.Ala134Thr | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 674/3722 | 400/1827 | 134/608 | chr14 | 89963514 | ||
chr14:89984542
|
G | A | 2 | a0003a0006 | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
missense_variant | MODERATE | c.911G>A | p.Arg304Gln | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/17 | 1185/3722 | 911/1827 | 304/608 | chr14 | 89984542 | ||
chr14:89988938
|
G | A | 1 | a0008 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1165G>A | p.Ala389Thr | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/17 | 1439/3722 | 1165/1827 | 389/608 | chr14 | 89988938 | ||
chr14:89989085
|
T | A | 1 | a0007 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.1312T>A | p.Tyr438Asn | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/17 | 1586/3722 | 1312/1827 | 438/608 | chr14 | 89989085 | ||
chr14:90033166
|
A | G | 1 | a0003 | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
missense_variant | MODERATE | c.1705A>G | p.Thr569Ala | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/17 | 1979/3722 | 1705/1827 | 569/608 | chr14 | 90033166 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:89963357
|
C | G | 1 | a0006c0012 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.243C>G | p.Ser81Ser | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 517/3722 | 243/1827 | 81/608 | chr14 | 89963357 | ||
chr14:89963405
|
A | G | 10 | a0001c0002a0001c0005a0002c0003others(7): Show | 105 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(102): Show |
synonymous_variant | LOW | c.291A>G | p.Gln97Gln | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 565/3722 | 291/1827 | 97/608 | chr14 | 89963405 | ||
chr14:89963651
|
C | T | 1 | a0005c0008 | 3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.537C>T | p.Asn179Asn | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 811/3722 | 537/1827 | 179/608 | chr14 | 89963651 | ||
chr14:89985156
|
A | G | 3 | a0002c0003a0002c0011a0007c0010 | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
synonymous_variant | LOW | c.1077A>G | p.Pro359Pro | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/17 | 1351/3722 | 1077/1827 | 359/608 | chr14 | 89985156 | ||
chr14:89985177
|
A | G | 2 | a0003c0006a0006c0012 | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
synonymous_variant | LOW | c.1098A>G | p.Gln366Gln | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/17 | 1372/3722 | 1098/1827 | 366/608 | chr14 | 89985177 | ||
chr14:89985186
|
T | C | 1 | a0001c0005 | 14 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
synonymous_variant | LOW | c.1107T>C | p.Asn369Asn | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/17 | 1381/3722 | 1107/1827 | 369/608 | chr14 | 89985186 | ||
chr14:89993478
|
C | T | 1 | a0006c0012 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1536C>T | p.Val512Val | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/17 | 1810/3722 | 1536/1827 | 512/608 | chr14 | 89993478 | ||
chr14:90043116
|
G | A | 1 | a0002c0011 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1800G>A | p.Thr600Thr | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 2074/3722 | 1800/1827 | 600/608 | chr14 | 90043116 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:89956584
|
A | G | 4 | a0001c0002t0004a0001c0002t0010a0001c0002t0021others(1): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-224A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/17 | 6531 | chr14 | 89956584 | |||||
chr14:89956631
|
C | T | 4 | a0002c0004t0005a0002c0004t0009a0003c0006t0007others(1): Show | 23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-177C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/17 | 6484 | chr14 | 89956631 | |||||
chr14:89956787
|
C | T | 3 | a0001c0001t0002a0001c0001t0020a0004c0007t0002 | 53 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(50): Show |
5_prime_UTR_variant | MODIFIER | c.-21C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/17 | 6328 | chr14 | 89956787 | |||||
chr14:90043220
|
C | T | 18 | a0001c0001t0011a0001c0002t0003a0001c0002t0004others(15): Show | 87 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 77 | chr14 | 90043220 | |||||
chr14:90043230
|
T | TAA | 3 | a0002c0004t0005a0002c0004t0009a0008c0009t0005 | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*89_*90dupAA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 91 | INFO_REALIGN_3_PRIME | chr14 | 90043230 | ||||
chr14:90043536
|
T | C | 3 | a0001c0001t0011a0001c0002t0004a0009c0013t0004 | 21 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*393T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 393 | chr14 | 90043536 | |||||
chr14:90043682
|
G | A | 1 | a0001c0002t0006 | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*539G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 539 | chr14 | 90043682 | |||||
chr14:90043741
|
G | A | 1 | a0003c0006t0007 | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*598G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 598 | chr14 | 90043741 | |||||
chr14:90043748
|
CA | C | 10 | a0001c0002t0004a0001c0002t0010a0001c0002t0013others(7): Show | 49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*608delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 608 | INFO_REALIGN_3_PRIME | chr14 | 90043748 | ||||
chr14:90043810
|
G | T | 1 | a0001c0005t0017 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*667G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 667 | chr14 | 90043810 | |||||
chr14:90043942
|
A | G | 3 | a0001c0002t0008a0001c0005t0016a0002c0004t0009 | 7 | HG02055.hp2 HG02630.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*799A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 799 | chr14 | 90043942 | |||||
chr14:90044075
|
C | T | 1 | a0001c0002t0013 | 2 | HG02486.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*932C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 932 | chr14 | 90044075 | |||||
chr14:90044248
|
A | G | 1 | a0001c0002t0021 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1105A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1105 | chr14 | 90044248 | |||||
chr14:90044293
|
G | A | 1 | a0001c0002t0014 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1150G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1150 | chr14 | 90044293 | |||||
chr14:90044475
|
G | A | 1 | a0002c0011t0019 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1332G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1332 | chr14 | 90044475 | |||||
chr14:90044489
|
G | A | 1 | a0001c0001t0020 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1346 | chr14 | 90044489 | |||||
chr14:90044591
|
G | A | 7 | a0001c0002t0004a0001c0002t0010a0001c0002t0013others(4): Show | 27 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1448G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1448 | chr14 | 90044591 | |||||
chr14:90044595
|
C | T | 7 | a0001c0002t0004a0001c0002t0010a0001c0002t0013others(4): Show | 27 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1452C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1452 | chr14 | 90044595 | |||||
chr14:90044603
|
C | G | 7 | a0001c0002t0004a0001c0002t0010a0001c0002t0013others(4): Show | 27 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1460C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1460 | chr14 | 90044603 | |||||
chr14:90044733
|
C | T | 1 | a0001c0001t0015 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1590C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1590 | chr14 | 90044733 | |||||
chr14:90044761
|
T | C | 1 | a0001c0002t0013 | 2 | HG02486.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1618T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1618 | chr14 | 90044761 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:89955983
|
C | A | 1 | a0001c0002t0003g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-231+13C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89955983 | ||||||
chr14:89956020
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-231+50C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956020 | ||||||
chr14:89956034
|
G | A | 1 | a0002c0003t0003g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-231+64G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956034 | ||||||
chr14:89956038
|
T | G | 64 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(61): Show | 70 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.-231+68T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956038 | ||||||
chr14:89956052
|
G | A | 20 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(17): Show | 23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-231+82G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956052 | ||||||
chr14:89956053
|
A | G | 126 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(123): Show | 135 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(132): Show |
intron_variant | MODIFIER | c.-231+83A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956053 | ||||||
chr14:89956202
|
G | C | 1 | a0001c0002t0021g0204 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-231+232G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956202 | ||||||
chr14:89956320
|
T | C | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0092others(44): Show | 49 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-230-258T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956320 | ||||||
chr14:89956395
|
C | G | 1 | a0001c0002t0010g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-230-183C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956395 | ||||||
chr14:89956470
|
A | G | 1 | a0001c0002t0006g0244 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-230-108A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956470 | ||||||
chr14:89956527
|
C | T | 126 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(123): Show | 135 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(132): Show |
intron_variant | MODIFIER | c.-230-51C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956527 | ||||||
chr14:89956564
|
C | A | 126 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(123): Show | 135 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(132): Show |
intron_variant | MODIFIER | c.-230-14C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956564 | ||||||
chr14:89956574
|
G | T | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.-230-4G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956574 | ||||||
chr14:89956828
|
CAG | C | 23 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(20): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8+33_-8+34delAG | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr14 | 89956828 | |||||
chr14:89957064
|
C | T | 1 | a0001c0002t0010g0235 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-8+264C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957064 | ||||||
chr14:89957065
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8+265G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957065 | ||||||
chr14:89957383
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-8+583A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957383 | ||||||
chr14:89957392
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8+592T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957392 | ||||||
chr14:89957450
|
A | T | 2 | a0001c0002t0008g0213a0001c0002t0008g0214 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-8+650A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957450 | ||||||
chr14:89957459
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-8+659C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957459 | ||||||
chr14:89957515
|
G | A | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-8+715G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957515 | ||||||
chr14:89957546
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8+746C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957546 | ||||||
chr14:89957579
|
G | A | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+779G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957579 | ||||||
chr14:89957837
|
C | A | 11 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(8): Show | 12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+1037C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957837 | ||||||
chr14:89957855
|
C | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8+1055C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957855 | ||||||
chr14:89957946
|
C | T | 22 | a0001c0002t0008g0213a0001c0002t0008g0214a0002c0004t0005g0008others(19): Show | 25 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+1146C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957946 | ||||||
chr14:89957986
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+1186G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957986 | ||||||
chr14:89957988
|
G | A | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-8+1188G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957988 | ||||||
chr14:89958124
|
G | A | 9 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+1324G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958124 | ||||||
chr14:89958274
|
A | C | 30 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8+1474A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958274 | ||||||
chr14:89958306
|
A | G | 1 | a0001c0001t0001g0003 | 3 | HG01884.hp2 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-8+1506A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958306 | ||||||
chr14:89958332
|
G | C | 196 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0092others(193): Show | 209 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.-8+1532G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958332 | ||||||
chr14:89958361
|
G | A | 23 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(20): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8+1561G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958361 | ||||||
chr14:89958369
|
G | A | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+1569G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958369 | ||||||
chr14:89958393
|
C | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8+1593C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958393 | ||||||
chr14:89958510
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-8+1710T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958510 | ||||||
chr14:89958557
|
T | A | 2 | a0005c0008t0001g0146a0005c0008t0001g0147 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-8+1757T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958557 | ||||||
chr14:89958674
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-8+1874A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958674 | ||||||
chr14:89958703
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-8+1903A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958703 | ||||||
chr14:89958735
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-8+1935C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958735 | ||||||
chr14:89958820
|
C | T | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+2020C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958820 | ||||||
chr14:89958828
|
C | T | 2 | a0001c0001t0001g0192a0001c0005t0001g0072 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-8+2028C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958828 | ||||||
chr14:89958847
|
A | G | 2 | a0001c0002t0003g0205a0006c0012t0012g0149 | 2 | HG02055.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-8+2047A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958847 | ||||||
chr14:89959123
|
TC | T | 3 | a0005c0008t0001g0146a0005c0008t0001g0147a0005c0008t0001g0148 | 3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-8+2324delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959123 | ||||||
chr14:89959140
|
G | A | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-8+2340G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959140 | ||||||
chr14:89959353
|
C | T | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-8+2553C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959353 | ||||||
chr14:89959504
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8+2704C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959504 | ||||||
chr14:89959539
|
G | A | 1 | a0002c0003t0003g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-8+2739G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959539 | ||||||
chr14:89959836
|
T | C | 6 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(3): Show | 6 | HG00408.hp2 NA18947.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+3036T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959836 | ||||||
chr14:89960023
|
G | C | 1 | a0001c0005t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-3085G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960023 | ||||||
chr14:89960259
|
A | G | 1 | a0001c0002t0001g0212 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-2849A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960259 | ||||||
chr14:89960276
|
T | G | 1 | a0001c0002t0008g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-7-2832T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960276 | ||||||
chr14:89960300
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7-2808A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960300 | ||||||
chr14:89960421
|
T | C | 6 | a0002c0003t0003g0014a0002c0003t0003g0195a0002c0003t0003g0196others(3): Show | 7 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-2687T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960421 | ||||||
chr14:89960503
|
C | T | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-7-2605C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960503 | ||||||
chr14:89960639
|
A | G | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-2469A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960639 | ||||||
chr14:89960747
|
T | C | 98 | a0001c0002t0001g0031a0001c0002t0001g0206a0001c0002t0001g0207others(95): Show | 104 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.-7-2361T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960747 | ||||||
chr14:89960863
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-2245C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960863 | ||||||
chr14:89960872
|
C | T | 2 | a0001c0002t0008g0213a0001c0002t0008g0214 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-7-2236C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960872 | ||||||
chr14:89960957
|
G | A | 2 | a0002c0003t0003g0137a0002c0003t0003g0138 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-7-2151G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960957 | ||||||
chr14:89961074
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0003g0015 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-7-2034C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961074 | ||||||
chr14:89961115
|
C | T | 4 | a0001c0005t0001g0004a0001c0005t0001g0028a0001c0005t0001g0030others(1): Show | 5 | HG02258.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-1993C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961115 | ||||||
chr14:89961124
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-1984G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961124 | ||||||
chr14:89961157
|
G | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-7-1951G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961157 | ||||||
chr14:89961191
|
T | A | 5 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0139others(2): Show | 6 | HG02451.hp2 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-1917T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961191 | ||||||
chr14:89961478
|
A | G | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7-1630A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961478 | ||||||
chr14:89961551
|
A | G | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-7-1557A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961551 | ||||||
chr14:89961605
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.-7-1503G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961605 | ||||||
chr14:89961648
|
C | A | 1 | a0003c0006t0007g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-7-1460C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961648 | ||||||
chr14:89961763
|
T | C | 2 | a0002c0003t0003g0194a0002c0003t0003g0200 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-7-1345T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961763 | ||||||
chr14:89961774
|
T | A | 65 | a0001c0002t0003g0205a0001c0002t0004g0215a0001c0002t0004g0216others(62): Show | 70 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-7-1334T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961774 | ||||||
chr14:89961879
|
C | T | 3 | a0002c0003t0003g0014a0002c0003t0003g0198a0002c0003t0003g0199 | 4 | NA18957.hp1 NA18968.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-1229C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961879 | ||||||
chr14:89961911
|
G | A | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-1197G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961911 | ||||||
chr14:89962041
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-7-1067A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962041 | ||||||
chr14:89962074
|
G | A | 5 | a0002c0003t0003g0137a0002c0003t0003g0138a0002c0003t0003g0143others(2): Show | 5 | HG02602.hp2 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-1034G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962074 | ||||||
chr14:89962090
|
A | G | 32 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(29): Show | 32 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-7-1018A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962090 | ||||||
chr14:89962613
|
C | T | 2 | a0001c0002t0010g0234a0001c0002t0021g0204 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-7-495C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962613 | ||||||
chr14:89962667
|
C | T | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-441C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962667 | ||||||
chr14:89962712
|
G | GA | 33 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(30): Show | 37 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7-386dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr14 | 89962712 | |||||
chr14:89962759
|
C | T | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-349C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962759 | ||||||
chr14:89962773
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-7-335G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962773 | ||||||
chr14:89962826
|
T | C | 73 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(70): Show | 78 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.-7-282T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962826 | ||||||
chr14:89962884
|
A | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-224A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962884 | ||||||
chr14:89962954
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-7-154A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962954 | ||||||
chr14:89963016
|
G | A | 1 | a0001c0002t0006g0244 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-7-92G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89963016 | ||||||
chr14:89963771
|
C | G | 2 | a0001c0002t0013g0210a0001c0002t0013g0211 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.559+98C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89963771 | ||||||
chr14:89963787
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.559+114A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89963787 | ||||||
chr14:89964020
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.559+347A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964020 | ||||||
chr14:89964114
|
G | C | 1 | a0001c0001t0002g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.559+441G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964114 | ||||||
chr14:89964207
|
AGAAG | A | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.559+535_559+538del others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964207 | ||||||
chr14:89964226
|
T | C | 20 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(17): Show | 23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+553T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964226 | ||||||
chr14:89964340
|
C | T | 1 | a0001c0002t0004g0233 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.559+667C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964340 | ||||||
chr14:89964782
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.559+1109C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964782 | ||||||
chr14:89964828
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00642.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.559+1155A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964828 | ||||||
chr14:89964894
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.559+1221A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964894 | ||||||
chr14:89964898
|
T | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.559+1225T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964898 | ||||||
chr14:89964928
|
T | C | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.560-1219T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964928 | ||||||
chr14:89965010
|
G | T | 1 | a0001c0001t0002g0070 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.560-1137G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965010 | ||||||
chr14:89965165
|
A | G | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.560-982A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965165 | ||||||
chr14:89965194
|
G | T | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560-953G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965194 | ||||||
chr14:89965265
|
G | GC | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.560-880dupC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr14 | 89965265 | |||||
chr14:89965344
|
CTG | C | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.560-801_560-800del others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr14 | 89965344 | |||||
chr14:89965361
|
T | G | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.560-786T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965361 | ||||||
chr14:89965397
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.560-750C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965397 | ||||||
chr14:89965504
|
A | G | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.560-643A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965504 | ||||||
chr14:89965893
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560-254A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965893 | ||||||
chr14:89965921
|
G | A | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.560-226G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965921 | ||||||
chr14:89966082
|
G | A | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.560-65G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89966082 | ||||||
chr14:89966106
|
T | C | 1 | a0002c0004t0005g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.560-41T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89966106 | ||||||
chr14:89966271
|
C | T | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.603+81C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966271 | ||||||
chr14:89966308
|
A | G | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.603+118A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966308 | ||||||
chr14:89966492
|
A | T | 2 | a0003c0006t0007g0090a0003c0006t0007g0091 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.603+302A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966492 | ||||||
chr14:89966547
|
G | A | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.603+357G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966547 | ||||||
chr14:89966665
|
A | G | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.603+475A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966665 | ||||||
chr14:89966669
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.603+479G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966669 | ||||||
chr14:89966670
|
T | C | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.603+480T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966670 | ||||||
chr14:89966693
|
C | T | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.603+503C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966693 | ||||||
chr14:89967259
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.604-108G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89967259 | ||||||
chr14:89967575
|
G | A | 1 | a0002c0004t0005g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.659+153G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89967575 | ||||||
chr14:89967760
|
G | A | 2 | a0001c0002t0001g0031a0001c0002t0003g0015 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.659+338G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89967760 | ||||||
chr14:89967779
|
C | T | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.659+357C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89967779 | ||||||
chr14:89967954
|
C | CAGTG | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.659+534_659+535ins others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89967954 | |||||
chr14:89968001
|
C | T | 20 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(17): Show | 23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.659+579C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968001 | ||||||
chr14:89968006
|
C | T | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.659+584C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968006 | ||||||
chr14:89968113
|
T | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.659+691T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968113 | ||||||
chr14:89968160
|
C | CT | 11 | a0001c0001t0002g0069a0001c0002t0006g0236a0001c0002t0006g0237others(8): Show | 11 | HG01192.hp1 HG01928.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.659+754dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89968160 | |||||
chr14:89968160
|
CTT | C | 39 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(36): Show | 44 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.659+753_659+754del others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89968160 | |||||
chr14:89968195
|
T | C | 2 | a0001c0002t0001g0206a0001c0002t0001g0207 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.659+773T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968195 | ||||||
chr14:89968264
|
G | C | 30 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(27): Show | 32 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.659+842G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968264 | ||||||
chr14:89968332
|
C | T | 26 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(23): Show | 30 | HG01070.hp2 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.659+910C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968332 | ||||||
chr14:89968370
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.659+948A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968370 | ||||||
chr14:89968424
|
A | G | 40 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(37): Show | 45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.659+1002A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968424 | ||||||
chr14:89968492
|
A | G | 99 | a0001c0002t0001g0031a0001c0002t0001g0206a0001c0002t0001g0207others(96): Show | 105 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(102): Show |
intron_variant | MODIFIER | c.659+1070A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968492 | ||||||
chr14:89968574
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.659+1152T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968574 | ||||||
chr14:89968660
|
G | C | 5 | a0002c0003t0003g0137a0002c0003t0003g0138a0002c0003t0003g0143others(2): Show | 5 | HG02602.hp2 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.659+1238G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968660 | ||||||
chr14:89968719
|
A | G | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.659+1297A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968719 | ||||||
chr14:89968861
|
T | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.659+1439T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968861 | ||||||
chr14:89969277
|
CCTT | C | 23 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(20): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.659+1858_659+1860d others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969277 | |||||
chr14:89969304
|
A | C | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.660-1871A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969304 | ||||||
chr14:89969313
|
TG | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-1859delG | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969313 | |||||
chr14:89969487
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.660-1688A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969487 | ||||||
chr14:89969569
|
G | A | 246 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(243): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.660-1606G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969569 | ||||||
chr14:89969580
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.660-1595G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969580 | ||||||
chr14:89969581
|
T | A | 64 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(61): Show | 69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.660-1594T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969581 | ||||||
chr14:89969714
|
A | G | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-1461A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969714 | ||||||
chr14:89969833
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.660-1342A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969833 | ||||||
chr14:89969876
|
C | CT | 162 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(159): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.660-1281dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969876 | |||||
chr14:89969876
|
C | CTT | 39 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0186others(36): Show | 39 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.660-1282_660-1281d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969876 | |||||
chr14:89969876
|
CT | C | 15 | a0002c0003t0003g0145a0002c0004t0005g0008a0002c0004t0005g0074others(12): Show | 16 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.660-1281delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969876 | |||||
chr14:89969881
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.660-1294T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969881 | ||||||
chr14:89969887
|
T | C | 1 | a0003c0006t0007g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.660-1288T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969887 | ||||||
chr14:89969898
|
G | A | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-1277G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969898 | ||||||
chr14:89969907
|
C | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.660-1268C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969907 | ||||||
chr14:89969915
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.660-1260C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969915 | ||||||
chr14:89969946
|
G | A | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.660-1229G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969946 | ||||||
chr14:89970033
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.660-1142C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970033 | ||||||
chr14:89970078
|
G | A | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.660-1097G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970078 | ||||||
chr14:89970118
|
T | C | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-1057T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970118 | ||||||
chr14:89970171
|
T | C | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-1004T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970171 | ||||||
chr14:89970224
|
A | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-951A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970224 | ||||||
chr14:89970235
|
A | G | 1 | a0001c0005t0016g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.660-940A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970235 | ||||||
chr14:89970308
|
C | T | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-867C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970308 | ||||||
chr14:89970313
|
C | T | 1 | a0001c0002t0006g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.660-862C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970313 | ||||||
chr14:89970485
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0105 | 3 | NA18954.hp1 NA18968.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.660-690A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970485 | ||||||
chr14:89970580
|
G | A | 2 | a0001c0002t0008g0213a0001c0002t0008g0214 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.660-595G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970580 | ||||||
chr14:89970580
|
G | C | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.660-595G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970580 | ||||||
chr14:89970741
|
A | G | 2 | a0002c0004t0005g0008a0002c0004t0005g0086 | 3 | HG01109.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.660-434A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970741 | ||||||
chr14:89970797
|
C | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-378C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970797 | ||||||
chr14:89970798
|
G | A | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-377G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970798 | ||||||
chr14:89970821
|
A | G | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.660-354A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970821 | ||||||
chr14:89970834
|
T | A | 134 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0001g0108others(131): Show | 143 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.660-341T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970834 | ||||||
chr14:89970838
|
T | A | 32 | a0001c0001t0002g0034a0001c0002t0001g0031a0001c0002t0001g0206others(29): Show | 34 | HG01074.hp1 HG01433.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.660-337T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970838 | ||||||
chr14:89970901
|
C | A | 5 | a0002c0003t0003g0137a0002c0003t0003g0138a0002c0003t0003g0143others(2): Show | 5 | HG02602.hp2 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.660-274C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970901 | ||||||
chr14:89970926
|
C | T | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-249C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970926 | ||||||
chr14:89970957
|
G | C | 1 | a0001c0001t0002g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.660-218G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970957 | ||||||
chr14:89970984
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.660-191C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970984 | ||||||
chr14:89971013
|
A | T | 11 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(8): Show | 12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.660-162A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89971013 | ||||||
chr14:89971072
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-103G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89971072 | ||||||
chr14:89971312
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.756+41G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971312 | ||||||
chr14:89971367
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.756+96T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971367 | ||||||
chr14:89971399
|
T | C | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+128T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971399 | ||||||
chr14:89971418
|
T | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0064 | 2 | NA19004.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.756+147T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971418 | ||||||
chr14:89971511
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.756+240T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971511 | ||||||
chr14:89971536
|
G | C | 11 | a0001c0005t0001g0004a0001c0005t0001g0020a0001c0005t0001g0022others(8): Show | 12 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.756+265G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971536 | ||||||
chr14:89971862
|
T | A | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+591T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971862 | ||||||
chr14:89971865
|
T | C | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+594T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971865 | ||||||
chr14:89971911
|
CT | C | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+649delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89971911 | |||||
chr14:89971947
|
C | T | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.756+676C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971947 | ||||||
chr14:89971974
|
G | T | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.756+703G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971974 | ||||||
chr14:89971985
|
A | G | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+714A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971985 | ||||||
chr14:89972041
|
T | C | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.756+770T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972041 | ||||||
chr14:89972232
|
A | G | 2 | a0001c0002t0013g0210a0001c0002t0013g0211 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.756+961A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972232 | ||||||
chr14:89972252
|
G | C | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+981G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972252 | ||||||
chr14:89972276
|
C | T | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+1005C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972276 | ||||||
chr14:89972293
|
G | GAA | 198 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0092others(195): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.756+1023_756+1024i others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89972293 | |||||
chr14:89972345
|
T | A | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+1074T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972345 | ||||||
chr14:89972536
|
CT | C | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+1268delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89972536 | |||||
chr14:89972554
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+1283A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972554 | ||||||
chr14:89972563
|
G | A | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+1292G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972563 | ||||||
chr14:89972604
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+1333A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972604 | ||||||
chr14:89972617
|
ATCTTCTA others(7): Show |
A | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.756+1348_756+1361d others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89972617 | |||||
chr14:89972636
|
G | A | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+1365G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972636 | ||||||
chr14:89972794
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.756+1523T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972794 | ||||||
chr14:89972841
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.756+1570G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972841 | ||||||
chr14:89973042
|
A | T | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.756+1771A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973042 | ||||||
chr14:89973065
|
G | GT | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.756+1797dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89973065 | |||||
chr14:89973189
|
C | A | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.756+1918C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973189 | ||||||
chr14:89973256
|
A | G | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.756+1985A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973256 | ||||||
chr14:89973282
|
G | A | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+2011G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973282 | ||||||
chr14:89973364
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.756+2093T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973364 | ||||||
chr14:89973458
|
A | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+2187A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973458 | ||||||
chr14:89973473
|
A | T | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+2202A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973473 | ||||||
chr14:89973607
|
C | T | 9 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.757-2174C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973607 | ||||||
chr14:89973706
|
G | A | 38 | a0001c0002t0001g0031a0001c0002t0003g0015a0001c0002t0004g0215others(35): Show | 39 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.757-2075G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973706 | ||||||
chr14:89973736
|
G | A | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-2045G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973736 | ||||||
chr14:89973821
|
T | C | 38 | a0001c0002t0001g0031a0001c0002t0003g0015a0001c0002t0004g0215others(35): Show | 39 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.757-1960T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973821 | ||||||
chr14:89973880
|
C | CTTA | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG01074.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.757-1899_757-1897d others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89973880 | |||||
chr14:89973894
|
C | T | 3 | a0002c0003t0003g0137a0002c0003t0003g0138a0002c0003t0003g0144 | 3 | HG02602.hp2 HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.757-1887C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973894 | ||||||
chr14:89973896
|
T | C | 9 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.757-1885T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973896 | ||||||
chr14:89973939
|
A | G | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-1842A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973939 | ||||||
chr14:89973951
|
G | A | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-1830G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973951 | ||||||
chr14:89973966
|
G | A | 3 | a0002c0004t0005g0076a0002c0004t0005g0077a0002c0004t0005g0078 | 3 | HG01081.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.757-1815G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973966 | ||||||
chr14:89973979
|
G | A | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.757-1802G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973979 | ||||||
chr14:89974232
|
G | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.757-1549G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974232 | ||||||
chr14:89974246
|
A | C | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-1535A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974246 | ||||||
chr14:89974316
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG01109.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.757-1465C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974316 | ||||||
chr14:89974317
|
G | T | 150 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(147): Show | 161 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(158): Show |
intron_variant | MODIFIER | c.757-1464G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974317 | ||||||
chr14:89974584
|
G | A | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.757-1197G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974584 | ||||||
chr14:89974622
|
G | A | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.757-1159G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974622 | ||||||
chr14:89974637
|
ATTGCATG others(10): Show |
A | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.757-1139_757-1123d others(19): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89974637 | |||||
chr14:89974799
|
A | G | 79 | a0001c0002t0001g0031a0001c0002t0003g0015a0001c0002t0004g0215others(76): Show | 85 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.757-982A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974799 | ||||||
chr14:89975015
|
A | G | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.757-766A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975015 | ||||||
chr14:89975098
|
C | T | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.757-683C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975098 | ||||||
chr14:89975106
|
C | T | 1 | a0002c0004t0005g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.757-675C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975106 | ||||||
chr14:89975168
|
T | C | 33 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(30): Show | 36 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.757-613T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975168 | ||||||
chr14:89975200
|
T | C | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.757-581T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975200 | ||||||
chr14:89975240
|
A | G | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-541A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975240 | ||||||
chr14:89975311
|
C | T | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-470C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975311 | ||||||
chr14:89975532
|
T | TGTA | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.757-245_757-243dup others(3): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975532 | |||||
chr14:89975577
|
T | TTG | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.757-200_757-199dup others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975577 | |||||
chr14:89975581
|
G | GT | 10 | a0001c0001t0001g0127a0001c0001t0002g0062a0001c0002t0006g0236others(7): Show | 10 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.757-180dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975581 | |||||
chr14:89975581
|
GT | G | 45 | a0001c0001t0001g0111a0001c0001t0002g0036a0001c0001t0002g0037others(42): Show | 48 | HG00323.hp1 HG00323.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.757-180delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975581 | |||||
chr14:89975581
|
GTT | G | 21 | a0001c0002t0004g0227a0002c0003t0003g0011a0002c0003t0003g0014others(18): Show | 23 | HG01070.hp2 HG01168.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.757-181_757-180del others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975581 | |||||
chr14:89975585
|
T | G | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.757-196T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975585 | ||||||
chr14:89975587
|
T | G | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.757-194T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975587 | ||||||
chr14:89975682
|
T | A | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.757-99T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975682 | ||||||
chr14:89975719
|
T | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01123.hp1 HG01175.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.757-62T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975719 | ||||||
chr14:89975853
|
A | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+38A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975853 | ||||||
chr14:89975867
|
A | G | 35 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(32): Show | 38 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.791+52A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975867 | ||||||
chr14:89975873
|
C | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.791+58C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975873 | ||||||
chr14:89975882
|
T | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.791+67T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975882 | ||||||
chr14:89975970
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+155C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975970 | ||||||
chr14:89976117
|
A | G | 2 | a0001c0002t0004g0227a0001c0002t0004g0232 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.791+302A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976117 | ||||||
chr14:89976210
|
A | ATCC | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+399_791+401dup others(3): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976210 | |||||
chr14:89976231
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.791+416G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976231 | ||||||
chr14:89976251
|
A | G | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+436A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976251 | ||||||
chr14:89976255
|
G | A | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.791+440G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976255 | ||||||
chr14:89976375
|
C | T | 5 | a0001c0002t0008g0213a0001c0002t0008g0214a0003c0006t0007g0089others(2): Show | 5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.791+560C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976375 | ||||||
chr14:89976527
|
C | CT | 53 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(50): Show | 54 | HG01081.hp2 HG01109.hp1 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.791+740dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | |||||
chr14:89976527
|
C | CTT | 7 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0136others(4): Show | 7 | HG01123.hp1 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.791+739_791+740dup others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | |||||
chr14:89976527
|
CT | C | 23 | a0001c0001t0001g0111a0001c0001t0001g0150a0001c0001t0001g0189others(20): Show | 23 | HG00323.hp1 HG01168.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.791+740delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | |||||
chr14:89976527
|
CTTTTTTT others(3): Show |
C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+731_791+740del others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | |||||
chr14:89976527
|
CTTTTTTT others(4): Show |
C | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.791+730_791+740del others(11): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | |||||
chr14:89976543
|
T | A | 1 | a0002c0003t0003g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.791+728T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976543 | ||||||
chr14:89976543
|
T | TA | 7 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(4): Show | 8 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.791+728_791+729ins others(1): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976543 | ||||||
chr14:89976554
|
T | TTTTTTTT others(3): Show |
1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.791+740_791+741ins others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976554 | |||||
chr14:89976555
|
T | A | 9 | a0001c0001t0001g0113a0002c0003t0003g0014a0002c0003t0003g0194others(6): Show | 10 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.791+740T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976555 | ||||||
chr14:89976555
|
T | TA | 11 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(8): Show | 12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.791+741dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976555 | |||||
chr14:89976567
|
C | T | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.791+752C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976567 | ||||||
chr14:89976606
|
G | A | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.791+791G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976606 | ||||||
chr14:89976704
|
CTT | C | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.791+892_791+893del others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976704 | |||||
chr14:89977128
|
T | C | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+1313T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977128 | ||||||
chr14:89977184
|
A | G | 1 | a0001c0002t0010g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.791+1369A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977184 | ||||||
chr14:89977190
|
G | A | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.791+1375G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977190 | ||||||
chr14:89977208
|
A | T | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+1393A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977208 | ||||||
chr14:89977304
|
A | T | 4 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(1): Show | 4 | HG01891.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.791+1489A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977304 | ||||||
chr14:89977305
|
T | A | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+1490T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977305 | ||||||
chr14:89977339
|
C | T | 1 | a0001c0001t0001g0009 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.791+1524C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977339 | ||||||
chr14:89977358
|
C | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.791+1543C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977358 | ||||||
chr14:89977442
|
C | T | 34 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(31): Show | 37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+1627C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977442 | ||||||
chr14:89977443
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.791+1628G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977443 | ||||||
chr14:89977487
|
G | A | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.791+1672G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977487 | ||||||
chr14:89977544
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+1729C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977544 | ||||||
chr14:89977590
|
A | G | 35 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(32): Show | 38 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.791+1775A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977590 | ||||||
chr14:89977605
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.791+1790A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977605 | ||||||
chr14:89977634
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.791+1819T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977634 | ||||||
chr14:89977644
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.791+1829A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977644 | ||||||
chr14:89977975
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.791+2160G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977975 | ||||||
chr14:89978133
|
G | A | 1 | a0001c0005t0001g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.791+2318G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978133 | ||||||
chr14:89978143
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.791+2328C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978143 | ||||||
chr14:89978148
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.791+2333C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978148 | ||||||
chr14:89978154
|
A | G | 41 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(38): Show | 46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.791+2339A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978154 | ||||||
chr14:89978212
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-2328A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978212 | ||||||
chr14:89978262
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.792-2278C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978262 | ||||||
chr14:89978310
|
A | G | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.792-2230A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978310 | ||||||
chr14:89978330
|
C | A | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.792-2210C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978330 | ||||||
chr14:89978351
|
T | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.792-2189T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978351 | ||||||
chr14:89978366
|
C | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.792-2174C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978366 | ||||||
chr14:89978438
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.792-2102T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978438 | ||||||
chr14:89978464
|
A | G | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.792-2076A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978464 | ||||||
chr14:89978602
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1938C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978602 | ||||||
chr14:89978671
|
C | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.792-1869C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978671 | ||||||
chr14:89978961
|
CT | C | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1574delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89978961 | |||||
chr14:89978968
|
T | TCGAACTC others(101): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1572_792-1571i others(110): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978968 | ||||||
chr14:89978975
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1565T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978975 | ||||||
chr14:89978981
|
A | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1559A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978981 | ||||||
chr14:89978985
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1555T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978985 | ||||||
chr14:89978988
|
C | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1552C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978988 | ||||||
chr14:89978990
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1550T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978990 | ||||||
chr14:89978991
|
C | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1549C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978991 | ||||||
chr14:89978993
|
T | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1547T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978993 | ||||||
chr14:89978996
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1544C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978996 | ||||||
chr14:89979003
|
A | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1537A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979003 | ||||||
chr14:89979005
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1535G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979005 | ||||||
chr14:89979009
|
A | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1531A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979009 | ||||||
chr14:89979012
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1528T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979012 | ||||||
chr14:89979014
|
G | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1526G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979014 | ||||||
chr14:89979018
|
A | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1522A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979018 | ||||||
chr14:89979023
|
G | GTGAGAGA others(99): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1517_792-1516i others(108): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979023 | ||||||
chr14:89979025
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1515G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979025 | ||||||
chr14:89979138
|
G | A | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.792-1402G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979138 | ||||||
chr14:89979186
|
A | G | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.792-1354A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979186 | ||||||
chr14:89979219
|
G | A | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1321G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979219 | ||||||
chr14:89979261
|
G | A | 1 | a0001c0005t0016g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.792-1279G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979261 | ||||||
chr14:89979312
|
ATT | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1214_792-1213d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89979312 | |||||
chr14:89979342
|
C | T | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1198C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979342 | ||||||
chr14:89979403
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1137A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979403 | ||||||
chr14:89979461
|
G | C | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1079G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979461 | ||||||
chr14:89979598
|
C | G | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-942C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979598 | ||||||
chr14:89979762
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-778C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979762 | ||||||
chr14:89979835
|
G | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.792-705G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979835 | ||||||
chr14:89980048
|
A | G | 23 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(20): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.792-492A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980048 | ||||||
chr14:89980058
|
G | A | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.792-482G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980058 | ||||||
chr14:89980225
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.792-315G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980225 | ||||||
chr14:89980245
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-295A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980245 | ||||||
chr14:89980394
|
A | G | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.792-146A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980394 | ||||||
chr14:89980425
|
G | A | 2 | a0003c0006t0007g0090a0003c0006t0007g0091 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.792-115G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980425 | ||||||
chr14:89980459
|
A | G | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-81A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980459 | ||||||
chr14:89980488
|
A | G | 11 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(8): Show | 12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.792-52A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980488 | ||||||
chr14:89980664
|
G | C | 1 | a0001c0001t0011g0153 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.884+32G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89980664 | ||||||
chr14:89980687
|
G | C | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.884+55G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89980687 | ||||||
chr14:89980716
|
A | AT | 28 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(25): Show | 32 | HG01070.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.884+94dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr14 | 89980716 | |||||
chr14:89980958
|
G | C | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+326G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89980958 | ||||||
chr14:89981022
|
A | G | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.884+390A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981022 | ||||||
chr14:89981155
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.884+523A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981155 | ||||||
chr14:89981184
|
G | A | 2 | a0001c0002t0004g0228a0001c0002t0004g0229 | 2 | HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.884+552G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981184 | ||||||
chr14:89981292
|
A | G | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.884+660A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981292 | ||||||
chr14:89981406
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+774C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981406 | ||||||
chr14:89981510
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.884+878C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981510 | ||||||
chr14:89981534
|
C | T | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.884+902C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981534 | ||||||
chr14:89981784
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1152C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981784 | ||||||
chr14:89981854
|
T | C | 1 | a0001c0002t0008g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.884+1222T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981854 | ||||||
chr14:89981893
|
C | CCAAGGCT others(19): Show |
7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1265_884+1266i others(28): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr14 | 89981893 | |||||
chr14:89981909
|
C | T | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.884+1277C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981909 | ||||||
chr14:89981950
|
C | T | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.884+1318C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981950 | ||||||
chr14:89981992
|
C | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0203 | 3 | HG01081.hp2 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.884+1360C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981992 | ||||||
chr14:89982000
|
T | C | 50 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(47): Show | 55 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.884+1368T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982000 | ||||||
chr14:89982047
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1415A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982047 | ||||||
chr14:89982148
|
A | G | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1516A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982148 | ||||||
chr14:89982190
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1558C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982190 | ||||||
chr14:89982197
|
A | G | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1565A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982197 | ||||||
chr14:89982237
|
G | A | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.884+1605G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982237 | ||||||
chr14:89982334
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.884+1702A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982334 | ||||||
chr14:89982364
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1732A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982364 | ||||||
chr14:89982468
|
A | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.884+1836A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982468 | ||||||
chr14:89982654
|
T | TA | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.885-1855dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr14 | 89982654 | |||||
chr14:89982724
|
A | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.885-1792A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982724 | ||||||
chr14:89982790
|
T | G | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1726T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982790 | ||||||
chr14:89982794
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1722C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982794 | ||||||
chr14:89982880
|
A | G | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1636A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982880 | ||||||
chr14:89982907
|
G | T | 23 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(20): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.885-1609G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982907 | ||||||
chr14:89982932
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1584A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982932 | ||||||
chr14:89983117
|
T | C | 7 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(4): Show | 8 | HG00735.hp2 HG01109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.885-1399T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983117 | ||||||
chr14:89983147
|
G | C | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1369G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983147 | ||||||
chr14:89983206
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1310G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983206 | ||||||
chr14:89983302
|
C | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.885-1214C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983302 | ||||||
chr14:89983428
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1088C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983428 | ||||||
chr14:89983549
|
C | T | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.885-967C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983549 | ||||||
chr14:89983593
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.885-923T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983593 | ||||||
chr14:89983765
|
A | G | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.885-751A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983765 | ||||||
chr14:89983779
|
A | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.885-737A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983779 | ||||||
chr14:89983789
|
T | C | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.885-727T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983789 | ||||||
chr14:89983923
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0132 | 3 | HG00639.hp2 HG00738.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.885-593T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983923 | ||||||
chr14:89984022
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0186 | 2 | NA18982.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.885-494A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984022 | ||||||
chr14:89984063
|
T | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.885-453T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984063 | ||||||
chr14:89984143
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.885-373C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984143 | ||||||
chr14:89984145
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-371G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984145 | ||||||
chr14:89984217
|
C | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-299C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984217 | ||||||
chr14:89984280
|
G | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0132 | 3 | HG00639.hp2 HG00738.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.885-236G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984280 | ||||||
chr14:89984298
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.885-218A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984298 | ||||||
chr14:89984345
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-171A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984345 | ||||||
chr14:89984365
|
T | G | 74 | a0001c0002t0003g0205a0001c0002t0004g0215a0001c0002t0004g0216others(71): Show | 79 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.885-151T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984365 | ||||||
chr14:89984501
|
T | C | 1 | a0001c0002t0008g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.885-15T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984501 | ||||||
chr14:89984862
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1052+179A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984862 | ||||||
chr14:89984863
|
G | A | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1052+180G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984863 | ||||||
chr14:89984885
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1052+202G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984885 | ||||||
chr14:89984889
|
A | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1052+206A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984889 | ||||||
chr14:89984923
|
T | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1053-209T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984923 | ||||||
chr14:89984959
|
A | G | 246 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(243): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.1053-173A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984959 | ||||||
chr14:89985069
|
A | AT | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1053-55dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr14 | 89985069 | |||||
chr14:89985242
|
A | T | 1 | a0001c0001t0002g0058 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1131+32A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985242 | ||||||
chr14:89985247
|
A | T | 1 | a0005c0008t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1131+37A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985247 | ||||||
chr14:89985248
|
T | A | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1131+38T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985248 | ||||||
chr14:89985391
|
CTT | C | 10 | a0001c0005t0001g0004a0001c0005t0001g0020a0001c0005t0001g0022others(7): Show | 11 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1131+184_1131+185d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr14 | 89985391 | |||||
chr14:89985520
|
A | T | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1131+310A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985520 | ||||||
chr14:89985553
|
GA | G | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+347delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr14 | 89985553 | |||||
chr14:89985571
|
C | T | 9 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1131+361C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985571 | ||||||
chr14:89985722
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+512G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985722 | ||||||
chr14:89985736
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+526A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985736 | ||||||
chr14:89985767
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+557G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985767 | ||||||
chr14:89985780
|
GC | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131+571delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985780 | ||||||
chr14:89985825
|
A | C | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131+615A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985825 | ||||||
chr14:89985838
|
C | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | NA18989.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1131+628C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985838 | ||||||
chr14:89985959
|
G | A | 3 | a0001c0002t0010g0234a0001c0002t0010g0245a0001c0002t0021g0204 | 3 | HG02572.hp2 HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1131+749G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985959 | ||||||
chr14:89986223
|
A | C | 1 | a0007c0010t0003g0197 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1131+1013A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986223 | ||||||
chr14:89986232
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1131+1022G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986232 | ||||||
chr14:89986246
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1131+1036T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986246 | ||||||
chr14:89986300
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+1090G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986300 | ||||||
chr14:89986309
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+1099C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986309 | ||||||
chr14:89986332
|
G | A | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1131+1122G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986332 | ||||||
chr14:89986399
|
T | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1131+1189T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986399 | ||||||
chr14:89986406
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1131+1196T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986406 | ||||||
chr14:89986664
|
A | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1131+1454A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986664 | ||||||
chr14:89986669
|
C | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1131+1459C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986669 | ||||||
chr14:89986698
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131+1488G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986698 | ||||||
chr14:89986733
|
T | A | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1131+1523T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986733 | ||||||
chr14:89986780
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1131+1570A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986780 | ||||||
chr14:89986831
|
C | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+1621C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986831 | ||||||
chr14:89986848
|
A | AATAC | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+1642_1131+164 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr14 | 89986848 | |||||
chr14:89986909
|
T | C | 1 | a0001c0005t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1131+1699T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986909 | ||||||
chr14:89986993
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1131+1783T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986993 | ||||||
chr14:89987297
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132-1608G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987297 | ||||||
chr14:89987303
|
C | T | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1132-1602C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987303 | ||||||
chr14:89987406
|
T | G | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1132-1499T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987406 | ||||||
chr14:89987475
|
C | T | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1132-1430C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987475 | ||||||
chr14:89987491
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-1414G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987491 | ||||||
chr14:89987724
|
T | A | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1132-1181T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987724 | ||||||
chr14:89987847
|
T | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-1058T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987847 | ||||||
chr14:89987876
|
AT | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-1021delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr14 | 89987876 | |||||
chr14:89987921
|
G | A | 3 | a0001c0001t0002g0001a0001c0001t0002g0036a0001c0001t0002g0065 | 6 | NA18970.hp1 NA18972.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132-984G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987921 | ||||||
chr14:89988251
|
T | C | 3 | a0005c0008t0001g0146a0005c0008t0001g0147a0005c0008t0001g0148 | 3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1132-654T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988251 | ||||||
chr14:89988421
|
G | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-484G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988421 | ||||||
chr14:89988459
|
T | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-446T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988459 | ||||||
chr14:89988695
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1132-210C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988695 | ||||||
chr14:89988762
|
T | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0101others(1): Show | 4 | HG02602.hp1 HG02698.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132-143T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988762 | ||||||
chr14:89989101
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1317+11G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989101 | ||||||
chr14:89989116
|
G | A | 64 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(61): Show | 69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1317+26G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989116 | ||||||
chr14:89989154
|
T | G | 1 | a0001c0005t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1317+64T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989154 | ||||||
chr14:89989169
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1317+79A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989169 | ||||||
chr14:89989195
|
C | CT | 15 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(12): Show | 16 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1317+118dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr14 | 89989195 | |||||
chr14:89989195
|
CT | C | 14 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(11): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1317+118delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr14 | 89989195 | |||||
chr14:89989217
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1317+127G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989217 | ||||||
chr14:89989279
|
C | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1317+189C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989279 | ||||||
chr14:89989328
|
C | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1317+238C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989328 | ||||||
chr14:89989444
|
A | C | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318-273A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989444 | ||||||
chr14:89989459
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1318-258T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989459 | ||||||
chr14:89989510
|
T | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318-207T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989510 | ||||||
chr14:89989554
|
A | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1318-163A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989554 | ||||||
chr14:89989642
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318-75C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989642 | ||||||
chr14:89989687
|
C | T | 15 | a0001c0001t0001g0181a0002c0004t0005g0008a0002c0004t0005g0074others(12): Show | 16 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1318-30C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989687 | ||||||
chr14:89989811
|
A | T | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1366+46A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89989811 | ||||||
chr14:89989843
|
C | G | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1366+78C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89989843 | ||||||
chr14:89989844
|
G | T | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0092others(196): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1366+79G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89989844 | ||||||
chr14:89989883
|
A | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0105 | 3 | NA18954.hp1 NA18968.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1366+118A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89989883 | ||||||
chr14:89990027
|
A | G | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1366+262A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990027 | ||||||
chr14:89990030
|
T | C | 9 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1366+265T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990030 | ||||||
chr14:89990086
|
A | G | 4 | a0001c0002t0006g0238a0001c0002t0006g0239a0001c0002t0006g0240others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+321A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990086 | ||||||
chr14:89990181
|
C | T | 6 | a0002c0003t0003g0014a0002c0003t0003g0195a0002c0003t0003g0196others(3): Show | 7 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366+416C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990181 | ||||||
chr14:89990241
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366+476T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990241 | ||||||
chr14:89990288
|
G | T | 1 | a0001c0001t0002g0039 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1366+523G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990288 | ||||||
chr14:89990331
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366+566A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990331 | ||||||
chr14:89990416
|
C | T | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1366+651C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990416 | ||||||
chr14:89990430
|
T | C | 85 | a0001c0002t0001g0031a0001c0002t0001g0206a0001c0002t0001g0207others(82): Show | 90 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1366+665T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990430 | ||||||
chr14:89990451
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366+686C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990451 | ||||||
chr14:89990547
|
C | CT | 8 | a0001c0001t0001g0111a0001c0002t0001g0206a0002c0003t0003g0011others(5): Show | 9 | HG00323.hp1 HG01070.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1366+805dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | |||||
chr14:89990547
|
CT | C | 32 | a0001c0001t0001g0092a0001c0001t0001g0102a0001c0001t0001g0103others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1366+805delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | |||||
chr14:89990547
|
CTT | C | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1366+804_1366+805d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | |||||
chr14:89990547
|
CTTT | C | 13 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(10): Show | 14 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1366+803_1366+805d others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | |||||
chr14:89990547
|
CTTTTT | C | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366+801_1366+805d others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | |||||
chr14:89990618
|
G | T | 2 | a0001c0002t0001g0031a0001c0002t0003g0015 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1366+853G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990618 | ||||||
chr14:89990794
|
G | C | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1366+1029G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990794 | ||||||
chr14:89991435
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1367-482T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89991435 | ||||||
chr14:89991469
|
C | CAGG | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367-446_1367-445i others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89991469 | |||||
chr14:89991632
|
A | T | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1367-285A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89991632 | ||||||
chr14:89991716
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1367-201C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89991716 | ||||||
chr14:89991839
|
T | A | 16 | a0001c0002t0008g0213a0001c0002t0008g0214a0002c0004t0005g0008others(13): Show | 17 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1367-78T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89991839 | ||||||
chr14:89992053
|
GT | G | 83 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(80): Show | 88 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.1433+81delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr14 | 89992053 | |||||
chr14:89992216
|
G | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1433+233G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992216 | ||||||
chr14:89992365
|
T | A | 85 | a0001c0002t0001g0031a0001c0002t0001g0206a0001c0002t0001g0207others(82): Show | 90 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1433+382T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992365 | ||||||
chr14:89992682
|
A | C | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434-694A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992682 | ||||||
chr14:89992876
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434-500A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992876 | ||||||
chr14:89992911
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1434-465G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992911 | ||||||
chr14:89993014
|
A | G | 23 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(20): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1434-362A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993014 | ||||||
chr14:89993031
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG02109.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1434-345T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993031 | ||||||
chr14:89993067
|
A | T | 1 | a0001c0002t0013g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1434-309A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993067 | ||||||
chr14:89993129
|
A | G | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1434-247A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993129 | ||||||
chr14:89993200
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434-176C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993200 | ||||||
chr14:89993225
|
T | C | 64 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(61): Show | 69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1434-151T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993225 | ||||||
chr14:89993226
|
G | A | 1 | a0002c0011t0019g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1434-150G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993226 | ||||||
chr14:89993343
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434-33A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993343 | ||||||
chr14:89993850
|
T | C | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+367T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89993850 | ||||||
chr14:89993910
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+427G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89993910 | ||||||
chr14:89994086
|
GA | G | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1541+607delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89994086 | |||||
chr14:89994128
|
C | G | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+645C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994128 | ||||||
chr14:89994144
|
T | C | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+661T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994144 | ||||||
chr14:89994259
|
C | T | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+776C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994259 | ||||||
chr14:89994263
|
C | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+780C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994263 | ||||||
chr14:89994293
|
T | G | 1 | a0001c0002t0004g0225 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1541+810T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994293 | ||||||
chr14:89994305
|
C | T | 6 | a0004c0007t0002g0038a0004c0007t0002g0040a0004c0007t0002g0055others(3): Show | 6 | HG01123.hp2 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1541+822C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994305 | ||||||
chr14:89994526
|
G | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+1043G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994526 | ||||||
chr14:89994787
|
T | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+1304T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994787 | ||||||
chr14:89994879
|
A | T | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+1396A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994879 | ||||||
chr14:89994992
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1541+1509G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994992 | ||||||
chr14:89995217
|
T | C | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+1734T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995217 | ||||||
chr14:89995325
|
G | C | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+1842G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995325 | ||||||
chr14:89995347
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1541+1864G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995347 | ||||||
chr14:89995392
|
GC | G | 86 | a0001c0002t0001g0031a0001c0002t0001g0206a0001c0002t0001g0207others(83): Show | 91 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.1541+1914delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89995392 | |||||
chr14:89995485
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2002C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995485 | ||||||
chr14:89995493
|
AAG | A | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1541+2013_1541+201 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89995493 | |||||
chr14:89995494
|
A | C | 37 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(34): Show | 38 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1541+2011A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995494 | ||||||
chr14:89995608
|
A | C | 37 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(34): Show | 38 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1541+2125A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995608 | ||||||
chr14:89995629
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2146A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995629 | ||||||
chr14:89995846
|
A | G | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2363A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995846 | ||||||
chr14:89995982
|
A | C | 56 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(53): Show | 60 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.1541+2499A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995982 | ||||||
chr14:89996022
|
G | A | 74 | a0001c0002t0003g0205a0001c0002t0004g0215a0001c0002t0004g0216others(71): Show | 79 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.1541+2539G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996022 | ||||||
chr14:89996053
|
A | G | 9 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1541+2570A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996053 | ||||||
chr14:89996076
|
C | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+2593C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996076 | ||||||
chr14:89996094
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2611C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996094 | ||||||
chr14:89996241
|
G | A | 1 | a0002c0003t0003g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1541+2758G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996241 | ||||||
chr14:89996242
|
T | C | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2759T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996242 | ||||||
chr14:89996260
|
A | G | 1 | a0003c0006t0007g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1541+2777A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996260 | ||||||
chr14:89996281
|
A | T | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+2798A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996281 | ||||||
chr14:89996526
|
A | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+3043A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996526 | ||||||
chr14:89996620
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+3137G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996620 | ||||||
chr14:89996930
|
C | T | 5 | a0001c0005t0001g0022a0001c0005t0001g0023a0001c0005t0001g0024others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1541+3447C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996930 | ||||||
chr14:89996961
|
T | C | 4 | a0001c0002t0006g0238a0001c0002t0006g0239a0001c0002t0006g0240others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1541+3478T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996961 | ||||||
chr14:89996996
|
A | C | 37 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(34): Show | 38 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1541+3513A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996996 | ||||||
chr14:89997076
|
G | A | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1541+3593G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997076 | ||||||
chr14:89997278
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0042 | 2 | NA18952.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1541+3795G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997278 | ||||||
chr14:89997357
|
T | C | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1541+3874T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997357 | ||||||
chr14:89997358
|
G | C | 2 | a0001c0002t0001g0031a0001c0002t0003g0015 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1541+3875G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997358 | ||||||
chr14:89997394
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+3911A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997394 | ||||||
chr14:89997598
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0101a0001c0001t0001g0157 | 3 | HG02698.hp1 HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1541+4115G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997598 | ||||||
chr14:89997812
|
TTA | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4339_1541+434 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89997812 | |||||
chr14:89997882
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4399A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997882 | ||||||
chr14:89997938
|
CT | C | 65 | a0001c0002t0003g0205a0001c0002t0004g0215a0001c0002t0004g0216others(62): Show | 70 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.1541+4459delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89997938 | |||||
chr14:89997982
|
G | A | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+4499G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997982 | ||||||
chr14:89997990
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4507G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997990 | ||||||
chr14:89998157
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4674C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998157 | ||||||
chr14:89998200
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4717C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998200 | ||||||
chr14:89998201
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4718C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998201 | ||||||
chr14:89998370
|
CAT | C | 5 | a0001c0002t0004g0218a0001c0002t0004g0224a0001c0002t0004g0227others(2): Show | 5 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541+4888_1541+488 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998370 | ||||||
chr14:89998370
|
CATTA | C | 3 | a0001c0002t0004g0215a0001c0002t0004g0220a0001c0002t0004g0221 | 3 | HG02258.hp1 HG02897.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1541+4888_1541+489 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998370 | ||||||
chr14:89998370
|
CATTATA | C | 3 | a0001c0002t0004g0222a0001c0002t0004g0223a0001c0002t0004g0233 | 3 | HG01256.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1541+4888_1541+489 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998370 | ||||||
chr14:89998370
|
CATTATAT others(13): Show |
C | 1 | a0001c0002t0021g0204 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1541+4888_1541+490 others(24): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998370 | ||||||
chr14:89998371
|
A | T | 11 | a0001c0002t0004g0216a0001c0002t0004g0217a0001c0002t0004g0219others(8): Show | 11 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1541+4888A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998371 | ||||||
chr14:89998372
|
T | A | 11 | a0001c0002t0004g0216a0001c0002t0004g0217a0001c0002t0004g0219others(8): Show | 11 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1541+4889T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998372 | ||||||
chr14:89998372
|
T | TTA | 6 | a0001c0001t0001g0010a0001c0001t0001g0103a0001c0002t0008g0213others(3): Show | 7 | HG01081.hp1 HG01255.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541+4939_1541+494 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
T | TTATA | 3 | a0001c0001t0002g0043a0001c0002t0008g0214a0001c0005t0001g0030 | 3 | HG02165.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1541+4937_1541+494 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
T | TTATATA | 3 | a0001c0001t0001g0107a0001c0005t0001g0020a0002c0004t0005g0076 | 3 | HG00280.hp2 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1541+4935_1541+494 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
T | TTATATAT others(3): Show |
1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1541+4931_1541+494 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
T | TTTTATAT others(5): Show |
1 | a0001c0002t0006g0240 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1541+4890_1541+489 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTA | T | 8 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0162others(5): Show | 9 | HG02257.hp1 HG02280.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4939_1541+494 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATA | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0109others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1541+4937_1541+494 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATA | T | 14 | a0001c0001t0001g0093a0001c0001t0001g0133a0001c0001t0001g0134others(11): Show | 14 | HG01255.hp1 HG01934.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1541+4935_1541+494 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(1): Show |
T | 26 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0098others(23): Show | 32 | HG00280.hp1 HG00642.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1541+4933_1541+494 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(3): Show |
T | 16 | a0001c0001t0001g0118a0001c0001t0001g0121a0001c0001t0001g0126others(13): Show | 16 | HG00408.hp1 HG00738.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1541+4931_1541+494 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(5): Show |
T | 18 | a0001c0001t0001g0102a0001c0001t0001g0110a0001c0001t0001g0122others(15): Show | 19 | HG00408.hp2 HG00735.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1541+4929_1541+494 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(7): Show |
T | 8 | a0001c0001t0001g0012a0001c0001t0001g0158a0001c0001t0001g0168others(5): Show | 9 | HG01981.hp2 HG02280.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4927_1541+494 others(18): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(9): Show |
T | 14 | a0001c0001t0001g0097a0001c0001t0001g0116a0001c0001t0001g0150others(11): Show | 14 | HG01928.hp1 HG02602.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.1541+4925_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(11): Show |
T | 16 | a0001c0001t0001g0013a0001c0001t0001g0159a0001c0001t0001g0160others(13): Show | 17 | HG01081.hp2 HG01943.hp1 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1541+4923_1541+494 others(22): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(13): Show |
T | 6 | a0001c0001t0002g0001a0001c0001t0002g0036a0001c0001t0002g0042others(3): Show | 9 | HG01070.hp2 HG02723.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1541+4921_1541+494 others(24): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(15): Show |
T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1541+4919_1541+494 others(26): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0001g0125 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1541+4915_1541+494 others(30): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(21): Show |
T | 3 | a0005c0008t0001g0146a0005c0008t0001g0147a0005c0008t0001g0148 | 3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1541+4913_1541+494 others(32): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(25): Show |
T | 1 | a0001c0001t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1541+4909_1541+494 others(36): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998372
|
TTATATAT others(27): Show |
T | 1 | a0001c0005t0016g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1541+4907_1541+494 others(38): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | |||||
chr14:89998374
|
A | T | 4 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(1): Show | 4 | HG01192.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1541+4891A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998374 | ||||||
chr14:89998376
|
A | T | 1 | a0001c0002t0006g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1541+4893A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998376 | ||||||
chr14:89998384
|
ATATATAT others(37): Show |
A | 2 | a0002c0004t0005g0008a0002c0004t0005g0086 | 3 | HG01109.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1541+4905_1541+494 others(48): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998384 | |||||
chr14:89998388
|
A | T | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+4905A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998388 | ||||||
chr14:89998396
|
A | ATG | 3 | a0001c0002t0004g0219a0001c0002t0010g0235a0009c0013t0004g0226 | 3 | HG03130.hp1 NA18989.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1541+4914_1541+491 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998396 | |||||
chr14:89998396
|
A | G | 1 | a0001c0002t0008g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1541+4913A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998396 | ||||||
chr14:89998400
|
A | G | 6 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0224others(3): Show | 6 | HG01433.hp1 HG02451.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1541+4917A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998400 | ||||||
chr14:89998404
|
A | G | 10 | a0001c0002t0004g0216a0001c0002t0004g0217a0001c0002t0004g0218others(7): Show | 10 | HG00323.hp2 HG01433.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1541+4921A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998404 | ||||||
chr14:89998408
|
A | G | 27 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(24): Show | 29 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1541+4925A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998408 | ||||||
chr14:89998408
|
ATATATAT others(9): Show |
A | 1 | a0001c0002t0008g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1541+4929_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998408 | |||||
chr14:89998412
|
A | G | 33 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(30): Show | 36 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.1541+4929A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998412 | ||||||
chr14:89998412
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1541+4933_1541+494 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998412 | |||||
chr14:89998412
|
ATATATAT others(9): Show |
A | 3 | a0002c0004t0009g0079a0002c0004t0009g0080a0002c0004t0009g0081 | 3 | HG02055.hp2 HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1541+4933_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998412 | |||||
chr14:89998414
|
A | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+4931A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998414 | ||||||
chr14:89998416
|
A | ATATATAT others(11): Show |
2 | a0001c0002t0001g0207a0001c0002t0013g0211 | 2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1541+4940_1541+494 others(22): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998416 | |||||
chr14:89998416
|
A | ATATATAT others(9): Show |
1 | a0001c0002t0013g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998416 | |||||
chr14:89998416
|
A | ATATGTAT others(9): Show |
1 | a0002c0003t0003g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1541+4936_1541+493 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998416 | |||||
chr14:89998416
|
A | ATGTATGT others(3): Show |
1 | a0001c0005t0018g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1541+4934_1541+493 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998416 | |||||
chr14:89998416
|
A | G | 40 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(37): Show | 44 | HG00323.hp2 HG01070.hp2 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.1541+4933A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998416 | ||||||
chr14:89998418
|
ATATATG | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0120a0001c0001t0011g0099 | 3 | HG02132.hp1 NA18951.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1541+4939_1541+494 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998418 | |||||
chr14:89998418
|
ATATATGT others(3): Show |
A | 1 | a0002c0004t0005g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1541+4939_1541+494 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998418 | |||||
chr14:89998420
|
A | ATATATAT others(19): Show |
1 | a0001c0002t0001g0212 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(30): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | ATATATAT others(15): Show |
1 | a0001c0005t0017g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(26): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | ATATATAT others(9): Show |
1 | a0001c0005t0001g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | ATATATAT others(9): Show |
1 | a0002c0011t0019g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | ATATATAT others(13): Show |
1 | a0002c0003t0003g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(24): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | ATATATAT others(17): Show |
1 | a0002c0003t0003g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(28): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | ATATATGT others(7): Show |
1 | a0002c0003t0003g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(18): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | ATATGTAT others(5): Show |
1 | a0001c0002t0006g0236 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1541+4949_1541+496 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | ATATGTAT others(9): Show |
2 | a0001c0002t0006g0244a0002c0003t0003g0144 | 2 | HG03471.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1541+4945_1541+496 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | ATGTATGT others(3): Show |
1 | a0001c0002t0006g0237 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1541+4938_1541+493 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | |||||
chr14:89998420
|
A | G | 63 | a0001c0001t0001g0104a0001c0001t0001g0172a0001c0001t0001g0179others(60): Show | 67 | HG00323.hp2 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.1541+4937A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998420 | ||||||
chr14:89998422
|
ATG | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0119a0001c0002t0003g0205others(1): Show | 4 | HG00735.hp2 HG03017.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1541+4941_1541+494 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998422 | |||||
chr14:89998424
|
G | A | 12 | a0001c0002t0001g0207a0001c0002t0013g0210a0001c0002t0013g0211others(9): Show | 12 | HG01081.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1541+4941G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998424 | ||||||
chr14:89998424
|
G | GTATGTAT others(5): Show |
1 | a0001c0002t0001g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1541+4948_1541+494 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998424 | |||||
chr14:89998428
|
G | A | 11 | a0001c0001t0001g0100a0001c0002t0001g0208a0001c0002t0001g0212others(8): Show | 11 | HG00735.hp2 HG01081.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1541+4945G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998428 | ||||||
chr14:89998432
|
G | A | 7 | a0001c0002t0001g0208a0001c0002t0001g0212a0002c0004t0005g0076others(4): Show | 7 | HG01081.hp1 HG03209.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541+4949G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998432 | ||||||
chr14:89998435
|
T | C | 9 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(6): Show | 10 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1541+4952T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998435 | ||||||
chr14:89998436
|
G | GTATGTAT others(19): Show |
1 | a0002c0003t0003g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1541+4960_1541+496 others(30): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998436 | |||||
chr14:89998436
|
G | GTATGTAT others(31): Show |
1 | a0002c0003t0003g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1541+4960_1541+496 others(42): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998436 | |||||
chr14:89998439
|
T | C | 5 | a0002c0004t0005g0076a0002c0004t0005g0077a0002c0004t0005g0078others(2): Show | 5 | HG01081.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1541+4956T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998439 | ||||||
chr14:89998440
|
GTA | G | 10 | a0001c0005t0001g0023a0002c0004t0005g0008a0002c0004t0005g0074others(7): Show | 11 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1541+4961_1541+496 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998440 | |||||
chr14:89998442
|
A | ATG | 7 | a0001c0002t0001g0208a0001c0002t0001g0212a0002c0004t0005g0076others(4): Show | 7 | HG01081.hp1 HG03209.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541+4960_1541+496 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998442 | |||||
chr14:89998467
|
TATTA | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4988_1541+499 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998467 | |||||
chr14:89998503
|
G | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+5020G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998503 | ||||||
chr14:89998740
|
C | T | 1 | a0002c0003t0003g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1541+5257C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998740 | ||||||
chr14:89998823
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1541+5340G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998823 | ||||||
chr14:89998857
|
G | T | 1 | a0001c0002t0004g0231 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1541+5374G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998857 | ||||||
chr14:89998884
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1541+5401C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998884 | ||||||
chr14:89998901
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+5418C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998901 | ||||||
chr14:89998927
|
G | A | 2 | a0001c0002t0001g0206a0001c0002t0001g0207 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1541+5444G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998927 | ||||||
chr14:89999048
|
A | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+5565A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999048 | ||||||
chr14:89999201
|
G | GA | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+5725dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89999201 | |||||
chr14:89999258
|
A | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+5775A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999258 | ||||||
chr14:89999280
|
A | G | 48 | a0001c0001t0001g0127a0001c0001t0002g0001a0001c0001t0002g0005others(45): Show | 53 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.1541+5797A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999280 | ||||||
chr14:89999295
|
C | T | 2 | a0001c0002t0013g0210a0001c0002t0013g0211 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1541+5812C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999295 | ||||||
chr14:89999463
|
G | T | 1 | a0001c0001t0002g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1541+5980G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999463 | ||||||
chr14:89999576
|
G | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6093G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999576 | ||||||
chr14:89999658
|
A | G | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+6175A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999658 | ||||||
chr14:89999695
|
C | T | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6212C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999695 | ||||||
chr14:89999707
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6224A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999707 | ||||||
chr14:89999708
|
A | G | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+6225A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999708 | ||||||
chr14:89999711
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6228G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999711 | ||||||
chr14:89999786
|
C | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+6303C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999786 | ||||||
chr14:89999811
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6328A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999811 | ||||||
chr14:89999826
|
A | G | 2 | a0001c0002t0006g0238a0001c0002t0006g0241 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1541+6343A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999826 | ||||||
chr14:89999852
|
C | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+6369C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999852 | ||||||
chr14:90000023
|
C | T | 2 | a0001c0002t0013g0210a0001c0002t0013g0211 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1541+6540C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000023 | ||||||
chr14:90000058
|
A | G | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6575A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000058 | ||||||
chr14:90000076
|
C | T | 1 | a0001c0002t0008g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1541+6593C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000076 | ||||||
chr14:90000180
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+6697A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000180 | ||||||
chr14:90000251
|
G | A | 27 | a0001c0002t0006g0238a0001c0002t0006g0239a0001c0002t0006g0240others(24): Show | 30 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1541+6768G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000251 | ||||||
chr14:90000270
|
T | TAGTC | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6788_1541+678 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90000270 | |||||
chr14:90000306
|
T | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+6823T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000306 | ||||||
chr14:90000447
|
C | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1541+6964C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000447 | ||||||
chr14:90000477
|
T | C | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+6994T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000477 | ||||||
chr14:90000530
|
A | G | 7 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0001g0120others(4): Show | 7 | HG02132.hp1 NA18951.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541+7047A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000530 | ||||||
chr14:90000534
|
G | A | 1 | a0001c0002t0004g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1541+7051G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000534 | ||||||
chr14:90000663
|
G | A | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+7180G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000663 | ||||||
chr14:90000708
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0202 | 3 | HG02280.hp2 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1541+7225G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000708 | ||||||
chr14:90000780
|
T | C | 83 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(80): Show | 88 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.1541+7297T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000780 | ||||||
chr14:90000803
|
T | C | 1 | a0001c0001t0002g0039 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1541+7320T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000803 | ||||||
chr14:90000837
|
A | T | 1 | a0001c0002t0004g0215 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1541+7354A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000837 | ||||||
chr14:90000909
|
G | A | 1 | a0005c0008t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1541+7426G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000909 | ||||||
chr14:90001094
|
T | C | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+7611T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001094 | ||||||
chr14:90001184
|
G | C | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+7701G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001184 | ||||||
chr14:90001248
|
C | T | 1 | a0001c0002t0013g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1541+7765C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001248 | ||||||
chr14:90001423
|
A | G | 3 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0243 | 3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1541+7940A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001423 | ||||||
chr14:90001648
|
A | C | 64 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(61): Show | 69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1541+8165A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001648 | ||||||
chr14:90001810
|
C | T | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+8327C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001810 | ||||||
chr14:90001829
|
T | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+8346T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001829 | ||||||
chr14:90001893
|
G | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+8410G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001893 | ||||||
chr14:90002143
|
C | T | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+8660C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002143 | ||||||
chr14:90002327
|
C | A | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+8844C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002327 | ||||||
chr14:90002354
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1541+8871A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002354 | ||||||
chr14:90002583
|
A | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+9100A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002583 | ||||||
chr14:90002706
|
C | CA | 7 | a0001c0001t0001g0110a0001c0001t0002g0037a0001c0002t0004g0221others(4): Show | 7 | HG01192.hp2 HG01981.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1541+9238dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90002706 | |||||
chr14:90002706
|
CA | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+9238delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90002706 | |||||
chr14:90002717
|
A | C | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1541+9234A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002717 | ||||||
chr14:90002734
|
T | A | 1 | a0002c0004t0009g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1541+9251T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002734 | ||||||
chr14:90002734
|
T | G | 20 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(17): Show | 23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1541+9251T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002734 | ||||||
chr14:90002819
|
G | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+9336G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002819 | ||||||
chr14:90002973
|
A | AT | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+9492dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90002973 | |||||
chr14:90002974
|
T | TG | 7 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+9491_1541+949 others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002974 | ||||||
chr14:90002999
|
A | G | 10 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(7): Show | 11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1541+9516A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002999 | ||||||
chr14:90003020
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1541+9537C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003020 | ||||||
chr14:90003126
|
T | C | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+9643T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003126 | ||||||
chr14:90003128
|
A | G | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+9645A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003128 | ||||||
chr14:90003157
|
C | T | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+9674C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003157 | ||||||
chr14:90003179
|
G | A | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+9696G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003179 | ||||||
chr14:90003246
|
A | G | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+9763A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003246 | ||||||
chr14:90003292
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1541+9809C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003292 | ||||||
chr14:90003349
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0011g0099 | 2 | NA18951.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1541+9866T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003349 | ||||||
chr14:90003482
|
G | A | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1541+9999G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003482 | ||||||
chr14:90003741
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+10258T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003741 | ||||||
chr14:90003889
|
T | C | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1541+10406T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003889 | ||||||
chr14:90003943
|
T | A | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+10460T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003943 | ||||||
chr14:90004019
|
G | A | 2 | a0001c0002t0004g0216a0001c0002t0004g0218 | 2 | HG01433.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1541+10536G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004019 | ||||||
chr14:90004027
|
A | G | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+10544A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004027 | ||||||
chr14:90004039
|
G | A | 1 | a0001c0002t0008g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1541+10556G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004039 | ||||||
chr14:90004046
|
T | G | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1541+10563T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004046 | ||||||
chr14:90004089
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+10606G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004089 | ||||||
chr14:90004113
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+10630G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004113 | ||||||
chr14:90004139
|
C | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+10656C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004139 | ||||||
chr14:90004269
|
T | C | 1 | a0001c0002t0004g0220 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1541+10786T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004269 | ||||||
chr14:90004282
|
T | C | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+10799T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004282 | ||||||
chr14:90004333
|
T | C | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+10850T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004333 | ||||||
chr14:90004433
|
G | A | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+10950G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004433 | ||||||
chr14:90004637
|
A | G | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+11154A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004637 | ||||||
chr14:90004685
|
T | TG | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+11203dupG | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90004685 | |||||
chr14:90004771
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0114 | 2 | HG00639.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.1541+11288T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004771 | ||||||
chr14:90004810
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1541+11327C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004810 | ||||||
chr14:90004929
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+11446T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004929 | ||||||
chr14:90004940
|
A | G | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+11457A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004940 | ||||||
chr14:90004974
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+11491A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004974 | ||||||
chr14:90005096
|
A | G | 2 | a0001c0002t0001g0206a0001c0002t0001g0207 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1541+11613A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005096 | ||||||
chr14:90005267
|
G | C | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+11784G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005267 | ||||||
chr14:90005414
|
A | T | 42 | a0001c0002t0014g0017a0002c0003t0003g0011a0002c0003t0003g0014others(39): Show | 47 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1541+11931A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005414 | ||||||
chr14:90005422
|
A | T | 5 | a0001c0001t0001g0127a0001c0001t0002g0035a0001c0001t0002g0043others(2): Show | 5 | HG02165.hp1 NA18942.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541+11939A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005422 | ||||||
chr14:90005435
|
A | G | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1541+11952A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005435 | ||||||
chr14:90006082
|
G | A | 14 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(11): Show | 14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1541+12599G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006082 | ||||||
chr14:90006092
|
C | T | 23 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(20): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1541+12609C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006092 | ||||||
chr14:90006243
|
C | T | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+12760C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006243 | ||||||
chr14:90006492
|
T | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-12824T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006492 | ||||||
chr14:90006754
|
G | C | 1 | a0002c0003t0003g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1542-12562G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006754 | ||||||
chr14:90006894
|
A | G | 3 | a0005c0008t0001g0146a0005c0008t0001g0147a0005c0008t0001g0148 | 3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1542-12422A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006894 | ||||||
chr14:90007244
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-12072C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007244 | ||||||
chr14:90007282
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1542-12034G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007282 | ||||||
chr14:90007326
|
T | C | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11990T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007326 | ||||||
chr14:90007354
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1542-11962C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007354 | ||||||
chr14:90007433
|
A | G | 4 | a0001c0001t0002g0001a0001c0001t0002g0036a0001c0001t0002g0042others(1): Show | 7 | NA18952.hp2 NA18970.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1542-11883A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007433 | ||||||
chr14:90007446
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1542-11870G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007446 | ||||||
chr14:90007526
|
T | G | 1 | a0001c0005t0016g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1542-11790T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007526 | ||||||
chr14:90007568
|
A | G | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1542-11748A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007568 | ||||||
chr14:90007574
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1542-11742G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007574 | ||||||
chr14:90007600
|
C | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11716C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007600 | ||||||
chr14:90007626
|
A | AT | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11679dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90007626 | |||||
chr14:90007626
|
A | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1542-11690A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007626 | ||||||
chr14:90007719
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1542-11597C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007719 | ||||||
chr14:90008035
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11281G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008035 | ||||||
chr14:90008052
|
C | G | 1 | a0001c0001t0002g0052 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1542-11264C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008052 | ||||||
chr14:90008096
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1542-11220G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008096 | ||||||
chr14:90008153
|
AT | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11161delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90008153 | |||||
chr14:90008219
|
A | C | 6 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542-11097A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008219 | ||||||
chr14:90008275
|
C | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11041C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008275 | ||||||
chr14:90008282
|
G | A | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1542-11034G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008282 | ||||||
chr14:90008348
|
C | CAT | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-10967_1542-10 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90008348 | |||||
chr14:90008420
|
C | A | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1542-10896C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008420 | ||||||
chr14:90008430
|
A | G | 2 | a0003c0006t0007g0090a0003c0006t0007g0091 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-10886A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008430 | ||||||
chr14:90008485
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-10831C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008485 | ||||||
chr14:90008491
|
G | A | 1 | a0001c0005t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1542-10825G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008491 | ||||||
chr14:90008514
|
A | G | 2 | a0001c0002t0004g0220a0001c0002t0004g0223 | 2 | HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1542-10802A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008514 | ||||||
chr14:90008580
|
G | T | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-10736G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008580 | ||||||
chr14:90009005
|
A | G | 21 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(18): Show | 24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-10311A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009005 | ||||||
chr14:90009375
|
A | G | 2 | a0001c0002t0004g0220a0001c0002t0004g0223 | 2 | HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1542-9941A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009375 | ||||||
chr14:90009411
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1542-9905A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009411 | ||||||
chr14:90009664
|
A | T | 13 | a0001c0001t0002g0007a0001c0001t0002g0034a0001c0001t0002g0049others(10): Show | 13 | HG01074.hp1 HG01123.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1542-9652A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009664 | ||||||
chr14:90009705
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1542-9611A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009705 | ||||||
chr14:90010014
|
C | T | 1 | a0003c0006t0007g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1542-9302C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010014 | ||||||
chr14:90010085
|
A | G | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1542-9231A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010085 | ||||||
chr14:90010263
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-9053A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010263 | ||||||
chr14:90010294
|
T | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-9022T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010294 | ||||||
chr14:90010537
|
T | C | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1542-8779T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010537 | ||||||
chr14:90010575
|
CGA | C | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1542-8731_1542-873 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90010575 | |||||
chr14:90010629
|
G | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-8687G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010629 | ||||||
chr14:90010661
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-8655C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010661 | ||||||
chr14:90010690
|
G | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-8626G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010690 | ||||||
chr14:90010905
|
A | G | 3 | a0005c0008t0001g0146a0005c0008t0001g0147a0005c0008t0001g0148 | 3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1542-8411A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010905 | ||||||
chr14:90011049
|
G | C | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-8267G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011049 | ||||||
chr14:90011154
|
C | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-8162C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011154 | ||||||
chr14:90011162
|
G | A | 3 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | HG00408.hp1 NA18747.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1542-8154G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011162 | ||||||
chr14:90011279
|
A | G | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1542-8037A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011279 | ||||||
chr14:90011300
|
A | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-8016A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011300 | ||||||
chr14:90011303
|
G | C | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-8013G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011303 | ||||||
chr14:90011542
|
G | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-7774G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011542 | ||||||
chr14:90011548
|
A | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-7768A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011548 | ||||||
chr14:90011663
|
T | C | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0071 | 3 | HG00738.hp2 HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1542-7653T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011663 | ||||||
chr14:90011744
|
C | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1542-7572C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011744 | ||||||
chr14:90011811
|
G | A | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-7505G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011811 | ||||||
chr14:90011817
|
G | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-7499G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011817 | ||||||
chr14:90011830
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1542-7486G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011830 | ||||||
chr14:90011855
|
A | G | 3 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0243 | 3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1542-7461A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011855 | ||||||
chr14:90011991
|
C | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-7325C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011991 | ||||||
chr14:90012056
|
G | A | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-7260G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012056 | ||||||
chr14:90012074
|
C | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-7242C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012074 | ||||||
chr14:90012429
|
C | T | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1542-6887C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012429 | ||||||
chr14:90012484
|
G | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-6832G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012484 | ||||||
chr14:90012543
|
A | T | 1 | a0001c0002t0004g0233 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1542-6773A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012543 | ||||||
chr14:90012689
|
G | C | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-6627G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012689 | ||||||
chr14:90012694
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1542-6622C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012694 | ||||||
chr14:90012810
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-6506A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012810 | ||||||
chr14:90012927
|
C | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-6389C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012927 | ||||||
chr14:90012951
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-6365G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012951 | ||||||
chr14:90013038
|
A | G | 1 | a0002c0004t0005g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1542-6278A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013038 | ||||||
chr14:90013068
|
A | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-6248A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013068 | ||||||
chr14:90013075
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1542-6241A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013075 | ||||||
chr14:90013180
|
G | A | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542-6136G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013180 | ||||||
chr14:90013190
|
A | C | 2 | a0001c0002t0001g0031a0001c0002t0003g0015 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1542-6126A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013190 | ||||||
chr14:90013289
|
T | C | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1542-6027T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013289 | ||||||
chr14:90013311
|
T | C | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-6005T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013311 | ||||||
chr14:90013477
|
C | A | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-5839C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013477 | ||||||
chr14:90013733
|
G | A | 3 | a0001c0002t0001g0031a0001c0002t0003g0015a0001c0002t0014g0017 | 3 | HG02559.hp2 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1542-5583G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013733 | ||||||
chr14:90013761
|
A | G | 29 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(26): Show | 33 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1542-5555A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013761 | ||||||
chr14:90013791
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1542-5525G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013791 | ||||||
chr14:90013912
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1542-5404T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013912 | ||||||
chr14:90013928
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | NA18942.hp2 NA18953.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1542-5388A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013928 | ||||||
chr14:90013960
|
T | A | 1 | a0001c0002t0001g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1542-5356T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013960 | ||||||
chr14:90013978
|
T | G | 15 | a0001c0002t0004g0222a0002c0004t0005g0008a0002c0004t0005g0074others(12): Show | 16 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1542-5338T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013978 | ||||||
chr14:90014032
|
C | T | 3 | a0001c0002t0004g0220a0001c0002t0004g0221a0001c0002t0004g0223 | 3 | HG02258.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1542-5284C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014032 | ||||||
chr14:90014119
|
C | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-5197C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014119 | ||||||
chr14:90014168
|
A | G | 1 | a0001c0002t0003g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1542-5148A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014168 | ||||||
chr14:90014186
|
A | G | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1542-5130A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014186 | ||||||
chr14:90014287
|
A | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-5029A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014287 | ||||||
chr14:90014351
|
A | G | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1542-4965A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014351 | ||||||
chr14:90014352
|
A | C | 1 | a0001c0001t0002g0049 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1542-4964A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014352 | ||||||
chr14:90014492
|
C | G | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-4824C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014492 | ||||||
chr14:90014751
|
C | G | 23 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(20): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1542-4565C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014751 | ||||||
chr14:90014753
|
T | A | 43 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(40): Show | 46 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1542-4563T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014753 | ||||||
chr14:90014795
|
G | A | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1542-4521G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014795 | ||||||
chr14:90014922
|
G | T | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1542-4394G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014922 | ||||||
chr14:90014963
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | NA18942.hp2 NA18953.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1542-4353A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014963 | ||||||
chr14:90014967
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1542-4349C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014967 | ||||||
chr14:90015029
|
A | G | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1542-4287A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015029 | ||||||
chr14:90015235
|
T | C | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1542-4081T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015235 | ||||||
chr14:90015444
|
C | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-3872C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015444 | ||||||
chr14:90015559
|
CA | C | 3 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0243 | 3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1542-3756delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015559 | ||||||
chr14:90015612
|
A | G | 243 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(240): Show | 260 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1542-3704A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015612 | ||||||
chr14:90015806
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1542-3510T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015806 | ||||||
chr14:90015915
|
G | C | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-3401G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015915 | ||||||
chr14:90015941
|
A | G | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1542-3375A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015941 | ||||||
chr14:90016046
|
C | CT | 18 | a0001c0001t0001g0169a0001c0001t0002g0063a0001c0002t0008g0209others(15): Show | 19 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1542-3258dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90016046 | |||||
chr14:90016193
|
T | C | 44 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(41): Show | 47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1542-3123T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016193 | ||||||
chr14:90016205
|
C | T | 51 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0169others(48): Show | 56 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.1542-3111C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016205 | ||||||
chr14:90016243
|
C | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-3073C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016243 | ||||||
chr14:90016311
|
G | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-3005G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016311 | ||||||
chr14:90016365
|
C | T | 1 | a0008c0009t0005g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1542-2951C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016365 | ||||||
chr14:90016457
|
T | C | 1 | a0001c0002t0010g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1542-2859T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016457 | ||||||
chr14:90016724
|
T | TAC | 21 | a0001c0001t0001g0129a0002c0003t0003g0011a0002c0003t0003g0014others(18): Show | 23 | HG01070.hp2 HG01361.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.1542-2578_1542-257 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90016724 | |||||
chr14:90016743
|
G | A | 65 | a0001c0002t0003g0205a0001c0002t0004g0215a0001c0002t0004g0216others(62): Show | 70 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.1542-2573G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016743 | ||||||
chr14:90016831
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00642.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1542-2485G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016831 | ||||||
chr14:90016919
|
C | G | 1 | a0001c0005t0016g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1542-2397C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016919 | ||||||
chr14:90016927
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1542-2389T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016927 | ||||||
chr14:90017090
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1542-2226A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017090 | ||||||
chr14:90017202
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-2114G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017202 | ||||||
chr14:90017321
|
TA | T | 64 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(61): Show | 69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1542-1993delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90017321 | |||||
chr14:90017328
|
G | A | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1542-1988G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017328 | ||||||
chr14:90017331
|
T | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152 | 3 | NA18947.hp2 NA18988.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1542-1985T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017331 | ||||||
chr14:90017365
|
T | G | 2 | a0001c0002t0008g0213a0001c0002t0008g0214 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1542-1951T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017365 | ||||||
chr14:90017370
|
A | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-1946A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017370 | ||||||
chr14:90017503
|
C | G | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-1813C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017503 | ||||||
chr14:90017527
|
A | T | 44 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(41): Show | 47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1542-1789A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017527 | ||||||
chr14:90017619
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1542-1697G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017619 | ||||||
chr14:90017904
|
T | G | 5 | a0002c0003t0003g0137a0002c0003t0003g0138a0002c0003t0003g0143others(2): Show | 5 | HG02602.hp2 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542-1412T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017904 | ||||||
chr14:90017973
|
T | C | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-1343T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017973 | ||||||
chr14:90017977
|
C | G | 1 | a0001c0005t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1542-1339C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017977 | ||||||
chr14:90018071
|
C | CT | 11 | a0001c0001t0001g0156a0001c0001t0002g0018a0001c0001t0002g0019others(8): Show | 11 | HG00738.hp2 HG01891.hp1 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.1542-1229dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90018071 | |||||
chr14:90018071
|
CT | C | 38 | a0001c0001t0001g0127a0001c0001t0001g0162a0001c0001t0002g0035others(35): Show | 40 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1542-1229delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90018071 | |||||
chr14:90018071
|
CTT | C | 46 | a0001c0002t0003g0205a0001c0002t0004g0215a0001c0002t0004g0216others(43): Show | 49 | HG00323.hp2 HG01070.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.1542-1230_1542-122 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90018071 | |||||
chr14:90018101
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1542-1215G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018101 | ||||||
chr14:90018151
|
A | C | 15 | a0001c0002t0001g0031a0001c0002t0003g0015a0001c0005t0001g0004others(12): Show | 16 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1542-1165A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018151 | ||||||
chr14:90018220
|
G | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-1096G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018220 | ||||||
chr14:90018333
|
A | G | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-983A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018333 | ||||||
chr14:90018341
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1542-975A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018341 | ||||||
chr14:90018392
|
G | C | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542-924G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018392 | ||||||
chr14:90018607
|
C | T | 1 | a0001c0002t0010g0235 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1542-709C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018607 | ||||||
chr14:90018692
|
G | A | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-624G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018692 | ||||||
chr14:90018700
|
C | T | 1 | a0001c0005t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1542-616C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018700 | ||||||
chr14:90018750
|
C | T | 2 | a0001c0005t0001g0023a0002c0004t0005g0082 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1542-566C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018750 | ||||||
chr14:90018795
|
C | T | 1 | a0002c0004t0005g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1542-521C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018795 | ||||||
chr14:90018929
|
A | G | 44 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(41): Show | 47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1542-387A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018929 | ||||||
chr14:90018959
|
T | TGCTAGTT others(7): Show |
14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-356_1542-343d others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90018959 | |||||
chr14:90018995
|
C | G | 7 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1542-321C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018995 | ||||||
chr14:90019033
|
GA | G | 6 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG00408.hp2 NA18947.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542-276delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90019033 | |||||
chr14:90019040
|
A | G | 6 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG00408.hp2 NA18947.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542-276A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90019040 | ||||||
chr14:90019290
|
C | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1542-26C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90019290 | ||||||
chr14:90019650
|
CTG | C | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1644+237_1644+238d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90019650 | |||||
chr14:90019719
|
C | T | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+301C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019719 | ||||||
chr14:90019882
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1644+464A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019882 | ||||||
chr14:90019883
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1644+465C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019883 | ||||||
chr14:90019912
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1644+494C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019912 | ||||||
chr14:90019965
|
C | T | 7 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644+547C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019965 | ||||||
chr14:90020029
|
G | A | 20 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(17): Show | 23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1644+611G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020029 | ||||||
chr14:90020188
|
T | G | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1644+770T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020188 | ||||||
chr14:90020285
|
T | C | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1644+867T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020285 | ||||||
chr14:90020285
|
TAC | T | 33 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(30): Show | 33 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.1644+877_1644+878d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020285 | |||||
chr14:90020309
|
G | T | 33 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(30): Show | 33 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.1644+891G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020309 | ||||||
chr14:90020354
|
T | TCCTC | 26 | a0001c0001t0001g0013a0001c0001t0001g0180a0001c0001t0015g0167others(23): Show | 28 | HG01891.hp1 HG01981.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1644+956_1644+959d others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020354 | |||||
chr14:90020354
|
T | TCCTCCCT others(13): Show |
39 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(36): Show | 41 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.1644+955_1644+956i others(22): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020354 | |||||
chr14:90020354
|
T | TCCTCCCT others(124): Show |
8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+955_1644+956i others(133): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020354 | |||||
chr14:90020364
|
C | CTCCCTCC others(5): Show |
14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+957_1644+958i others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020364 | |||||
chr14:90020374
|
C | CCCTT | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644+968_1644+971d others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020374 | |||||
chr14:90020374
|
C | T | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+956C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020374 | ||||||
chr14:90020423
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1644+1005C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020423 | ||||||
chr14:90020476
|
TTCCC | T | 48 | a0001c0001t0001g0093a0001c0001t0001g0127a0001c0001t0001g0172others(45): Show | 53 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.1644+1084_1644+108 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020476 | |||||
chr14:90020482
|
C | T | 53 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(50): Show | 56 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1644+1064C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020482 | ||||||
chr14:90020501
|
TCCCTTCC others(1): Show |
T | 10 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(7): Show | 11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1084_1644+109 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020501 | ||||||
chr14:90020509
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1644+1091G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020509 | ||||||
chr14:90020513
|
C | T | 10 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(7): Show | 11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1095C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020513 | ||||||
chr14:90020527
|
C | T | 10 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(7): Show | 11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1109C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020527 | ||||||
chr14:90020530
|
T | TTCCG | 3 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0243 | 3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1644+1115_1644+111 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020530 | |||||
chr14:90020534
|
T | C | 3 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0243 | 3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1644+1116T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020534 | ||||||
chr14:90020542
|
C | CTCCCTCC others(44): Show |
1 | a0001c0002t0006g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1644+1129_1644+113 others(55): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020542 | |||||
chr14:90020543
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1125T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020543 | ||||||
chr14:90020548
|
T | C | 33 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(30): Show | 33 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.1644+1130T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020548 | ||||||
chr14:90020548
|
T | TCCTTCCC others(6): Show |
7 | a0001c0001t0001g0107a0003c0006t0007g0002a0003c0006t0007g0087others(4): Show | 9 | HG00280.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1644+1136_1644+113 others(17): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020548 | |||||
chr14:90020552
|
T | C | 1 | a0001c0002t0006g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1644+1134T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020552 | ||||||
chr14:90020552
|
T | TCCCTCCC others(2): Show |
24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1644+1136_1644+113 others(13): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020552 | |||||
chr14:90020552
|
T | TCCCTCCC others(19): Show |
3 | a0001c0002t0006g0238a0001c0002t0006g0240a0001c0002t0006g0241 | 3 | HG02280.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1644+1136_1644+113 others(30): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020552 | |||||
chr14:90020555
|
T | C | 9 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(6): Show | 9 | HG01891.hp1 HG02886.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1644+1137T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020555 | ||||||
chr14:90020559
|
C | T | 35 | a0001c0001t0001g0107a0001c0002t0004g0215a0001c0002t0004g0216others(32): Show | 37 | HG00280.hp2 HG00323.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.1644+1141C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020559 | ||||||
chr14:90020559
|
CTCCCTCC others(50): Show |
C | 10 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(7): Show | 11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1155_1644+121 others(61): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020559 | |||||
chr14:90020563
|
C | CTCCCTTC others(6): Show |
14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1150_1644+115 others(17): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020563 | |||||
chr14:90020565
|
C | T | 7 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644+1147C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020565 | ||||||
chr14:90020569
|
C | T | 18 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(15): Show | 19 | HG01070.hp2 HG01891.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1644+1151C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020569 | ||||||
chr14:90020572
|
T | TCCCTCCC others(34): Show |
2 | a0001c0002t0006g0242a0001c0002t0006g0244 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1644+1154_1644+115 others(45): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020572 | ||||||
chr14:90020572
|
T | TTCCCTCC others(39): Show |
3 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0243 | 3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1644+1157_1644+115 others(50): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020572 | |||||
chr14:90020572
|
T | TTCCCTCC others(35): Show |
7 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644+1157_1644+115 others(46): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020572 | |||||
chr14:90020573
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1644+1155T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020573 | ||||||
chr14:90020576
|
T | C | 7 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644+1158T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020576 | ||||||
chr14:90020576
|
T | TTCCCTCC others(18): Show |
1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1644+1161_1644+116 others(29): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020576 | |||||
chr14:90020576
|
T | TTCCTTCC others(5): Show |
62 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0002g0001others(59): Show | 68 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.1644+1162_1644+117 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020576 | |||||
chr14:90020576
|
TTCCTTCC others(1): Show |
T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1644+1162_1644+116 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020576 | |||||
chr14:90020579
|
CTTCCCTC others(29): Show |
C | 10 | a0002c0003t0003g0014a0002c0003t0003g0145a0002c0003t0003g0194others(7): Show | 11 | HG01070.hp2 HG02559.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1162_1644+119 others(40): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020579 | ||||||
chr14:90020580
|
T | C | 5 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0242others(2): Show | 5 | HG01192.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1644+1162T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020580 | ||||||
chr14:90020580
|
T | TTCCCTCC others(9): Show |
22 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(19): Show | 22 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1644+1173_1644+117 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020580 | |||||
chr14:90020580
|
TTCCC | T | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0092others(36): Show | 41 | HG00323.hp1 HG00408.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1644+1184_1644+118 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020580 | |||||
chr14:90020582
|
C | CCCTCCCT others(4): Show |
1 | a0001c0001t0001g0169 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1644+1173_1644+117 others(15): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020582 | |||||
chr14:90020584
|
C | CTCCCTCC others(14): Show |
2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG02109.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1644+1179_1644+118 others(25): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020584 | |||||
chr14:90020584
|
C | CTCCCTCC others(1): Show |
14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1173_1644+117 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020584 | |||||
chr14:90020584
|
C | CTCCCTTC others(6): Show |
6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+1171_1644+117 others(17): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020584 | |||||
chr14:90020584
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1644+1166C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020584 | ||||||
chr14:90020592
|
C | T | 5 | a0001c0002t0006g0238a0001c0002t0006g0239a0001c0002t0006g0240others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1644+1174C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020592 | ||||||
chr14:90020616
|
G | C | 10 | a0002c0003t0003g0014a0002c0003t0003g0145a0002c0003t0003g0194others(7): Show | 11 | HG01070.hp2 HG02559.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1198G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020616 | ||||||
chr14:90020800
|
C | CTTTTTTT others(282): Show |
3 | a0001c0002t0004g0222a0001c0002t0004g0224a0001c0002t0004g0230 | 3 | HG02451.hp1 HG02896.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1644+1396_1644+139 others(293): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | |||||
chr14:90020800
|
C | CTTTTTTT others(282): Show |
1 | a0001c0002t0004g0233 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(293): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | |||||
chr14:90020800
|
C | CTTTTTTT others(283): Show |
2 | a0001c0002t0004g0216a0001c0002t0004g0218 | 2 | HG01433.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1644+1396_1644+139 others(294): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | |||||
chr14:90020800
|
C | CTTTTTTT others(282): Show |
1 | a0001c0002t0010g0234 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(293): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | |||||
chr14:90020800
|
C | CTTTTTTT others(283): Show |
13 | a0001c0002t0004g0217a0001c0002t0004g0219a0001c0002t0004g0220others(10): Show | 13 | HG00323.hp2 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1644+1396_1644+139 others(294): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | |||||
chr14:90020800
|
C | CTTTTTTT others(282): Show |
1 | a0001c0002t0004g0227 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(293): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | |||||
chr14:90020800
|
C | CTTTTTTT others(283): Show |
1 | a0001c0002t0004g0232 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(294): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | |||||
chr14:90020800
|
C | CTTTTTTT others(284): Show |
1 | a0001c0002t0004g0215 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(295): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | |||||
chr14:90020800
|
C | CTTTTTTT others(284): Show |
1 | a0001c0002t0010g0235 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(295): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | |||||
chr14:90020826
|
C | T | 1 | a0002c0004t0005g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1644+1408C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020826 | ||||||
chr14:90020834
|
C | T | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1644+1416C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020834 | ||||||
chr14:90020859
|
G | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1441G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020859 | ||||||
chr14:90020988
|
G | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1570G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020988 | ||||||
chr14:90021116
|
C | T | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644+1698C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021116 | ||||||
chr14:90021127
|
G | A | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+1709G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021127 | ||||||
chr14:90021177
|
C | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+1759C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021177 | ||||||
chr14:90021352
|
C | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+1934C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021352 | ||||||
chr14:90021628
|
T | G | 33 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(30): Show | 33 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.1644+2210T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021628 | ||||||
chr14:90021870
|
T | G | 2 | a0001c0002t0008g0213a0001c0002t0008g0214 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1644+2452T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021870 | ||||||
chr14:90021892
|
CAG | C | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644+2477_1644+247 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90021892 | |||||
chr14:90021995
|
T | C | 8 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0195others(5): Show | 9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+2577T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021995 | ||||||
chr14:90022082
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1644+2664C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022082 | ||||||
chr14:90022114
|
G | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+2696G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022114 | ||||||
chr14:90022179
|
TGA | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+2765_1644+276 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90022179 | |||||
chr14:90022248
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1644+2830C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022248 | ||||||
chr14:90022476
|
C | G | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1644+3058C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022476 | ||||||
chr14:90022568
|
C | T | 44 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(41): Show | 47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1644+3150C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022568 | ||||||
chr14:90022742
|
G | C | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+3324G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022742 | ||||||
chr14:90022770
|
C | T | 1 | a0004c0007t0002g0057 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1644+3352C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022770 | ||||||
chr14:90022804
|
A | T | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1644+3386A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022804 | ||||||
chr14:90022825
|
T | C | 1 | a0001c0002t0010g0234 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1644+3407T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022825 | ||||||
chr14:90022844
|
G | A | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1644+3426G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022844 | ||||||
chr14:90022913
|
C | T | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+3495C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022913 | ||||||
chr14:90022945
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+3527T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022945 | ||||||
chr14:90022954
|
G | A | 102 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(99): Show | 109 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(106): Show |
intron_variant | MODIFIER | c.1644+3536G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022954 | ||||||
chr14:90022986
|
A | G | 1 | a0001c0005t0016g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1644+3568A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022986 | ||||||
chr14:90023075
|
CTGG | C | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1644+3659_1644+366 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90023075 | |||||
chr14:90023200
|
GC | G | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1644+3783delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90023200 | ||||||
chr14:90023254
|
A | C | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+3836A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90023254 | ||||||
chr14:90023316
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1644+3898G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90023316 | ||||||
chr14:90023863
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1644+4445C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90023863 | ||||||
chr14:90024089
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1644+4671A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024089 | ||||||
chr14:90024095
|
C | G | 1 | a0001c0005t0001g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1644+4677C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024095 | ||||||
chr14:90024130
|
G | C | 25 | a0001c0001t0002g0054a0001c0002t0004g0215a0001c0002t0004g0216others(22): Show | 25 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1644+4712G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024130 | ||||||
chr14:90024204
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+4786C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024204 | ||||||
chr14:90024341
|
A | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+4923A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024341 | ||||||
chr14:90025004
|
C | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+5586C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025004 | ||||||
chr14:90025013
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1644+5595C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025013 | ||||||
chr14:90025131
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1644+5713A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025131 | ||||||
chr14:90025134
|
C | T | 2 | a0002c0003t0003g0194a0002c0003t0003g0200 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1644+5716C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025134 | ||||||
chr14:90025468
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1644+6050A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025468 | ||||||
chr14:90025583
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1644+6165G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025583 | ||||||
chr14:90025594
|
G | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+6176G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025594 | ||||||
chr14:90025789
|
A | C | 97 | a0001c0002t0001g0031a0001c0002t0001g0206a0001c0002t0001g0207others(94): Show | 103 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(100): Show |
intron_variant | MODIFIER | c.1644+6371A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025789 | ||||||
chr14:90025903
|
A | G | 1 | a0001c0002t0004g0222 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1644+6485A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025903 | ||||||
chr14:90026072
|
G | T | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1644+6654G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026072 | ||||||
chr14:90026377
|
C | T | 1 | a0001c0005t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1645-6729C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026377 | ||||||
chr14:90026567
|
C | T | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1645-6539C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026567 | ||||||
chr14:90026642
|
G | A | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1645-6464G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026642 | ||||||
chr14:90026698
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1645-6408G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026698 | ||||||
chr14:90026763
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-6343T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026763 | ||||||
chr14:90026769
|
T | G | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-6337T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026769 | ||||||
chr14:90026826
|
G | C | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-6280G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026826 | ||||||
chr14:90026908
|
T | A | 11 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(8): Show | 12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1645-6198T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026908 | ||||||
chr14:90026922
|
G | A | 5 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0139others(2): Show | 6 | HG02451.hp2 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1645-6184G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026922 | ||||||
chr14:90026956
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1645-6150A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026956 | ||||||
chr14:90027071
|
C | T | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1645-6035C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027071 | ||||||
chr14:90027192
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1645-5914C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027192 | ||||||
chr14:90027239
|
C | A | 1 | a0001c0001t0002g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1645-5867C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027239 | ||||||
chr14:90027264
|
C | T | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-5842C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027264 | ||||||
chr14:90027410
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1645-5696G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027410 | ||||||
chr14:90027431
|
A | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-5675A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027431 | ||||||
chr14:90027466
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1645-5640G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027466 | ||||||
chr14:90027479
|
A | C | 1 | a0001c0001t0001g0119 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1645-5627A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027479 | ||||||
chr14:90027507
|
G | A | 1 | a0001c0005t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1645-5599G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027507 | ||||||
chr14:90027705
|
G | C | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-5401G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027705 | ||||||
chr14:90027754
|
G | A | 2 | a0001c0002t0001g0031a0001c0002t0003g0015 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1645-5352G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027754 | ||||||
chr14:90028083
|
A | G | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1645-5023A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028083 | ||||||
chr14:90028301
|
C | A | 1 | a0001c0002t0003g0205 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1645-4805C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028301 | ||||||
chr14:90028439
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1645-4667C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028439 | ||||||
chr14:90028440
|
G | A | 1 | a0002c0003t0003g0198 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1645-4666G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028440 | ||||||
chr14:90028826
|
G | A | 2 | a0001c0001t0002g0048a0001c0001t0002g0062 | 2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1645-4280G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028826 | ||||||
chr14:90028965
|
A | G | 1 | a0001c0002t0001g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1645-4141A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028965 | ||||||
chr14:90029130
|
T | C | 2 | a0002c0003t0003g0194a0002c0003t0003g0200 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1645-3976T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029130 | ||||||
chr14:90029194
|
A | AT | 24 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0172others(21): Show | 24 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.1645-3891dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | |||||
chr14:90029194
|
A | ATT | 4 | a0001c0002t0004g0222a0001c0002t0004g0224a0002c0004t0005g0008others(1): Show | 5 | HG01109.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1645-3892_1645-389 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | |||||
chr14:90029194
|
A | ATTT | 10 | a0002c0004t0005g0074a0002c0004t0005g0075a0002c0004t0005g0077others(7): Show | 10 | HG00735.hp2 HG01081.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1645-3893_1645-389 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | |||||
chr14:90029194
|
AT | A | 21 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0001g0184others(18): Show | 22 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1645-3891delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | |||||
chr14:90029194
|
ATT | A | 22 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(19): Show | 23 | HG01070.hp2 HG01192.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1645-3892_1645-389 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | |||||
chr14:90029194
|
ATTT | A | 8 | a0002c0003t0003g0140a0002c0003t0012g0201a0003c0006t0007g0002others(5): Show | 10 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1645-3893_1645-389 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | |||||
chr14:90029197
|
T | A | 3 | a0001c0001t0001g0106a0005c0008t0001g0146a0005c0008t0001g0148 | 3 | HG02723.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1645-3909T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029197 | ||||||
chr14:90029198
|
T | A | 1 | a0005c0008t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1645-3908T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029198 | ||||||
chr14:90029199
|
T | A | 2 | a0002c0003t0003g0194a0002c0003t0003g0200 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1645-3907T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029199 | ||||||
chr14:90029200
|
T | A | 1 | a0005c0008t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1645-3906T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029200 | ||||||
chr14:90029229
|
G | A | 7 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1645-3877G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029229 | ||||||
chr14:90029336
|
T | C | 2 | a0001c0002t0001g0031a0001c0002t0003g0015 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1645-3770T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029336 | ||||||
chr14:90029345
|
G | A | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-3761G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029345 | ||||||
chr14:90029498
|
C | CT | 19 | a0001c0001t0001g0109a0001c0001t0001g0161a0001c0001t0001g0162others(16): Show | 20 | HG02071.hp1 HG02071.hp2 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.1645-3591dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | |||||
chr14:90029498
|
C | CTT | 26 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(23): Show | 26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1645-3592_1645-359 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | |||||
chr14:90029498
|
C | CTTT | 12 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(9): Show | 13 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1645-3593_1645-359 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | |||||
chr14:90029498
|
C | CTTTT | 8 | a0001c0002t0013g0210a0001c0002t0013g0211a0002c0004t0005g0076others(5): Show | 10 | HG01884.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1645-3594_1645-359 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | |||||
chr14:90029498
|
CT | C | 7 | a0002c0003t0003g0014a0002c0003t0003g0194a0002c0003t0003g0196others(4): Show | 8 | HG01070.hp2 HG03195.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1645-3591delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | |||||
chr14:90029561
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-3545C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029561 | ||||||
chr14:90029574
|
G | T | 1 | a0001c0001t0001g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1645-3532G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029574 | ||||||
chr14:90029728
|
A | G | 1 | a0001c0001t0001g0010 | 2 | NA18968.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1645-3378A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029728 | ||||||
chr14:90029775
|
A | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-3331A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029775 | ||||||
chr14:90029795
|
G | A | 2 | a0001c0002t0004g0220a0001c0002t0004g0223 | 2 | HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1645-3311G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029795 | ||||||
chr14:90030196
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1645-2910C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030196 | ||||||
chr14:90030204
|
C | T | 48 | a0001c0001t0001g0127a0001c0001t0001g0169a0001c0001t0001g0171others(45): Show | 53 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.1645-2902C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030204 | ||||||
chr14:90030266
|
C | T | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-2840C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030266 | ||||||
chr14:90030318
|
T | C | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1645-2788T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030318 | ||||||
chr14:90030403
|
C | T | 4 | a0001c0002t0006g0238a0001c0002t0006g0239a0001c0002t0006g0240others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1645-2703C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030403 | ||||||
chr14:90030739
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1645-2367G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030739 | ||||||
chr14:90030771
|
C | CT | 34 | a0001c0001t0001g0125a0001c0002t0001g0031a0001c0002t0003g0015others(31): Show | 37 | HG00741.hp2 HG01192.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1645-2323dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90030771 | |||||
chr14:90030771
|
C | CTT | 14 | a0001c0005t0001g0072a0002c0004t0005g0008a0002c0004t0005g0074others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-2324_1645-232 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90030771 | |||||
chr14:90030771
|
C | T | 1 | a0001c0002t0008g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1645-2335C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030771 | ||||||
chr14:90030931
|
A | AT | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-2164dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90030931 | |||||
chr14:90030938
|
T | A | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1645-2168T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030938 | ||||||
chr14:90031010
|
T | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-2096T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031010 | ||||||
chr14:90031024
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1645-2082C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031024 | ||||||
chr14:90031121
|
ATTATAC | A | 3 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0243 | 3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1645-1982_1645-197 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90031121 | |||||
chr14:90031214
|
T | C | 65 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(62): Show | 70 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.1645-1892T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031214 | ||||||
chr14:90031342
|
A | C | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1645-1764A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031342 | ||||||
chr14:90031438
|
C | T | 1 | a0003c0006t0007g0088 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1645-1668C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031438 | ||||||
chr14:90031495
|
A | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-1611A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031495 | ||||||
chr14:90031664
|
C | A | 83 | a0001c0002t0001g0031a0001c0002t0001g0206a0001c0002t0001g0207others(80): Show | 88 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.1645-1442C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031664 | ||||||
chr14:90031816
|
G | A | 44 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(41): Show | 47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1645-1290G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031816 | ||||||
chr14:90031900
|
G | T | 1 | a0002c0004t0005g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1645-1206G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031900 | ||||||
chr14:90032079
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-1027T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032079 | ||||||
chr14:90032183
|
G | C | 1 | a0001c0001t0002g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1645-923G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032183 | ||||||
chr14:90032217
|
A | G | 44 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(41): Show | 47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1645-889A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032217 | ||||||
chr14:90032248
|
C | T | 1 | a0001c0002t0014g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1645-858C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032248 | ||||||
chr14:90032249
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1645-857G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032249 | ||||||
chr14:90032259
|
T | A | 10 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(7): Show | 11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1645-847T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032259 | ||||||
chr14:90032329
|
G | T | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1645-777G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032329 | ||||||
chr14:90032361
|
G | T | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1645-745G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032361 | ||||||
chr14:90032379
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1645-727A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032379 | ||||||
chr14:90032456
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-650C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032456 | ||||||
chr14:90032457
|
A | G | 1 | a0006c0012t0012g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1645-649A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032457 | ||||||
chr14:90032545
|
C | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-561C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032545 | ||||||
chr14:90032590
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1645-516G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032590 | ||||||
chr14:90032763
|
A | G | 1 | a0001c0002t0003g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1645-343A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032763 | ||||||
chr14:90032938
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0002g0060 | 2 | HG00741.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1645-168C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032938 | ||||||
chr14:90032962
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1645-144C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032962 | ||||||
chr14:90032980
|
C | A | 3 | a0001c0002t0008g0209a0001c0002t0008g0213a0001c0002t0008g0214 | 3 | HG02965.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1645-126C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032980 | ||||||
chr14:90032980
|
C | G | 46 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(43): Show | 49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1645-126C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032980 | ||||||
chr14:90033006
|
A | T | 2 | a0001c0002t0013g0210a0001c0002t0013g0211 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1645-100A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90033006 | ||||||
chr14:90033045
|
G | GT | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-50dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90033045 | |||||
chr14:90033045
|
G | T | 2 | a0001c0002t0013g0210a0001c0002t0013g0211 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1645-61G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90033045 | ||||||
chr14:90033049
|
T | C | 1 | a0002c0003t0012g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1645-57T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90033049 | ||||||
chr14:90033081
|
A | T | 2 | a0001c0002t0004g0216a0001c0002t0004g0218 | 2 | HG01433.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1645-25A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90033081 | ||||||
chr14:90033451
|
T | C | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1753+237T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033451 | ||||||
chr14:90033507
|
G | A | 2 | a0001c0002t0013g0210a0001c0002t0013g0211 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1753+293G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033507 | ||||||
chr14:90033712
|
AT | A | 7 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753+500delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90033712 | |||||
chr14:90033739
|
C | T | 1 | a0001c0002t0001g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1753+525C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033739 | ||||||
chr14:90033768
|
G | A | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1753+554G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033768 | ||||||
chr14:90033826
|
G | A | 7 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753+612G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033826 | ||||||
chr14:90033946
|
A | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0125 | 3 | HG00741.hp2 HG02109.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1753+732A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033946 | ||||||
chr14:90033990
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1753+776C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033990 | ||||||
chr14:90033996
|
G | A | 1 | a0001c0005t0001g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1753+782G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033996 | ||||||
chr14:90034013
|
G | A | 26 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(23): Show | 26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1753+799G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034013 | ||||||
chr14:90034208
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+994C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034208 | ||||||
chr14:90034209
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+995T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034209 | ||||||
chr14:90034226
|
G | A | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1753+1012G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034226 | ||||||
chr14:90034307
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1753+1093C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034307 | ||||||
chr14:90034386
|
G | T | 1 | a0001c0005t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1753+1172G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034386 | ||||||
chr14:90034504
|
T | G | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1753+1290T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034504 | ||||||
chr14:90034813
|
C | G | 3 | a0001c0002t0008g0209a0001c0002t0008g0213a0001c0002t0008g0214 | 3 | HG02965.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1753+1599C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034813 | ||||||
chr14:90034835
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+1621T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034835 | ||||||
chr14:90034891
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1753+1677C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034891 | ||||||
chr14:90034931
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1753+1717T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034931 | ||||||
chr14:90035039
|
CTTCTCAG others(39): Show |
C | 3 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047 | 3 | NA18973.hp1 NA18983.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1753+1864_1753+190 others(50): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035039 | |||||
chr14:90035077
|
C | G | 2 | a0001c0002t0008g0213a0001c0002t0008g0214 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1753+1863C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035077 | ||||||
chr14:90035156
|
C | T | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1753+1942C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035156 | ||||||
chr14:90035215
|
C | T | 1 | a0001c0005t0016g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1753+2001C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035215 | ||||||
chr14:90035332
|
AAATCCCC others(10): Show |
A | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+2119_1753+213 others(21): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035332 | ||||||
chr14:90035333
|
A | G | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1753+2119A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035333 | ||||||
chr14:90035461
|
C | CA | 19 | a0001c0001t0001g0098a0001c0001t0001g0168a0001c0001t0001g0175others(16): Show | 20 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1753+2260dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035461 | |||||
chr14:90035590
|
A | G | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1753+2376A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035590 | ||||||
chr14:90035692
|
G | A | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+2478G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035692 | ||||||
chr14:90035733
|
C | CTTTTT | 23 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(20): Show | 23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1753+2530_1753+253 others(9): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035733 | |||||
chr14:90035733
|
C | CTTTTTTT | 5 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(2): Show | 7 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1753+2528_1753+253 others(11): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035733 | |||||
chr14:90035733
|
C | CTTTTTTT others(1): Show |
31 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(28): Show | 34 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1753+2527_1753+253 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035733 | |||||
chr14:90035983
|
C | T | 20 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(17): Show | 22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1753+2769C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035983 | ||||||
chr14:90036173
|
A | T | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1753+2959A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90036173 | ||||||
chr14:90036186
|
AC | A | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753+2973delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90036186 | ||||||
chr14:90036637
|
T | C | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+3423T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90036637 | ||||||
chr14:90036816
|
T | TA | 82 | a0001c0001t0001g0010a0001c0001t0001g0105a0001c0002t0001g0031others(79): Show | 87 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(84): Show |
intron_variant | MODIFIER | c.1753+3615dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90036816 | |||||
chr14:90036816
|
T | TAA | 12 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(9): Show | 14 | HG01192.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1753+3614_1753+361 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90036816 | |||||
chr14:90036972
|
C | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1753+3758C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90036972 | ||||||
chr14:90037008
|
C | T | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1753+3794C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037008 | ||||||
chr14:90037038
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+3824C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037038 | ||||||
chr14:90037040
|
G | A | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1753+3826G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037040 | ||||||
chr14:90037047
|
A | G | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1753+3833A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037047 | ||||||
chr14:90037065
|
G | A | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1753+3851G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037065 | ||||||
chr14:90037198
|
G | A | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1753+3984G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037198 | ||||||
chr14:90037316
|
G | C | 2 | a0001c0002t0008g0213a0001c0002t0008g0214 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1753+4102G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037316 | ||||||
chr14:90037377
|
ATAAAT | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0203 | 3 | HG01081.hp2 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1753+4165_1753+416 others(9): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90037377 | |||||
chr14:90037475
|
A | T | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753+4261A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037475 | ||||||
chr14:90037501
|
A | G | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+4287A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037501 | ||||||
chr14:90037529
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1753+4315G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037529 | ||||||
chr14:90037560
|
A | G | 4 | a0001c0005t0001g0004a0001c0005t0001g0028a0001c0005t0001g0030others(1): Show | 5 | HG02258.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1753+4346A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037560 | ||||||
chr14:90037581
|
G | A | 46 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(43): Show | 49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4367G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037581 | ||||||
chr14:90037582
|
C | T | 46 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(43): Show | 49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4368C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037582 | ||||||
chr14:90037585
|
A | G | 46 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(43): Show | 49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4371A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037585 | ||||||
chr14:90037650
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+4436T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037650 | ||||||
chr14:90037741
|
G | A | 46 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(43): Show | 49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4527G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037741 | ||||||
chr14:90038012
|
G | A | 46 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(43): Show | 49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4798G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038012 | ||||||
chr14:90038156
|
G | A | 46 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(43): Show | 49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1754-4914G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038156 | ||||||
chr14:90038186
|
T | A | 40 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(37): Show | 41 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.1754-4884T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038186 | ||||||
chr14:90038194
|
A | T | 2 | a0001c0002t0013g0210a0001c0002t0013g0211 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1754-4876A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038194 | ||||||
chr14:90038217
|
A | C | 2 | a0001c0002t0013g0210a0001c0002t0013g0211 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1754-4853A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038217 | ||||||
chr14:90038339
|
C | G | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1754-4731C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038339 | ||||||
chr14:90038363
|
A | C | 1 | a0001c0001t0011g0153 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1754-4707A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038363 | ||||||
chr14:90038402
|
T | A | 82 | a0001c0002t0001g0031a0001c0002t0003g0015a0001c0002t0003g0205others(79): Show | 87 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(84): Show |
intron_variant | MODIFIER | c.1754-4668T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038402 | ||||||
chr14:90038609
|
G | A | 4 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(1): Show | 4 | HG01891.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1754-4461G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038609 | ||||||
chr14:90038745
|
G | A | 2 | a0001c0002t0008g0213a0001c0002t0008g0214 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1754-4325G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038745 | ||||||
chr14:90038746
|
G | A | 2 | a0001c0002t0001g0031a0001c0002t0003g0015 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1754-4324G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038746 | ||||||
chr14:90038812
|
C | T | 46 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(43): Show | 49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1754-4258C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038812 | ||||||
chr14:90038904
|
G | GT | 23 | a0002c0003t0003g0011a0002c0003t0003g0014a0002c0003t0003g0016others(20): Show | 25 | HG01070.hp2 HG02145.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.1754-4154dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90038904 | |||||
chr14:90038904
|
G | GTT | 43 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(40): Show | 46 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1754-4155_1754-415 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90038904 | |||||
chr14:90038972
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1754-4098A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038972 | ||||||
chr14:90039016
|
T | G | 1 | a0001c0001t0002g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1754-4054T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039016 | ||||||
chr14:90039135
|
A | G | 24 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(21): Show | 24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1754-3935A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039135 | ||||||
chr14:90039206
|
A | C | 20 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0004g0217others(17): Show | 20 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1754-3864A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039206 | ||||||
chr14:90039316
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1754-3754T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039316 | ||||||
chr14:90039352
|
G | A | 2 | a0001c0002t0008g0213a0001c0002t0008g0214 | 2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1754-3718G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039352 | ||||||
chr14:90039495
|
C | T | 4 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(1): Show | 4 | HG01891.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1754-3575C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039495 | ||||||
chr14:90039512
|
A | G | 15 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0120others(12): Show | 15 | HG00323.hp1 HG00735.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1754-3558A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039512 | ||||||
chr14:90039549
|
G | A | 2 | a0001c0002t0001g0031a0001c0002t0003g0015 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1754-3521G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039549 | ||||||
chr14:90039586
|
C | T | 1 | a0002c0004t0005g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1754-3484C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039586 | ||||||
chr14:90039673
|
T | TTA | 3 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088 | 5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1754-3397_1754-339 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039673 | ||||||
chr14:90039673
|
T | TTAA | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1754-3397_1754-339 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039673 | ||||||
chr14:90039673
|
TA | T | 25 | a0001c0001t0001g0163a0001c0001t0002g0033a0001c0002t0004g0215others(22): Show | 25 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1754-3383delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90039673 | |||||
chr14:90039673
|
TAAA | T | 12 | a0002c0003t0003g0011a0002c0003t0003g0016a0002c0003t0003g0137others(9): Show | 13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1754-3385_1754-338 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90039673 | |||||
chr14:90039706
|
A | G | 1 | a0002c0003t0003g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1754-3364A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039706 | ||||||
chr14:90039933
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0097others(6): Show | 10 | HG00639.hp2 HG01109.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1754-3137A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039933 | ||||||
chr14:90039978
|
G | A | 1 | a0001c0002t0008g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1754-3092G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039978 | ||||||
chr14:90040744
|
A | G | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1754-2326A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90040744 | ||||||
chr14:90040919
|
A | G | 1 | a0002c0003t0003g0199 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1754-2151A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90040919 | ||||||
chr14:90040948
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG01109.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1754-2122A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90040948 | ||||||
chr14:90041166
|
C | T | 14 | a0002c0004t0005g0008a0002c0004t0005g0074a0002c0004t0005g0075others(11): Show | 15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1754-1904C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041166 | ||||||
chr14:90041246
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1754-1824A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041246 | ||||||
chr14:90041255
|
A | G | 3 | a0003c0006t0007g0089a0003c0006t0007g0090a0003c0006t0007g0091 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1754-1815A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041255 | ||||||
chr14:90041515
|
C | T | 1 | a0002c0003t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1754-1555C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041515 | ||||||
chr14:90041612
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1754-1458G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041612 | ||||||
chr14:90041661
|
G | A | 14 | a0001c0002t0001g0031a0001c0002t0003g0015a0001c0005t0001g0004others(11): Show | 15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1754-1409G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041661 | ||||||
chr14:90041731
|
T | C | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-1339T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041731 | ||||||
chr14:90041757
|
T | C | 48 | a0001c0001t0001g0127a0001c0001t0001g0169a0001c0001t0001g0171others(45): Show | 53 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.1754-1313T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041757 | ||||||
chr14:90041776
|
T | C | 1 | a0001c0002t0004g0228 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1754-1294T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041776 | ||||||
chr14:90041899
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1754-1171C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041899 | ||||||
chr14:90041942
|
A | G | 6 | a0003c0006t0007g0002a0003c0006t0007g0087a0003c0006t0007g0088others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1754-1128A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041942 | ||||||
chr14:90041980
|
A | T | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-1090A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041980 | ||||||
chr14:90042103
|
G | A | 1 | a0001c0002t0004g0215 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1754-967G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042103 | ||||||
chr14:90042410
|
T | A | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-660T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042410 | ||||||
chr14:90042422
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1754-648T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042422 | ||||||
chr14:90042466
|
A | G | 1 | a0001c0001t0002g0039 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1754-604A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042466 | ||||||
chr14:90042624
|
G | A | 9 | a0001c0002t0006g0236a0001c0002t0006g0237a0001c0002t0006g0238others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-446G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042624 | ||||||
chr14:90042734
|
G | A | 3 | a0001c0002t0008g0209a0001c0002t0008g0213a0001c0002t0008g0214 | 3 | HG02965.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1754-336G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042734 | ||||||
chr14:90042886
|
G | A | 1 | a0001c0001t0002g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1754-184G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042886 | ||||||
chr14:90042921
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1754-149C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042921 | ||||||
chr14:90042966
|
C | T | 1 | a0001c0001t0002g0006 | 2 | NA18944.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1754-104C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042966 | ||||||
chr14:90042988
|
A | G | 2 | a0001c0002t0004g0222a0001c0002t0004g0224 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1754-82A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042988 |