geneid | 7249 |
---|---|
ensemblid | ENSG00000103197.19 |
hgncid | 12363 |
symbol | TSC2 |
name | TSC complex subunit 2 |
refseq_nuc | NM_000548.5 |
refseq_prot | NP_000539.2 |
ensembl_nuc | ENST00000219476.9 |
ensembl_prot | ENSP00000219476.3 |
mane_status | MANE Select |
chr | chr16 |
start | 2047985 |
end | 2089491 |
strand | + |
ver | v1.2 |
region | chr16:2047985-2089491 |
region5000 | chr16:2042985-2094491 |
regionname0 | TSC2_chr16_2047985_2089491 |
regionname5000 | TSC2_chr16_2042985_2094491 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1807 | 275 | 78 | 71 | 72 | 14 | 38 | 48 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0002 | 0/0 | 1807 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0003 | 0/0 | 1807 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0004 | 0/0 | 1807 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0005 | 0/0 | 1807 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0006 | 0/0 | 1807 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0007 | 0/0 | 1807 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0008 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0009 | 0/0 | 1807 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0010 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0011 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0012 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0013 | 0/0 | 1715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0014 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0015 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0016 | 0/0 | 1801 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0017 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0018 | 0/0 | 1817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0019 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0020 | 0/0 | 1807 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0021 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0022 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0023 | 0/0 | 1807 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0024 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 5424 | 179 | 17 | 53 | 68 | 8 | 32 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0002 | 0/1 | 5424 | 31 | 22 | 7 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0003 | 0/0 | 5424 | 13 | 11 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0004 | 0/0 | 5424 | 8 | 8 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0005 | 0/0 | 5424 | 8 | 0 | 0 | 8 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0006 | 0/0 | 5424 | 7 | 6 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0007 | 0/0 | 5424 | 6 | 6 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0008 | 0/0 | 5424 | 4 | 0 | 2 | 0 | 1 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0009 | 0/0 | 5424 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0010 | 0/0 | 5424 | 3 | 0 | 0 | 0 | 2 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0011 | 0/0 | 5424 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0012 | 0/0 | 5424 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0013 | 0/0 | 5424 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0014 | 0/0 | 5424 | 2 | 0 | 1 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0015 | 0/0 | 5424 | 2 | 1 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0016 | 0/0 | 5424 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0017 | 0/0 | 5424 | 2 | 0 | 0 | 0 | 0 | 2 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0018 | 0/0 | 5424 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0019 | 0/0 | 5424 | 2 | 0 | 1 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0020 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0021 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0022 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0023 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0024 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0025 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0026 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0027 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0028 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0029 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0030 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0031 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0032 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0033 | 0/0 | 5454 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0034 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0035 | 0/0 | 5458 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0036 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0037 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0038 | 0/0 | 5406 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0039 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0040 | 0/0 | 5458 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0041 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0042 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0043 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0044 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0045 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0046 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0047 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0048 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0049 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0050 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0051 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0052 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0053 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0054 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
c0055 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 992 | 162 | 20 | 39 | 63 | 12 | 27 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0002 | 0/1 | 998 | 29 | 20 | 7 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0003 | 0/0 | 994 | 27 | 0 | 13 | 13 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0004 | 0/0 | 988 | 12 | 10 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0005 | 0/0 | 1000 | 11 | 9 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0006 | 0/0 | 998 | 9 | 9 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0007 | 0/0 | 992 | 8 | 0 | 3 | 0 | 1 | 4 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0008 | 0/0 | 986 | 7 | 0 | 1 | 0 | 0 | 6 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0009 | 0/0 | 986 | 6 | 0 | 3 | 0 | 1 | 2 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0010 | 0/0 | 992 | 5 | 4 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0011 | 0/0 | 994 | 4 | 3 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0012 | 0/0 | 992 | 4 | 4 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0013 | 0/0 | 996 | 3 | 0 | 0 | 3 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0014 | 0/0 | 990 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0015 | 0/0 | 994 | 3 | 0 | 0 | 2 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0016 | 0/0 | 990 | 2 | 1 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0017 | 0/0 | 994 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0018 | 0/0 | 1000 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0019 | 0/0 | 980 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0020 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0021 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0022 | 0/0 | 992 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0023 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0024 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0025 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0026 | 0/0 | 990 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0027 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0028 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0029 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0030 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0031 | 0/0 | 1006 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0032 | 0/0 | 1016 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0033 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0034 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0035 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0036 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0037 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0038 | 0/0 | 992 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
t0039 | 0/0 | 990 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0003 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0007 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5424 | 179 | 17 | 53 | 68 | 8 | 32 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0002 | 0/1 | 5424 | 31 | 22 | 7 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0003 | 0/0 | 5424 | 13 | 11 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0004 | 0/0 | 5424 | 8 | 8 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0007 | 0/0 | 5424 | 6 | 6 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0008 | 0/0 | 5424 | 4 | 0 | 2 | 0 | 1 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0009 | 0/0 | 5424 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0012 | 0/0 | 5424 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0014 | 0/0 | 5424 | 2 | 0 | 1 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0015 | 0/0 | 5424 | 2 | 1 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0016 | 0/0 | 5424 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0017 | 0/0 | 5424 | 2 | 0 | 0 | 0 | 0 | 2 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0019 | 0/0 | 5424 | 2 | 0 | 1 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0020 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0021 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0022 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0024 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0032 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0034 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0036 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0037 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0039 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0041 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0046 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0047 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0048 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0049 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0050 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0051 | 0/0 | 5424 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0052 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0053 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0002c0005 | 0/0 | 5424 | 8 | 0 | 0 | 8 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0003c0006 | 0/0 | 5424 | 7 | 6 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0004c0011 | 0/0 | 5424 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0004c0023 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0005c0010 | 0/0 | 5424 | 3 | 0 | 0 | 0 | 2 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0006c0013 | 0/0 | 5424 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0007c0018 | 0/0 | 5424 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0008c0028 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0009c0044 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0010c0030 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0011c0042 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0012c0045 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0013c0035 | 0/0 | 5458 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0014c0029 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0015c0040 | 0/0 | 5458 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0016c0038 | 0/0 | 5406 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0017c0043 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0018c0033 | 0/0 | 5454 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0019c0031 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0020c0027 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0021c0026 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0022c0025 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0023c0054 | 0/0 | 5424 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0024c0055 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6415 | 126 | 13 | 37 | 48 | 7 | 20 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0002 | 0/0 | 6421 | 2 | 0 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0003 | 0/0 | 6417 | 23 | 0 | 11 | 11 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0007 | 0/0 | 6415 | 4 | 0 | 0 | 0 | 0 | 4 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0008 | 0/0 | 6409 | 6 | 0 | 1 | 0 | 0 | 5 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0010 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0013 | 0/0 | 6419 | 3 | 0 | 0 | 3 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0015 | 0/0 | 6417 | 2 | 0 | 0 | 1 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0016 | 0/0 | 6413 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0017 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0019 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0020 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0021 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0022 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0023 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0024 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0026 | 0/0 | 6413 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0028 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0034 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0001t0038 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0002t0002 | 0/1 | 6421 | 17 | 13 | 3 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0002t0005 | 0/0 | 6423 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0002t0006 | 0/0 | 6421 | 7 | 7 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0002t0007 | 0/0 | 6415 | 4 | 0 | 3 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0002t0016 | 0/0 | 6413 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0002t0018 | 0/0 | 6423 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0003t0004 | 0/0 | 6411 | 12 | 10 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0003t0010 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0004t0005 | 0/0 | 6423 | 8 | 8 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0007t0002 | 0/0 | 6421 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0007t0012 | 0/0 | 6415 | 4 | 4 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0008t0009 | 0/0 | 6409 | 4 | 0 | 2 | 0 | 1 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0009t0014 | 0/0 | 6413 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0012t0001 | 0/0 | 6415 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0014t0009 | 0/0 | 6409 | 2 | 0 | 1 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0015t0005 | 0/0 | 6423 | 2 | 1 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0016t0001 | 0/0 | 6415 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0017t0001 | 0/0 | 6415 | 2 | 0 | 0 | 0 | 0 | 2 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0019t0002 | 0/0 | 6421 | 2 | 0 | 1 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0020t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0021t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0022t0001 | 0/0 | 6415 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0024t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0032t0001 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0034t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0036t0006 | 0/0 | 6421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0037t0027 | 0/0 | 6413 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0039t0039 | 0/0 | 6413 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0041t0001 | 0/0 | 6415 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0046t0006 | 0/0 | 6421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0047t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0048t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0049t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0050t0035 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0051t0003 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0052t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0001c0053t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0002c0005t0001 | 0/0 | 6415 | 7 | 0 | 0 | 7 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0002c0005t0003 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0003c0006t0002 | 0/0 | 6421 | 5 | 4 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0003c0006t0036 | 0/0 | 6425 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0003c0006t0037 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0004c0011t0011 | 0/0 | 6417 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0004c0011t0029 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0004c0023t0011 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0005c0010t0001 | 0/0 | 6415 | 3 | 0 | 0 | 0 | 2 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0006c0013t0010 | 0/0 | 6415 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0007c0018t0030 | 0/0 | 6431 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0007c0018t0032 | 0/0 | 6439 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0008c0028t0010 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0009c0044t0008 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0010c0030t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0011c0042t0002 | 0/0 | 6421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0012c0045t0025 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0013c0035t0011 | 0/0 | 6451 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0014c0029t0031 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0015c0040t0033 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0016c0038t0003 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0017c0043t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0018c0033t0001 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0019c0031t0015 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0020c0027t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0021c0026t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0022c0025t0001 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0023c0054t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
a0024c0055t0003 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | copy fasta | chr16 | 2042985 | 2094491 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0007 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0007g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0010g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0013g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0013g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0013g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0015g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0015g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0016g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0017g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0019g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0020g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0021g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0022g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0023g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0024g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0026g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0028g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0034g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0038g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0007g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0007g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0007g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0016g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0018g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0007t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0007t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0007t0012g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0007t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0007t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0008t0009g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0008t0009g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0008t0009g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0008t0009g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0009t0014g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0009t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0012t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0012t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0012t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0014t0009g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0014t0009g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0015t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0015t0005g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0016t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0016t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0017t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0017t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0019t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0019t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0020t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0021t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0022t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0024t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0032t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0034t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0036t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0037t0027g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0039t0039g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0041t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0046t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0047t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0048t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0049t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0050t0035g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0051t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0052t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0053t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0036g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0037g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0004c0011t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0004c0011t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0004c0011t0029g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0004c0023t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0005c0010t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0005c0010t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0005c0010t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0006c0013t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0006c0013t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0007c0018t0030g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0007c0018t0032g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0008c0028t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0009c0044t0008g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0010c0030t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0011c0042t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0012c0045t0025g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0013c0035t0011g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0014c0029t0031g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0015c0040t0033g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0016c0038t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0017c0043t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0018c0033t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0019c0031t0015g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0020c0027t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0021c0026t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0022c0025t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0023c0054t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0024c0055t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0038 | g0177 | EUR | GBR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00099 | hp2 | a0001 | c0052 | t0001 | g0015 | EUR | GBR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00140 | hp2 | a0001 | c0049 | t0001 | g0031 | EUR | GBR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00280 | hp1 | a0001 | c0019 | t0002 | g0037 | EUR | FIN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | FIN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00408 | hp2 | a0021 | c0026 | t0001 | g0173 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00438 | hp1 | a0024 | c0055 | t0003 | g0187 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00544 | hp1 | a0001 | c0001 | t0013 | g0236 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00558 | hp1 | a0001 | c0001 | t0017 | g0176 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00609 | hp2 | a0001 | c0001 | t0022 | g0165 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00621 | hp1 | a0019 | c0031 | t0015 | g0004 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0288 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00639 | hp2 | a0001 | c0008 | t0009 | g0030 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00733 | hp2 | a0016 | c0038 | t0003 | g0100 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00741 | hp1 | a0001 | c0001 | t0008 | g0097 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00741 | hp2 | a0001 | c0014 | t0009 | g0049 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01069 | hp2 | a0001 | c0003 | t0004 | g0126 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01070 | hp2 | a0013 | c0035 | t0011 | g0024 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01071 | hp1 | a0001 | c0003 | t0004 | g0127 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01081 | hp1 | a0001 | c0002 | t0005 | g0050 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01106 | hp1 | a0001 | c0039 | t0039 | g0185 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01109 | hp1 | a0001 | c0041 | t0001 | g0229 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01109 | hp2 | a0001 | c0015 | t0005 | g0278 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01192 | hp2 | a0001 | c0022 | t0001 | g0109 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01243 | hp2 | a0003 | c0006 | t0002 | g0285 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01257 | hp2 | a0001 | c0002 | t0007 | g0159 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01258 | hp2 | a0001 | c0002 | t0007 | g0163 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01261 | hp1 | a0001 | c0002 | t0007 | g0228 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01346 | hp1 | a0001 | c0008 | t0009 | g0064 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0263 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01496 | hp2 | a0001 | c0019 | t0002 | g0052 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01516 | hp1 | a0005 | c0010 | t0001 | g0244 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01517 | hp1 | a0005 | c0010 | t0001 | g0243 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01884 | hp2 | a0001 | c0004 | t0005 | g0012 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01891 | hp1 | a0001 | c0007 | t0012 | g0005 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01891 | hp2 | a0015 | c0040 | t0033 | g0267 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01928 | hp1 | a0001 | c0051 | t0003 | g0233 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01928 | hp2 | a0001 | c0001 | t0026 | g0011 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02015 | hp1 | a0001 | c0047 | t0001 | g0079 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02015 | hp2 | a0002 | c0005 | t0001 | g0070 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02040 | hp2 | a0001 | c0001 | t0013 | g0220 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02080 | hp2 | a0017 | c0043 | t0001 | g0215 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0279 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02145 | hp2 | a0001 | c0016 | t0001 | g0275 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02155 | hp1 | a0001 | c0001 | t0013 | g0260 | EAS | CDX | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02155 | hp2 | a0001 | c0001 | t0020 | g0170 | EAS | CDX | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02257 | hp1 | a0007 | c0018 | t0030 | g0122 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0289 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02258 | hp2 | a0004 | c0023 | t0011 | g0164 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02280 | hp1 | a0003 | c0006 | t0036 | g0013 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02280 | hp2 | a0001 | c0002 | t0006 | g0017 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02300 | hp2 | a0001 | c0001 | t0016 | g0295 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02451 | hp1 | a0001 | c0001 | t0024 | g0016 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02451 | hp2 | a0001 | c0004 | t0005 | g0140 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02572 | hp1 | a0003 | c0006 | t0002 | g0284 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02602 | hp1 | a0005 | c0010 | t0001 | g0245 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02615 | hp1 | a0001 | c0016 | t0001 | g0096 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02615 | hp2 | a0011 | c0042 | t0002 | g0133 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02622 | hp1 | a0001 | c0001 | t0034 | g0160 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02622 | hp2 | a0001 | c0003 | t0004 | g0142 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02630 | hp1 | a0001 | c0004 | t0005 | g0286 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02630 | hp2 | a0001 | c0002 | t0006 | g0040 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02647 | hp2 | a0001 | c0012 | t0001 | g0131 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02717 | hp2 | a0001 | c0003 | t0004 | g0146 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0035 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02723 | hp2 | a0001 | c0009 | t0014 | g0141 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02735 | hp2 | a0001 | c0014 | t0009 | g0194 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02809 | hp2 | a0004 | c0011 | t0029 | g0025 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02818 | hp1 | a0001 | c0003 | t0004 | g0148 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02818 | hp2 | a0001 | c0004 | t0005 | g0281 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02886 | hp1 | a0001 | c0012 | t0001 | g0080 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0282 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02895 | hp1 | a0001 | c0002 | t0006 | g0044 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02896 | hp1 | a0001 | c0003 | t0004 | g0150 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02896 | hp2 | a0001 | c0007 | t0012 | g0022 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02897 | hp1 | a0001 | c0003 | t0004 | g0149 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0060 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02922 | hp1 | a0001 | c0007 | t0002 | g0041 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02922 | hp2 | a0001 | c0004 | t0005 | g0014 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02965 | hp2 | a0006 | c0013 | t0010 | g0139 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02970 | hp1 | a0001 | c0009 | t0014 | g0008 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02970 | hp2 | a0003 | c0006 | t0002 | g0287 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03041 | hp1 | a0001 | c0004 | t0005 | g0283 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03041 | hp2 | a0001 | c0050 | t0035 | g0298 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03098 | hp2 | a0014 | c0029 | t0031 | g0034 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03130 | hp1 | a0007 | c0018 | t0032 | g0123 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03130 | hp2 | a0003 | c0006 | t0002 | g0291 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03139 | hp2 | a0006 | c0013 | t0010 | g0137 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03195 | hp1 | a0001 | c0002 | t0006 | g0021 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0290 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03209 | hp2 | a0012 | c0045 | t0025 | g0299 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03225 | hp1 | a0001 | c0007 | t0002 | g0042 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03225 | hp2 | a0004 | c0011 | t0011 | g0026 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03239 | hp1 | a0009 | c0044 | t0008 | g0098 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03239 | hp2 | a0001 | c0001 | t0008 | g0124 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03453 | hp1 | a0001 | c0007 | t0012 | g0005 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03453 | hp2 | a0008 | c0028 | t0010 | g0138 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03486 | hp1 | a0001 | c0009 | t0014 | g0008 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03486 | hp2 | a0003 | c0006 | t0002 | g0013 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03491 | hp1 | a0001 | c0017 | t0001 | g0293 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03491 | hp2 | a0001 | c0001 | t0008 | g0155 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03492 | hp1 | a0001 | c0017 | t0001 | g0208 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0257 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0276 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03516 | hp2 | a0001 | c0002 | t0016 | g0128 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03540 | hp1 | a0001 | c0007 | t0012 | g0023 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03540 | hp2 | a0001 | c0003 | t0004 | g0147 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03579 | hp1 | a0003 | c0006 | t0037 | g0274 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03579 | hp2 | a0001 | c0003 | t0004 | g0144 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03654 | hp2 | a0023 | c0054 | t0001 | g0113 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03669 | hp2 | a0001 | c0001 | t0019 | g0241 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0253 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03704 | hp1 | a0001 | c0001 | t0015 | g0239 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03704 | hp2 | a0001 | c0001 | t0008 | g0072 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03710 | hp1 | a0001 | c0008 | t0009 | g0033 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0222 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03942 | hp1 | a0020 | c0027 | t0001 | g0019 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03942 | hp2 | a0001 | c0001 | t0008 | g0264 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04115 | hp2 | a0001 | c0048 | t0001 | g0028 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04199 | hp2 | a0001 | c0001 | t0007 | g0251 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04204 | hp1 | a0001 | c0053 | t0001 | g0169 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04228 | hp1 | a0001 | c0001 | t0007 | g0226 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18522 | hp2 | a0001 | c0003 | t0004 | g0297 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18612 | hp1 | a0002 | c0005 | t0001 | g0088 | EAS | CHB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18906 | hp1 | a0001 | c0004 | t0005 | g0014 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18906 | hp2 | a0001 | c0003 | t0004 | g0151 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18950 | hp2 | a0001 | c0001 | t0010 | g0156 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18960 | hp1 | a0002 | c0005 | t0001 | g0111 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18961 | hp2 | a0002 | c0005 | t0003 | g0104 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18966 | hp1 | a0002 | c0005 | t0001 | g0078 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18974 | hp2 | a0002 | c0005 | t0001 | g0089 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18975 | hp2 | a0002 | c0005 | t0001 | g0087 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18980 | hp1 | a0001 | c0021 | t0001 | g0201 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18980 | hp2 | a0002 | c0005 | t0001 | g0254 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18997 | hp1 | a0018 | c0033 | t0001 | g0110 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18997 | hp2 | a0001 | c0024 | t0001 | g0192 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19011 | hp2 | a0010 | c0030 | t0001 | g0074 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19030 | hp1 | a0001 | c0002 | t0006 | g0048 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19030 | hp2 | a0001 | c0037 | t0027 | g0059 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19043 | hp1 | a0001 | c0032 | t0001 | g0121 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19043 | hp2 | a0001 | c0046 | t0006 | g0043 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19068 | hp1 | a0001 | c0034 | t0001 | g0003 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19068 | hp2 | a0001 | c0001 | t0021 | g0083 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19088 | hp2 | a0001 | c0001 | t0015 | g0118 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19240 | hp1 | a0001 | c0015 | t0005 | g0277 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19240 | hp2 | a0001 | c0001 | t0023 | g0081 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20129 | hp1 | a0001 | c0003 | t0010 | g0145 | AFR | ASW | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20129 | hp2 | a0001 | c0004 | t0005 | g0012 | AFR | ASW | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | TSI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20752 | hp2 | a0001 | c0008 | t0009 | g0029 | EUR | TSI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20805 | hp1 | a0001 | c0002 | t0007 | g0227 | EUR | TSI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20805 | hp2 | a0001 | c0020 | t0001 | g0247 | EUR | TSI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0280 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02109 | hp2 | a0001 | c0003 | t0004 | g0296 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02486 | hp1 | a0001 | c0012 | t0001 | g0073 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02486 | hp2 | a0004 | c0011 | t0011 | g0027 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02559 | hp1 | a0001 | c0002 | t0006 | g0045 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03471 | hp1 | a0001 | c0036 | t0006 | g0046 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG06807 | hp2 | a0022 | c0025 | t0001 | g0129 | AFR | USA | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20300 | hp1 | a0001 | c0001 | t0028 | g0055 | AFR | USA | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | USA | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA21309 | hp1 | a0001 | c0002 | t0018 | g0053 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0039 | REF | REF | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:2048740
|
C | T | 1 | a0024 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.125C>T | p.Ala42Val | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/42 | 235/6415 | 125/5424 | 42/1807 | chr16 | 2048740 | ||
chr16:2053342
|
C | T | 1 | a0023 | 1 | HG03654.hp2 | missense_variant&splice_region_variant | MODERATE | c.226C>T | p.His76Tyr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 4/42 | 336/6415 | 226/5424 | 76/1807 | chr16 | 2053342 | ||
chr16:2058754
|
A | G | 1 | a0002 | 8 | HG02015.hp2 NA18612.hp1 NA18960.hp1 others(5): Show |
missense_variant | MODERATE | c.856A>G | p.Met286Val | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/42 | 966/6415 | 856/5424 | 286/1807 | chr16 | 2058754 | ||
chr16:2060794
|
G | A | 1 | a0005 | 3 | HG01516.hp1 HG01517.hp1 HG02602.hp1 |
missense_variant | MODERATE | c.1100G>A | p.Arg367Gln | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/42 | 1210/6415 | 1100/5424 | 367/1807 | chr16 | 2060794 | ||
chr16:2071609
|
G | T | 1 | a0023 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1939G>T | p.Asp647Tyr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 18/42 | 2049/6415 | 1939/5424 | 647/1807 | chr16 | 2071609 | ||
chr16:2071616
|
T | C | 1 | a0022 | 1 | HG06807.hp2 | missense_variant&splice_region_variant | MODERATE | c.1946T>C | p.Met649Thr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 18/42 | 2056/6415 | 1946/5424 | 649/1807 | chr16 | 2071616 | ||
chr16:2071869
|
G | A | 1 | a0021 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.2032G>A | p.Ala678Thr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 19/42 | 2142/6415 | 2032/5424 | 678/1807 | chr16 | 2071869 | ||
chr16:2072885
|
G | A | 1 | a0020 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.2257G>A | p.Ala753Thr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/42 | 2367/6415 | 2257/5424 | 753/1807 | chr16 | 2072885 | ||
chr16:2072924
|
G | A | 2 | a0006a0008 | 3 | HG02965.hp2 HG03139.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.2296G>A | p.Val766Met | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/42 | 2406/6415 | 2296/5424 | 766/1807 | chr16 | 2072924 | ||
chr16:2072976
|
C | G | 1 | a0009 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.2348C>G | p.Thr783Ser | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/42 | 2458/6415 | 2348/5424 | 783/1807 | chr16 | 2072976 | ||
chr16:2075846
|
T | C | 1 | a0010 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.2593T>C | p.Tyr865His | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/42 | 2703/6415 | 2593/5424 | 865/1807 | chr16 | 2075846 | ||
chr16:2077630
|
T | G | 1 | a0019 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.2870T>G | p.Leu957Trp | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/42 | 2980/6415 | 2870/5424 | 957/1807 | chr16 | 2077630 | ||
chr16:2080189
|
C | T | 1 | a0003 | 7 | HG01243.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
missense_variant | MODERATE | c.3422C>T | p.Ala1141Val | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/42 | 3532/6415 | 3422/5424 | 1141/1807 | chr16 | 2080189 | ||
chr16:2080242
|
C | T | 1 | a0017 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.3475C>T | p.Arg1159Trp | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/42 | 3585/6415 | 3475/5424 | 1159/1807 | chr16 | 2080242 | ||
chr16:2083725
|
C | T | 3 | a0006a0008a0011 | 4 | HG02615.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
missense_variant | MODERATE | c.3914C>T | p.Pro1305Leu | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/42 | 4024/6415 | 3914/5424 | 1305/1807 | chr16 | 2083725 | ||
chr16:2083797
|
G | A | 4 | a0004a0007a0012others(1): Show | 8 | HG01070.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
missense_variant | MODERATE | c.3986G>A | p.Arg1329His | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/42 | 4096/6415 | 3986/5424 | 1329/1807 | chr16 | 2083797 | ||
chr16:2084538
|
G | A | 1 | a0012 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.4316G>A | p.Gly1439Asp | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 34/42 | 4426/6415 | 4316/5424 | 1439/1807 | chr16 | 2084538 | ||
chr16:2088073
|
C | A | 1 | a0015 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.5094C>A | p.Ser1698Arg | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 40/42 | 5204/6415 | 5094/5424 | 1698/1807 | chr16 | 2088073 | ||
chr16:2088498
|
C | T | 1 | a0006 | 2 | HG02965.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.5312C>T | p.Pro1771Leu | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 5422/6415 | 5312/5424 | 1771/1807 | chr16 | 2088498 | ||
chr16:2088507
|
G | C | 3 | a0007a0012a0014 | 4 | HG02257.hp1 HG03098.hp2 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.5321G>C | p.Ser1774Thr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 5431/6415 | 5321/5424 | 1774/1807 | chr16 | 2088507 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:2050447
|
G | A | 1 | a0001c0020 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.186G>A | p.Gly62Gly | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/42 | 296/6415 | 186/5424 | 62/1807 | chr16 | 2050447 | ||
chr16:2056226
|
G | A | 1 | a0001c0021 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.630G>A | p.Ala210Ala | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 7/42 | 740/6415 | 630/5424 | 210/1807 | chr16 | 2056226 | ||
chr16:2056721
|
C | T | 1 | a0001c0053 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.726C>T | p.Thr242Thr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 8/42 | 836/6415 | 726/5424 | 242/1807 | chr16 | 2056721 | ||
chr16:2056724
|
C | G | 1 | a0001c0019 | 2 | HG00280.hp1 HG01496.hp2 |
synonymous_variant | LOW | c.729C>G | p.Leu243Leu | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 8/42 | 839/6415 | 729/5424 | 243/1807 | chr16 | 2056724 | ||
chr16:2058846
|
G | A | 1 | a0001c0009 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.948G>A | p.Pro316Pro | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/42 | 1058/6415 | 948/5424 | 316/1807 | chr16 | 2058846 | ||
chr16:2060804
|
G | A | 1 | a0001c0022 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.1110G>A | p.Gln370Gln | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/42 | 1220/6415 | 1110/5424 | 370/1807 | chr16 | 2060804 | ||
chr16:2061921
|
G | A | 1 | a0004c0023 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1170G>A | p.Thr390Thr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 12/42 | 1280/6415 | 1170/5424 | 390/1807 | chr16 | 2061921 | ||
chr16:2062515
|
C | T | 1 | a0001c0052 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1276C>T | p.Leu426Leu | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 13/42 | 1386/6415 | 1276/5424 | 426/1807 | chr16 | 2062515 | ||
chr16:2062553
|
G | A | 1 | a0001c0024 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.1314G>A | p.Lys438Lys | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 13/42 | 1424/6415 | 1314/5424 | 438/1807 | chr16 | 2062553 | ||
chr16:2063032
|
C | T | 1 | a0001c0051 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.1422C>T | p.Leu474Leu | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/42 | 1532/6415 | 1422/5424 | 474/1807 | chr16 | 2063032 | ||
chr16:2064371
|
C | T | 2 | a0001c0050a0007c0018 | 3 | HG02257.hp1 HG03041.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.1543C>T | p.Leu515Leu | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/42 | 1653/6415 | 1543/5424 | 515/1807 | chr16 | 2064371 | ||
chr16:2064406
|
C | T | 3 | a0001c0008a0001c0048a0001c0049 | 6 | HG00140.hp2 HG00639.hp2 HG01346.hp1 others(3): Show |
synonymous_variant | LOW | c.1578C>T | p.Ser526Ser | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/42 | 1688/6415 | 1578/5424 | 526/1807 | chr16 | 2064406 | ||
chr16:2065561
|
A | C | 1 | a0001c0047 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.1642A>C | p.Arg548Arg | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/42 | 1752/6415 | 1642/5424 | 548/1807 | chr16 | 2065561 | ||
chr16:2071539
|
C | T | 1 | a0001c0046 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1869C>T | p.Ala623Ala | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 18/42 | 1979/6415 | 1869/5424 | 623/1807 | chr16 | 2071539 | ||
chr16:2072867
|
C | T | 1 | a0012c0045 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2239C>T | p.Leu747Leu | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/42 | 2349/6415 | 2239/5424 | 747/1807 | chr16 | 2072867 | ||
chr16:2075818
|
C | T | 1 | a0001c0012 | 3 | HG02486.hp1 HG02647.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.2565C>T | p.His855His | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/42 | 2675/6415 | 2565/5424 | 855/1807 | chr16 | 2075818 | ||
chr16:2075833
|
T | C | 6 | a0001c0004a0001c0008a0001c0014others(3): Show | 17 | HG00639.hp2 HG00741.hp2 HG01346.hp1 others(14): Show |
synonymous_variant | LOW | c.2580T>C | p.Phe860Phe | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/42 | 2690/6415 | 2580/5424 | 860/1807 | chr16 | 2075833 | ||
chr16:2079191
|
G | C | 2 | a0001c0007a0001c0032 | 7 | HG01891.hp1 HG02896.hp2 HG02922.hp1 others(4): Show |
synonymous_variant | LOW | c.3126G>C | p.Pro1042Pro | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 27/42 | 3236/6415 | 3126/5424 | 1042/1807 | chr16 | 2079191 | ||
chr16:2079605
|
G | A | 1 | a0009c0044 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.3333G>A | p.Lys1111Lys | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 29/42 | 3443/6415 | 3333/5424 | 1111/1807 | chr16 | 2079605 | ||
chr16:2081752
|
G | A | 1 | a0001c0034 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.3768G>A | p.Pro1256Pro | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/42 | 3878/6415 | 3768/5424 | 1256/1807 | chr16 | 2081752 | ||
chr16:2083726
|
G | A | 2 | a0001c0004a0001c0015 | 10 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(7): Show |
synonymous_variant | LOW | c.3915G>A | p.Pro1305Pro | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/42 | 4025/6415 | 3915/5424 | 1305/1807 | chr16 | 2083726 | ||
chr16:2084437
|
C | T | 1 | a0001c0017 | 2 | HG03491.hp1 HG03492.hp1 |
synonymous_variant | LOW | c.4215C>T | p.Ala1405Ala | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 34/42 | 4325/6415 | 4215/5424 | 1405/1807 | chr16 | 2084437 | ||
chr16:2085298
|
C | T | 1 | a0001c0009 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.4638C>T | p.Ala1546Ala | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/42 | 4748/6415 | 4638/5424 | 1546/1807 | chr16 | 2085298 | ||
chr16:2086246
|
G | C | 1 | a0001c0036 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.4716G>C | p.Thr1572Thr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 37/42 | 4826/6415 | 4716/5424 | 1572/1807 | chr16 | 2086246 | ||
chr16:2086841
|
C | T | 1 | a0001c0016 | 2 | HG02145.hp2 HG02615.hp1 |
synonymous_variant | LOW | c.4959C>T | p.Ser1653Ser | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/42 | 5069/6415 | 4959/5424 | 1653/1807 | chr16 | 2086841 | ||
chr16:2086850
|
C | T | 1 | a0001c0041 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.4968C>T | p.Asp1656Asp | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/42 | 5078/6415 | 4968/5424 | 1656/1807 | chr16 | 2086850 | ||
chr16:2086865
|
C | T | 1 | a0001c0003 | 13 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(10): Show |
synonymous_variant | LOW | c.4983C>T | p.Thr1661Thr | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/42 | 5093/6415 | 4983/5424 | 1661/1807 | chr16 | 2086865 | ||
chr16:2087898
|
G | A | 1 | a0001c0037 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.5025G>A | p.Pro1675Pro | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 39/42 | 5135/6415 | 5025/5424 | 1675/1807 | chr16 | 2087898 | ||
chr16:2088268
|
T | C | 23 | a0001c0002a0001c0003a0001c0004others(20): Show | 94 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(91): Show |
synonymous_variant | LOW | c.5202T>C | p.Asp1734Asp | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 41/42 | 5312/6415 | 5202/5424 | 1734/1807 | chr16 | 2088268 | ||
chr16:2088583
|
G | C | 3 | a0001c0008a0001c0014a0001c0039 | 7 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(4): Show |
synonymous_variant | LOW | c.5397G>C | p.Ser1799Ser | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 5507/6415 | 5397/5424 | 1799/1807 | chr16 | 2088583 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:2048034
|
G | A | 1 | a0001c0001t0017 | 1 | HG00558.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/42 | 582 | chr16 | 2048034 | |||||
chr16:2088636
|
G | A | 4 | a0001c0002t0006a0001c0002t0018a0001c0036t0006others(1): Show | 10 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*26G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 26 | chr16 | 2088636 | |||||
chr16:2088657
|
CAGTGAAA others(5): Show |
C | 1 | a0001c0001t0019 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49_*60delGTGAAATA others(4): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 49 | INFO_REALIGN_3_PRIME | chr16 | 2088657 | ||||
chr16:2088669
|
TAA | T | 3 | a0001c0008t0009a0001c0014t0009a0001c0039t0039 | 7 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*61_*62delAA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 61 | INFO_REALIGN_3_PRIME | chr16 | 2088669 | ||||
chr16:2088713
|
G | C | 1 | a0001c0001t0020 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 103 | chr16 | 2088713 | |||||
chr16:2088737
|
T | C | 2 | a0001c0001t0007a0001c0002t0007 | 8 | HG01257.hp2 HG01258.hp2 HG01261.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*127T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 127 | chr16 | 2088737 | |||||
chr16:2088769
|
G | A | 1 | a0001c0001t0021 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 159 | chr16 | 2088769 | |||||
chr16:2088786
|
C | T | 1 | a0001c0001t0038 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 176 | chr16 | 2088786 | |||||
chr16:2088803
|
T | C | 1 | a0001c0001t0022 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*193T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 193 | chr16 | 2088803 | |||||
chr16:2088866
|
C | T | 1 | a0001c0003t0004 | 12 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*256C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 256 | chr16 | 2088866 | |||||
chr16:2088868
|
C | T | 17 | a0001c0001t0002a0001c0002t0002a0001c0002t0005others(14): Show | 57 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*258C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 258 | chr16 | 2088868 | |||||
chr16:2088872
|
T | TGC | 5 | a0001c0001t0015a0004c0011t0011a0004c0023t0011others(2): Show | 7 | HG00621.hp1 HG01070.hp2 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*271_*272dupGC | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 273 | INFO_REALIGN_3_PRIME | chr16 | 2088872 | ||||
chr16:2088876
|
C | T | 1 | a0001c0001t0034 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 266 | chr16 | 2088876 | |||||
chr16:2088879
|
G | A | 1 | a0001c0050t0035 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 269 | chr16 | 2088879 | |||||
chr16:2088880
|
C | T | 1 | a0015c0040t0033 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*270C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 270 | chr16 | 2088880 | |||||
chr16:2088881
|
G | A | 1 | a0001c0050t0035 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 271 | chr16 | 2088881 | |||||
chr16:2088881
|
G | GCA | 6 | a0001c0001t0003a0001c0001t0017a0001c0051t0003others(3): Show | 28 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*288_*289dupCA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 290 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
G | GCACA | 1 | a0001c0001t0013 | 3 | HG00544.hp1 HG02040.hp2 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*286_*289dupCACA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 290 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
G | GCGCACA | 9 | a0001c0001t0002a0001c0002t0002a0001c0002t0006others(6): Show | 38 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*272_*273insGCACAC | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 273 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
G | GCGCACAC others(1): Show |
4 | a0001c0002t0005a0001c0002t0018a0001c0004t0005others(1): Show | 12 | HG01081.hp1 HG01109.hp2 HG01884.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*272_*273insGCACAC others(2): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 273 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
G | GCGCACAC others(3): Show |
1 | a0003c0006t0036 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272_*273insGCACAC others(4): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 273 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
G | GCGCGCAC others(7): Show |
1 | a0014c0029t0031 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*272_*273insGCGCAC others(8): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 273 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
G | GCGCGCAC others(9): Show |
1 | a0007c0018t0030 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272_*273insGCGCAC others(10): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 273 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
G | GCGCGCGC others(17): Show |
1 | a0007c0018t0032 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272_*273insGCGCGC others(18): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 273 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
GCA | G | 5 | a0001c0001t0016a0001c0001t0026a0001c0002t0016others(2): Show | 7 | HG01928.hp2 HG02300.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*288_*289delCA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 288 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
GCACA | G | 3 | a0001c0003t0004a0001c0008t0009a0001c0014t0009 | 18 | HG00639.hp2 HG00741.hp2 HG01069.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*286_*289delCACA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 286 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088881
|
GCACACA | G | 3 | a0001c0001t0008a0001c0001t0028a0009c0044t0008 | 8 | HG00741.hp1 HG03239.hp1 HG03239.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*284_*289delCACACA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 284 | INFO_REALIGN_3_PRIME | chr16 | 2088881 | ||||
chr16:2088883
|
A | G | 10 | a0001c0001t0010a0001c0003t0010a0001c0007t0012others(7): Show | 15 | HG01070.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*273A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 273 | chr16 | 2088883 | |||||
chr16:2088885
|
A | G | 1 | a0001c0007t0012 | 4 | HG01891.hp1 HG02896.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*275A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 275 | chr16 | 2088885 | |||||
chr16:2088892
|
C | A | 3 | a0001c0001t0016a0001c0002t0016a0001c0003t0004 | 14 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*282C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 282 | chr16 | 2088892 | |||||
chr16:2089126
|
A | T | 31 | a0001c0001t0002a0001c0001t0016a0001c0002t0002others(28): Show | 78 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*516A>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 516 | chr16 | 2089126 | |||||
chr16:2089287
|
C | G | 1 | a0001c0001t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*677C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 677 | chr16 | 2089287 | |||||
chr16:2089304
|
C | T | 1 | a0001c0001t0038 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*694C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 694 | chr16 | 2089304 | |||||
chr16:2089362
|
G | A | 1 | a0001c0001t0023 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 752 | chr16 | 2089362 | |||||
chr16:2089376
|
C | A | 1 | a0001c0009t0014 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*766C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 766 | chr16 | 2089376 | |||||
chr16:2089483
|
G | A | 1 | a0001c0001t0028 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 42/42 | 873 | chr16 | 2089483 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:2048067
|
TAAGTGGC others(14): Show |
T | 1 | a0012c0045t0025g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-30+25_-30+45delAG others(19): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr16 | 2048067 | |||||
chr16:2048199
|
C | T | 1 | a0001c0050t0035g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-30+134C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | chr16 | 2048199 | ||||||
chr16:2048204
|
T | G | 1 | a0001c0052t0001g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-30+139T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | chr16 | 2048204 | ||||||
chr16:2048214
|
T | C | 1 | a0001c0001t0024g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30+149T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | chr16 | 2048214 | ||||||
chr16:2048348
|
C | T | 2 | a0001c0003t0004g0296a0001c0003t0004g0297 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-29-239C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | chr16 | 2048348 | ||||||
chr16:2048498
|
A | T | 1 | a0001c0004t0005g0014 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-29-89A>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | chr16 | 2048498 | ||||||
chr16:2048527
|
A | T | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-29-60A>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | chr16 | 2048527 | ||||||
chr16:2048553
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-29-34C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | chr16 | 2048553 | ||||||
chr16:2048570
|
C | T | 1 | a0001c0017t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-29-17C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | chr16 | 2048570 | ||||||
chr16:2048577
|
G | C | 1 | a0001c0002t0006g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-29-10G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 1/41 | chr16 | 2048577 | ||||||
chr16:2048767
|
C | G | 1 | a0001c0001t0003g0292 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.138+14C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2048767 | ||||||
chr16:2048964
|
T | C | 1 | a0012c0045t0025g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.138+211T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2048964 | ||||||
chr16:2049016
|
C | A | 1 | a0001c0050t0035g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.138+263C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049016 | ||||||
chr16:2049084
|
C | A | 1 | a0001c0001t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.138+331C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049084 | ||||||
chr16:2049093
|
A | AT | 23 | a0001c0001t0001g0273a0001c0002t0002g0276a0001c0002t0002g0279others(20): Show | 25 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.138+350dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr16 | 2049093 | |||||
chr16:2049098
|
T | A | 6 | a0001c0002t0002g0020a0001c0002t0006g0021a0001c0007t0012g0005others(3): Show | 7 | HG01891.hp1 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+345T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049098 | ||||||
chr16:2049180
|
G | A | 5 | a0004c0011t0011g0026a0004c0011t0011g0027a0004c0011t0029g0025others(2): Show | 5 | HG01070.hp2 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+427G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049180 | ||||||
chr16:2049231
|
A | G | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(133): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.138+478A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049231 | ||||||
chr16:2049273
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.138+520A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049273 | ||||||
chr16:2049313
|
TGACCTCA others(7): Show |
T | 5 | a0001c0002t0002g0020a0001c0002t0006g0021a0001c0007t0012g0005others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+561_138+574del others(14): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049313 | ||||||
chr16:2049402
|
A | G | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271others(1): Show | 4 | HG00408.hp1 NA18945.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+649A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049402 | ||||||
chr16:2049425
|
A | G | 12 | a0001c0001t0001g0143a0001c0003t0004g0142a0001c0003t0004g0144others(9): Show | 12 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+672A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049425 | ||||||
chr16:2049528
|
A | G | 3 | a0001c0009t0014g0008a0001c0009t0014g0141a0012c0045t0025g0299 | 4 | HG02723.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+775A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049528 | ||||||
chr16:2049536
|
C | T | 4 | a0001c0002t0006g0021a0001c0007t0012g0005a0001c0007t0012g0022others(1): Show | 5 | HG01891.hp1 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+783C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049536 | ||||||
chr16:2049567
|
G | A | 6 | a0001c0001t0001g0032a0001c0008t0009g0029a0001c0008t0009g0030others(3): Show | 6 | HG00140.hp2 HG00639.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+814G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049567 | ||||||
chr16:2049597
|
G | T | 1 | a0001c0004t0005g0140 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.139-803G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049597 | ||||||
chr16:2049606
|
C | G | 1 | a0015c0040t0033g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.139-794C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049606 | ||||||
chr16:2049694
|
T | C | 1 | a0014c0029t0031g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-706T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049694 | ||||||
chr16:2049718
|
C | T | 3 | a0006c0013t0010g0137a0006c0013t0010g0139a0008c0028t0010g0138 | 3 | HG02965.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.139-682C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2049718 | ||||||
chr16:2049953
|
C | CT | 8 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0265others(5): Show | 8 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-428dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | INFO_REALIGN_3_PRIME | chr16 | 2049953 | |||||
chr16:2050087
|
C | T | 1 | a0014c0029t0031g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-313C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2050087 | ||||||
chr16:2050157
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.139-243A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2050157 | ||||||
chr16:2050240
|
A | G | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.139-160A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 2/41 | chr16 | 2050240 | ||||||
chr16:2050598
|
C | CT | 6 | a0001c0001t0001g0134a0001c0001t0001g0261a0001c0001t0001g0262others(3): Show | 6 | HG01361.hp2 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+133dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | INFO_REALIGN_3_PRIME | chr16 | 2050598 | |||||
chr16:2050598
|
CT | C | 45 | a0001c0001t0001g0054a0001c0001t0001g0135a0001c0001t0001g0143others(42): Show | 46 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.225+133delT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | INFO_REALIGN_3_PRIME | chr16 | 2050598 | |||||
chr16:2050664
|
T | TCACTGCA others(221): Show |
1 | a0001c0001t0001g0261 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.225+184_225+411dup others(228): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | INFO_REALIGN_3_PRIME | chr16 | 2050664 | |||||
chr16:2050878
|
C | T | 5 | a0001c0001t0003g0270a0001c0002t0006g0021a0001c0007t0012g0005others(2): Show | 6 | HG00408.hp1 HG01891.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+392C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2050878 | ||||||
chr16:2050879
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0056a0001c0001t0001g0057 | 5 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+393G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2050879 | ||||||
chr16:2050922
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.225+436G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2050922 | ||||||
chr16:2051145
|
G | A | 4 | a0001c0002t0006g0021a0001c0007t0012g0005a0001c0007t0012g0022others(1): Show | 5 | HG01891.hp1 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+659G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2051145 | ||||||
chr16:2051153
|
G | A | 11 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.225+667G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2051153 | ||||||
chr16:2051483
|
C | T | 5 | a0001c0002t0002g0020a0004c0011t0011g0026a0004c0011t0011g0027others(2): Show | 5 | HG01070.hp2 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+997C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2051483 | ||||||
chr16:2051545
|
T | C | 1 | a0001c0004t0005g0140 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.225+1059T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2051545 | ||||||
chr16:2051546
|
T | C | 1 | a0001c0037t0027g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225+1060T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2051546 | ||||||
chr16:2051590
|
T | C | 17 | a0001c0001t0001g0032a0001c0002t0002g0006a0001c0002t0002g0020others(14): Show | 18 | HG00140.hp2 HG00639.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.225+1104T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2051590 | ||||||
chr16:2051747
|
C | T | 2 | a0001c0001t0001g0132a0011c0042t0002g0133 | 2 | HG01934.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.225+1261C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2051747 | ||||||
chr16:2051748
|
G | A | 23 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0036others(20): Show | 23 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.225+1262G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2051748 | ||||||
chr16:2051933
|
C | T | 4 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0013g0260others(1): Show | 4 | HG02074.hp1 HG02132.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-1409C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2051933 | ||||||
chr16:2052215
|
T | TAAGAGTA others(325): Show |
1 | a0001c0019t0002g0052 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.226-1109_226-1108i others(334): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | INFO_REALIGN_3_PRIME | chr16 | 2052215 | |||||
chr16:2052215
|
T | TAAGAGTA others(326): Show |
21 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0039others(18): Show | 21 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.226-1109_226-1108i others(335): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | INFO_REALIGN_3_PRIME | chr16 | 2052215 | |||||
chr16:2052215
|
T | TAAGAGTA others(327): Show |
2 | a0001c0002t0002g0036a0001c0002t0006g0035 | 2 | HG01433.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.226-1109_226-1108i others(336): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | INFO_REALIGN_3_PRIME | chr16 | 2052215 | |||||
chr16:2052215
|
T | TAAGAGTA others(326): Show |
1 | a0001c0002t0018g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-1109_226-1108i others(335): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | INFO_REALIGN_3_PRIME | chr16 | 2052215 | |||||
chr16:2052255
|
GTTGTCTG others(3): Show |
G | 24 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0036others(21): Show | 24 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.226-1085_226-1076d others(12): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | INFO_REALIGN_3_PRIME | chr16 | 2052255 | |||||
chr16:2052473
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.226-869C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2052473 | ||||||
chr16:2052485
|
T | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(129): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.226-857T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2052485 | ||||||
chr16:2052494
|
G | A | 3 | a0001c0001t0002g0038a0001c0019t0002g0037a0001c0019t0002g0052 | 3 | HG00280.hp1 HG01496.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.226-848G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2052494 | ||||||
chr16:2052610
|
A | G | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(160): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.226-732A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2052610 | ||||||
chr16:2052827
|
C | T | 3 | a0001c0003t0004g0126a0001c0003t0004g0127a0011c0042t0002g0133 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.226-515C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2052827 | ||||||
chr16:2052894
|
C | T | 1 | a0001c0002t0018g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-448C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2052894 | ||||||
chr16:2052949
|
C | G | 1 | a0001c0008t0009g0064 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.226-393C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2052949 | ||||||
chr16:2053004
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0249a0001c0001t0001g0252others(5): Show | 8 | HG01261.hp2 HG01346.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-338C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2053004 | ||||||
chr16:2053136
|
G | A | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.226-206G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2053136 | ||||||
chr16:2053241
|
C | T | 3 | a0001c0002t0002g0036a0001c0002t0002g0051a0001c0002t0005g0050 | 3 | HG01081.hp1 HG01243.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.226-101C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2053241 | ||||||
chr16:2053260
|
C | T | 3 | a0001c0001t0001g0246a0001c0001t0001g0248a0001c0020t0001g0247 | 3 | HG02080.hp1 HG03017.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.226-82C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 3/41 | chr16 | 2053260 | ||||||
chr16:2053485
|
G | T | 2 | a0001c0002t0016g0128a0022c0025t0001g0129 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.336+33G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 4/41 | chr16 | 2053485 | ||||||
chr16:2053685
|
T | C | 1 | a0001c0002t0002g0039 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.336+233T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 4/41 | chr16 | 2053685 | ||||||
chr16:2054233
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.337-63C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 4/41 | chr16 | 2054233 | ||||||
chr16:2054253
|
C | T | 1 | a0001c0002t0002g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.337-43C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 4/41 | chr16 | 2054253 | ||||||
chr16:2054786
|
C | T | 1 | a0015c0040t0033g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.481+346C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2054786 | ||||||
chr16:2054792
|
T | C | 13 | a0001c0001t0001g0143a0001c0003t0004g0142a0001c0003t0004g0144others(10): Show | 13 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.481+352T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2054792 | ||||||
chr16:2054930
|
C | G | 1 | a0001c0001t0001g0125 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.482-472C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2054930 | ||||||
chr16:2054975
|
C | T | 1 | a0001c0001t0008g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.482-427C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2054975 | ||||||
chr16:2055035
|
C | T | 4 | a0001c0001t0001g0242a0005c0010t0001g0243a0005c0010t0001g0244others(1): Show | 4 | HG01192.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-367C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055035 | ||||||
chr16:2055054
|
A | G | 223 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(220): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.482-348A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055054 | ||||||
chr16:2055068
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.482-334G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055068 | ||||||
chr16:2055070
|
G | A | 1 | a0001c0003t0004g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.482-332G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055070 | ||||||
chr16:2055075
|
A | T | 1 | a0001c0001t0019g0241 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.482-327A>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055075 | ||||||
chr16:2055134
|
G | A | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.482-268G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055134 | ||||||
chr16:2055210
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.482-192C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055210 | ||||||
chr16:2055288
|
T | C | 4 | a0001c0001t0016g0295a0001c0002t0006g0040a0001c0002t0016g0128others(1): Show | 4 | HG02300.hp2 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-114T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055288 | ||||||
chr16:2055293
|
G | A | 1 | a0001c0001t0003g0263 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.482-109G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055293 | ||||||
chr16:2055334
|
C | G | 40 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(37): Show | 41 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.482-68C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055334 | ||||||
chr16:2055399
|
C | T | 21 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0036others(18): Show | 21 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.482-3C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055399 | ||||||
chr16:2055562
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.599+43T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | chr16 | 2055562 | ||||||
chr16:2055658
|
C | T | 1 | a0023c0054t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.599+139C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | chr16 | 2055658 | ||||||
chr16:2055667
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0056a0001c0001t0001g0057 | 5 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.599+148C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | chr16 | 2055667 | ||||||
chr16:2055742
|
T | G | 1 | a0001c0001t0001g0168 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.599+223T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | chr16 | 2055742 | ||||||
chr16:2055846
|
G | A | 1 | a0001c0002t0006g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.599+327G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | chr16 | 2055846 | ||||||
chr16:2055876
|
GCAAAACT others(6): Show |
G | 1 | a0001c0003t0004g0144 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.600-314_600-302del others(13): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | INFO_REALIGN_3_PRIME | chr16 | 2055876 | |||||
chr16:2055890
|
C | CA | 48 | a0001c0001t0001g0166a0001c0001t0001g0242a0001c0001t0002g0038others(45): Show | 51 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.600-287dupA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | INFO_REALIGN_3_PRIME | chr16 | 2055890 | |||||
chr16:2055890
|
CA | C | 20 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0157others(17): Show | 20 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.600-287delA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | INFO_REALIGN_3_PRIME | chr16 | 2055890 | |||||
chr16:2055977
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.600-219T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | chr16 | 2055977 | ||||||
chr16:2056112
|
C | T | 3 | a0001c0001t0007g0253a0001c0003t0004g0296a0001c0003t0004g0297 | 3 | HG02109.hp2 HG03688.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.600-84C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 6/41 | chr16 | 2056112 | ||||||
chr16:2056406
|
C | T | 2 | a0007c0018t0030g0122a0007c0018t0032g0123 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.648+162C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 7/41 | chr16 | 2056406 | ||||||
chr16:2056446
|
A | G | 3 | a0007c0018t0030g0122a0007c0018t0032g0123a0014c0029t0031g0034 | 3 | HG02257.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.649-198A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 7/41 | chr16 | 2056446 | ||||||
chr16:2056470
|
G | T | 1 | a0001c0001t0001g0266 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.649-174G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 7/41 | chr16 | 2056470 | ||||||
chr16:2056473
|
C | T | 4 | a0004c0011t0011g0026a0004c0011t0011g0027a0004c0011t0029g0025others(1): Show | 4 | HG01070.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-171C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 7/41 | chr16 | 2056473 | ||||||
chr16:2056824
|
G | A | 2 | a0006c0013t0010g0137a0006c0013t0010g0139 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.774+55G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 8/41 | chr16 | 2056824 | ||||||
chr16:2057185
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18522.hp1 | splice_region_variant&intron_variant | LOW | c.848+7G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057185 | ||||||
chr16:2057212
|
G | C | 1 | a0001c0001t0020g0170 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.848+34G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057212 | ||||||
chr16:2057287
|
G | A | 4 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0174others(1): Show | 4 | HG00408.hp2 NA18941.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+109G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057287 | ||||||
chr16:2057291
|
A | G | 5 | a0001c0007t0002g0041a0001c0007t0002g0042a0001c0007t0012g0005others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+113A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057291 | ||||||
chr16:2057321
|
G | T | 11 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0036others(8): Show | 11 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.848+143G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057321 | ||||||
chr16:2057388
|
C | A | 2 | a0006c0013t0010g0137a0006c0013t0010g0139 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.848+210C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057388 | ||||||
chr16:2057420
|
C | T | 1 | a0015c0040t0033g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848+242C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057420 | ||||||
chr16:2057454
|
C | G | 5 | a0001c0007t0002g0041a0001c0007t0002g0042a0001c0007t0012g0005others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+276C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057454 | ||||||
chr16:2057488
|
C | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0294a0001c0001t0003g0001others(6): Show | 12 | HG00544.hp1 HG00642.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.848+310C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057488 | ||||||
chr16:2057761
|
GCCAGCCC others(21): Show |
G | 1 | a0011c0042t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.848+597_848+624del others(28): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr16 | 2057761 | |||||
chr16:2057776
|
G | GCCCTGCA others(22): Show |
12 | a0001c0001t0001g0068a0001c0001t0001g0157a0001c0001t0001g0158others(9): Show | 12 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.849-736_849-708dup others(29): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr16 | 2057776 | |||||
chr16:2057776
|
GCCCTGCA others(22): Show |
G | 36 | a0001c0001t0001g0010a0001c0001t0001g0152a0001c0001t0001g0166others(33): Show | 38 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.849-736_849-708del others(29): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr16 | 2057776 | |||||
chr16:2057776
|
GCCCTGCA others(51): Show |
G | 13 | a0001c0003t0004g0142a0001c0003t0004g0144a0001c0003t0004g0146others(10): Show | 14 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.849-765_849-708del others(58): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr16 | 2057776 | |||||
chr16:2057805
|
C | T | 1 | a0018c0033t0001g0110 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.848+627C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057805 | ||||||
chr16:2057840
|
C | CATCTCTC others(22): Show |
3 | a0001c0002t0006g0040a0001c0002t0016g0128a0022c0025t0001g0129 | 3 | HG02630.hp2 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.848+690_848+691ins others(29): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | INFO_REALIGN_3_PRIME | chr16 | 2057840 | |||||
chr16:2057865
|
C | T | 1 | a0001c0032t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.848+687C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057865 | ||||||
chr16:2057976
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.849-771C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2057976 | ||||||
chr16:2058329
|
C | T | 4 | a0001c0007t0002g0042a0001c0007t0012g0005a0001c0007t0012g0022others(1): Show | 5 | HG01891.hp1 HG02896.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.849-418C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2058329 | ||||||
chr16:2058366
|
C | T | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.849-381C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2058366 | ||||||
chr16:2058386
|
C | T | 1 | a0001c0022t0001g0109 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.849-361C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2058386 | ||||||
chr16:2058424
|
G | A | 3 | a0001c0002t0006g0040a0001c0002t0016g0128a0022c0025t0001g0129 | 3 | HG02630.hp2 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849-323G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2058424 | ||||||
chr16:2058430
|
C | T | 2 | a0001c0032t0001g0121a0001c0037t0027g0059 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.849-317C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2058430 | ||||||
chr16:2058469
|
G | A | 1 | a0001c0002t0006g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.849-278G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2058469 | ||||||
chr16:2058506
|
C | T | 2 | a0001c0001t0008g0155a0001c0001t0008g0257 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.849-241C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 9/41 | chr16 | 2058506 | ||||||
chr16:2058939
|
C | G | 1 | a0023c0054t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.975+66C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2058939 | ||||||
chr16:2058961
|
C | T | 1 | a0023c0054t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.975+88C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2058961 | ||||||
chr16:2059047
|
C | CTT | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(134): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.975+187_975+188dup others(2): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | INFO_REALIGN_3_PRIME | chr16 | 2059047 | |||||
chr16:2059048
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.975+175T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059048 | ||||||
chr16:2059087
|
T | C | 3 | a0007c0018t0030g0122a0007c0018t0032g0123a0014c0029t0031g0034 | 3 | HG02257.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.975+214T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059087 | ||||||
chr16:2059162
|
G | A | 6 | a0001c0002t0002g0020a0004c0011t0011g0026a0004c0011t0011g0027others(3): Show | 6 | HG01070.hp2 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+289G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059162 | ||||||
chr16:2059237
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0230 | 2 | NA18970.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.975+364C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059237 | ||||||
chr16:2059251
|
G | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(160): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.975+378G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059251 | ||||||
chr16:2059273
|
C | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0175 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.975+400C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059273 | ||||||
chr16:2059307
|
C | T | 1 | a0014c0029t0031g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.975+434C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059307 | ||||||
chr16:2059328
|
T | C | 1 | a0001c0048t0001g0028 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.975+455T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059328 | ||||||
chr16:2059328
|
TTCTC | T | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.975+463_975+466del others(4): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | INFO_REALIGN_3_PRIME | chr16 | 2059328 | |||||
chr16:2059338
|
C | CT | 14 | a0001c0001t0003g0108a0001c0001t0003g0292a0001c0001t0016g0295others(11): Show | 14 | HG01109.hp1 HG01258.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.975+486dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | INFO_REALIGN_3_PRIME | chr16 | 2059338 | |||||
chr16:2059338
|
CT | C | 11 | a0001c0001t0001g0157a0001c0001t0001g0179a0001c0001t0003g0178others(8): Show | 11 | HG00099.hp1 HG01257.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.975+486delT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | INFO_REALIGN_3_PRIME | chr16 | 2059338 | |||||
chr16:2059340
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0017g0176a0001c0003t0010g0145 | 3 | HG00558.hp1 NA19004.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.975+467T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059340 | ||||||
chr16:2059421
|
C | T | 1 | a0023c0054t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.975+548C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059421 | ||||||
chr16:2059439
|
T | G | 5 | a0001c0007t0002g0041a0001c0007t0002g0042a0001c0007t0012g0005others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+566T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059439 | ||||||
chr16:2059494
|
A | G | 8 | a0001c0002t0002g0006a0001c0002t0002g0060a0001c0002t0002g0061others(5): Show | 9 | HG01884.hp1 HG02055.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.975+621A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059494 | ||||||
chr16:2059509
|
G | GT | 152 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(149): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.975+660dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | INFO_REALIGN_3_PRIME | chr16 | 2059509 | |||||
chr16:2059509
|
G | GTT | 14 | a0001c0001t0001g0004a0001c0001t0001g0154a0001c0001t0001g0221others(11): Show | 15 | HG00544.hp1 HG00621.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.975+659_975+660dup others(2): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | INFO_REALIGN_3_PRIME | chr16 | 2059509 | |||||
chr16:2059509
|
GT | G | 18 | a0001c0001t0001g0071a0001c0001t0001g0107a0001c0001t0001g0175others(15): Show | 18 | HG01070.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.975+660delT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | INFO_REALIGN_3_PRIME | chr16 | 2059509 | |||||
chr16:2059518
|
T | G | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.975+645T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059518 | ||||||
chr16:2059533
|
T | A | 4 | a0001c0007t0002g0042a0001c0007t0012g0005a0001c0007t0012g0022others(1): Show | 5 | HG01891.hp1 HG02896.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+660T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059533 | ||||||
chr16:2059845
|
G | T | 1 | a0005c0010t0001g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.976-825G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059845 | ||||||
chr16:2059952
|
C | T | 18 | a0001c0001t0001g0058a0001c0001t0001g0067a0001c0001t0001g0095others(15): Show | 18 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.976-718C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059952 | ||||||
chr16:2059992
|
C | A | 1 | a0023c0054t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.976-678C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2059992 | ||||||
chr16:2060175
|
G | A | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.976-495G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2060175 | ||||||
chr16:2060262
|
G | T | 1 | a0001c0001t0001g0154 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.976-408G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2060262 | ||||||
chr16:2060305
|
A | AC | 24 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0068others(21): Show | 24 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.976-359dupC | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | INFO_REALIGN_3_PRIME | chr16 | 2060305 | |||||
chr16:2060309
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.976-361C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2060309 | ||||||
chr16:2060570
|
C | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(149): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.976-100C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2060570 | ||||||
chr16:2060607
|
G | A | 6 | a0001c0008t0009g0029a0001c0008t0009g0030a0001c0008t0009g0033others(3): Show | 6 | HG00140.hp2 HG00639.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.976-63G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2060607 | ||||||
chr16:2060616
|
C | T | 6 | a0001c0002t0002g0020a0004c0011t0011g0026a0004c0011t0011g0027others(3): Show | 6 | HG01070.hp2 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-54C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2060616 | ||||||
chr16:2060626
|
G | A | 1 | a0001c0050t0035g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.976-44G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 10/41 | chr16 | 2060626 | ||||||
chr16:2061046
|
C | T | 1 | a0001c0050t0035g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1119+233C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061046 | ||||||
chr16:2061229
|
A | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1119+416A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061229 | ||||||
chr16:2061253
|
C | T | 1 | a0001c0032t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1119+440C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061253 | ||||||
chr16:2061260
|
A | G | 1 | a0001c0001t0003g0270 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1119+447A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061260 | ||||||
chr16:2061272
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1119+459C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061272 | ||||||
chr16:2061392
|
C | T | 1 | a0023c0054t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1120-479C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061392 | ||||||
chr16:2061570
|
G | A | 4 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0174others(1): Show | 4 | HG00408.hp2 NA18941.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120-301G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061570 | ||||||
chr16:2061709
|
C | T | 6 | a0001c0002t0002g0020a0004c0011t0011g0026a0004c0011t0011g0027others(3): Show | 6 | HG01070.hp2 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-162C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061709 | ||||||
chr16:2061713
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1120-158G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061713 | ||||||
chr16:2061778
|
T | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(163): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1120-93T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 11/41 | chr16 | 2061778 | ||||||
chr16:2062395
|
G | A | 1 | a0001c0002t0006g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1258-102G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 12/41 | chr16 | 2062395 | ||||||
chr16:2062416
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1258-81C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 12/41 | chr16 | 2062416 | ||||||
chr16:2062616
|
T | G | 3 | a0001c0002t0002g0061a0001c0002t0002g0062a0001c0002t0002g0063 | 3 | HG01884.hp1 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1361+16T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 13/41 | chr16 | 2062616 | ||||||
chr16:2062618
|
G | C | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1361+18G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 13/41 | chr16 | 2062618 | ||||||
chr16:2062620
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1361+20C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 13/41 | chr16 | 2062620 | ||||||
chr16:2062682
|
G | T | 1 | a0001c0001t0003g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1361+82G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 13/41 | chr16 | 2062682 | ||||||
chr16:2062940
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1362-32C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 13/41 | chr16 | 2062940 | ||||||
chr16:2063071
|
C | T | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1443+18C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063071 | ||||||
chr16:2063118
|
T | G | 1 | a0001c0002t0016g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1443+65T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063118 | ||||||
chr16:2063129
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1443+76C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063129 | ||||||
chr16:2063191
|
G | A | 2 | a0001c0001t0001g0249a0002c0005t0003g0104 | 2 | HG02273.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1443+138G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063191 | ||||||
chr16:2063212
|
A | G | 1 | a0001c0002t0002g0288 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1443+159A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063212 | ||||||
chr16:2063255
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1443+202C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063255 | ||||||
chr16:2063308
|
C | T | 4 | a0001c0002t0002g0006a0001c0002t0002g0060a0001c0002t0002g0061others(1): Show | 5 | HG01884.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1443+255C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063308 | ||||||
chr16:2063309
|
G | A | 10 | a0001c0003t0004g0142a0001c0003t0004g0144a0001c0003t0004g0146others(7): Show | 10 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1443+256G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063309 | ||||||
chr16:2063324
|
C | G | 1 | a0001c0001t0001g0094 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1443+271C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063324 | ||||||
chr16:2063423
|
G | A | 1 | a0001c0002t0006g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1443+370G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063423 | ||||||
chr16:2063436
|
C | G | 1 | a0001c0003t0004g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1443+383C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063436 | ||||||
chr16:2063583
|
C | T | 10 | a0001c0003t0004g0142a0001c0003t0004g0144a0001c0003t0004g0146others(7): Show | 10 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1443+530C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063583 | ||||||
chr16:2063614
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1443+561G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063614 | ||||||
chr16:2063642
|
C | G | 5 | a0004c0011t0011g0026a0004c0011t0011g0027a0004c0011t0029g0025others(2): Show | 5 | HG01070.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1443+589C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063642 | ||||||
chr16:2063660
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1443+607C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063660 | ||||||
chr16:2063839
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1444-433C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063839 | ||||||
chr16:2063851
|
C | T | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1444-421C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063851 | ||||||
chr16:2063989
|
G | A | 4 | a0001c0009t0014g0008a0001c0009t0014g0141a0012c0045t0025g0299others(1): Show | 5 | HG02723.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1444-283G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2063989 | ||||||
chr16:2064032
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1444-240G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2064032 | ||||||
chr16:2064040
|
C | T | 3 | a0001c0050t0035g0298a0007c0018t0030g0122a0007c0018t0032g0123 | 3 | HG02257.hp1 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1444-232C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2064040 | ||||||
chr16:2064071
|
G | A | 14 | a0001c0002t0002g0276a0001c0002t0002g0279a0001c0002t0002g0280others(11): Show | 16 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1444-201G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2064071 | ||||||
chr16:2064121
|
C | T | 2 | a0012c0045t0025g0299a0014c0029t0031g0034 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1444-151C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2064121 | ||||||
chr16:2064172
|
A | G | 4 | a0001c0009t0014g0008a0001c0009t0014g0141a0012c0045t0025g0299others(1): Show | 5 | HG02723.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1444-100A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 14/41 | chr16 | 2064172 | ||||||
chr16:2064503
|
GTCC | G | 5 | a0001c0007t0002g0041a0001c0007t0002g0042a0001c0007t0012g0005others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1599+82_1599+84del others(3): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | INFO_REALIGN_3_PRIME | chr16 | 2064503 | |||||
chr16:2064572
|
C | T | 1 | a0001c0001t0015g0118 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1599+145C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2064572 | ||||||
chr16:2064586
|
G | C | 1 | a0001c0001t0003g0231 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1599+159G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2064586 | ||||||
chr16:2064589
|
C | T | 1 | a0001c0002t0002g0288 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1599+162C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2064589 | ||||||
chr16:2064643
|
T | G | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0112others(3): Show | 6 | HG00733.hp1 HG01106.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1599+216T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2064643 | ||||||
chr16:2064696
|
C | CCTGGGG | 6 | a0001c0008t0009g0029a0001c0008t0009g0030a0001c0008t0009g0033others(3): Show | 6 | HG00140.hp2 HG00639.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1599+278_1599+283d others(8): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | INFO_REALIGN_3_PRIME | chr16 | 2064696 | |||||
chr16:2064697
|
C | T | 1 | a0001c0001t0010g0156 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1599+270C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2064697 | ||||||
chr16:2064794
|
T | C | 3 | a0007c0018t0030g0122a0007c0018t0032g0123a0014c0029t0031g0034 | 3 | HG02257.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1599+367T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2064794 | ||||||
chr16:2064930
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1599+503A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2064930 | ||||||
chr16:2064942
|
T | C | 1 | a0024c0055t0003g0187 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1599+515T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2064942 | ||||||
chr16:2064945
|
C | T | 1 | a0001c0002t0016g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1599+518C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2064945 | ||||||
chr16:2065032
|
T | C | 5 | a0001c0001t0001g0188a0001c0001t0038g0177a0001c0002t0007g0159others(2): Show | 5 | HG00099.hp1 HG01255.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1600-487T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2065032 | ||||||
chr16:2065039
|
A | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0217a0001c0001t0001g0223others(18): Show | 21 | HG00609.hp1 HG01109.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1600-480A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2065039 | ||||||
chr16:2065096
|
A | G | 1 | a0014c0029t0031g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1600-423A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2065096 | ||||||
chr16:2065209
|
C | T | 16 | a0001c0001t0001g0093a0001c0003t0004g0142a0001c0003t0004g0144others(13): Show | 16 | HG01070.hp2 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1600-310C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2065209 | ||||||
chr16:2065412
|
C | CA | 17 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0076others(14): Show | 18 | HG00741.hp1 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1600-83dupA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | INFO_REALIGN_3_PRIME | chr16 | 2065412 | |||||
chr16:2065412
|
CA | C | 10 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0240others(7): Show | 11 | HG00280.hp2 HG00741.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1600-83delA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | INFO_REALIGN_3_PRIME | chr16 | 2065412 | |||||
chr16:2065412
|
CAA | C | 46 | a0001c0001t0001g0093a0001c0001t0002g0038a0001c0001t0002g0047others(43): Show | 47 | HG00280.hp1 HG01070.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.1600-84_1600-83del others(2): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | INFO_REALIGN_3_PRIME | chr16 | 2065412 | |||||
chr16:2065412
|
CAAA | C | 6 | a0001c0003t0004g0150a0001c0007t0002g0041a0001c0007t0002g0042others(3): Show | 7 | HG01891.hp1 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1600-85_1600-83del others(3): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | INFO_REALIGN_3_PRIME | chr16 | 2065412 | |||||
chr16:2065412
|
CAAAAAAA others(8): Show |
C | 10 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(7): Show | 10 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1600-97_1600-83del others(15): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | INFO_REALIGN_3_PRIME | chr16 | 2065412 | |||||
chr16:2065455
|
T | G | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1600-64T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2065455 | ||||||
chr16:2065463
|
C | G | 2 | a0001c0001t0016g0295a0001c0002t0016g0128 | 2 | HG02300.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1600-56C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2065463 | ||||||
chr16:2065480
|
C | T | 11 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0036others(8): Show | 11 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1600-39C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2065480 | ||||||
chr16:2065505
|
C | T | 6 | a0001c0008t0009g0029a0001c0008t0009g0030a0001c0008t0009g0033others(3): Show | 6 | HG00140.hp2 HG00639.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1600-14C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 15/41 | chr16 | 2065505 | ||||||
chr16:2065717
|
T | C | 2 | a0012c0045t0025g0299a0014c0029t0031g0034 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1716+82T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2065717 | ||||||
chr16:2065818
|
A | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1716+183A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2065818 | ||||||
chr16:2065856
|
T | C | 17 | a0001c0001t0024g0016a0001c0002t0002g0020a0001c0002t0006g0017others(14): Show | 17 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1716+221T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2065856 | ||||||
chr16:2066052
|
T | A | 1 | a0001c0001t0022g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1716+417T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066052 | ||||||
chr16:2066082
|
A | C | 36 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(33): Show | 38 | HG00642.hp1 HG01099.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.1716+447A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066082 | ||||||
chr16:2066397
|
T | C | 12 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(9): Show | 12 | HG00642.hp1 HG01099.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1716+762T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066397 | ||||||
chr16:2066403
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1716+768C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066403 | ||||||
chr16:2066651
|
C | CT | 72 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(69): Show | 75 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1716+1040dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2066651 | |||||
chr16:2066651
|
C | CTT | 7 | a0001c0001t0001g0217a0001c0001t0001g0242a0001c0001t0003g0108others(4): Show | 7 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(4): Show |
intron_variant | MODIFIER | c.1716+1039_1716+104 others(6): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2066651 | |||||
chr16:2066651
|
CT | C | 27 | a0001c0001t0001g0065a0001c0001t0001g0120a0001c0001t0001g0136others(24): Show | 27 | HG00280.hp1 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1716+1040delT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2066651 | |||||
chr16:2066651
|
CTT | C | 37 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(34): Show | 38 | HG00642.hp1 HG01099.hp2 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.1716+1039_1716+104 others(6): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2066651 | |||||
chr16:2066651
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1716+1030_1716+104 others(15): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2066651 | |||||
chr16:2066679
|
A | G | 1 | a0001c0001t0010g0156 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1716+1044A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066679 | ||||||
chr16:2066721
|
C | T | 1 | a0004c0011t0029g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1716+1086C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066721 | ||||||
chr16:2066724
|
G | A | 16 | a0001c0002t0002g0020a0001c0002t0006g0017a0001c0002t0006g0021others(13): Show | 16 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1716+1089G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066724 | ||||||
chr16:2066817
|
T | C | 41 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(38): Show | 43 | HG00642.hp1 HG01099.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1716+1182T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066817 | ||||||
chr16:2066818
|
A | G | 1 | a0001c0050t0035g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1716+1183A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066818 | ||||||
chr16:2066929
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1716+1294T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066929 | ||||||
chr16:2066953
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1716+1318C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066953 | ||||||
chr16:2066979
|
G | C | 33 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(30): Show | 34 | HG00642.hp1 HG01099.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.1716+1344G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066979 | ||||||
chr16:2066985
|
C | G | 1 | a0001c0001t0001g0262 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1716+1350C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2066985 | ||||||
chr16:2067020
|
C | T | 2 | a0007c0018t0030g0122a0007c0018t0032g0123 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1716+1385C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067020 | ||||||
chr16:2067148
|
T | A | 1 | a0001c0002t0016g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1716+1513T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067148 | ||||||
chr16:2067259
|
A | G | 2 | a0001c0001t0016g0295a0001c0002t0016g0128 | 2 | HG02300.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1716+1624A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067259 | ||||||
chr16:2067265
|
C | T | 1 | a0001c0001t0003g0235 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1716+1630C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067265 | ||||||
chr16:2067438
|
A | G | 2 | a0001c0001t0003g0198a0012c0045t0025g0299 | 2 | HG00544.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1716+1803A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067438 | ||||||
chr16:2067524
|
A | ATG | 10 | a0001c0003t0004g0144a0001c0003t0004g0146a0001c0003t0004g0147others(7): Show | 10 | HG02109.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1716+1889_1716+189 others(6): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067524 | ||||||
chr16:2067525
|
C | A | 10 | a0001c0003t0004g0144a0001c0003t0004g0146a0001c0003t0004g0147others(7): Show | 10 | HG02109.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1716+1890C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067525 | ||||||
chr16:2067526
|
T | A | 1 | a0001c0002t0018g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1716+1891T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067526 | ||||||
chr16:2067526
|
T | G | 10 | a0001c0003t0004g0144a0001c0003t0004g0146a0001c0003t0004g0147others(7): Show | 10 | HG02109.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1716+1891T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067526 | ||||||
chr16:2067527
|
T | C | 10 | a0001c0003t0004g0144a0001c0003t0004g0146a0001c0003t0004g0147others(7): Show | 10 | HG02109.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1716+1892T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067527 | ||||||
chr16:2067558
|
G | A | 1 | a0001c0008t0009g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1716+1923G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067558 | ||||||
chr16:2067639
|
G | A | 15 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(12): Show | 15 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1716+2004G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067639 | ||||||
chr16:2067702
|
A | G | 11 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(8): Show | 11 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1716+2067A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067702 | ||||||
chr16:2067744
|
T | C | 1 | a0011c0042t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1716+2109T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067744 | ||||||
chr16:2067833
|
G | A | 1 | a0001c0002t0006g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1716+2198G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067833 | ||||||
chr16:2067854
|
A | T | 1 | a0001c0037t0027g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1716+2219A>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2067854 | ||||||
chr16:2068018
|
G | C | 11 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(8): Show | 11 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1716+2383G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068018 | ||||||
chr16:2068158
|
G | C | 1 | a0012c0045t0025g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1717-2298G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068158 | ||||||
chr16:2068187
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1717-2269G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068187 | ||||||
chr16:2068223
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1717-2233A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068223 | ||||||
chr16:2068485
|
T | C | 15 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(12): Show | 15 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1717-1971T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068485 | ||||||
chr16:2068535
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1717-1921T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068535 | ||||||
chr16:2068566
|
G | A | 18 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(15): Show | 19 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1717-1890G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068566 | ||||||
chr16:2068724
|
T | C | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1717-1732T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068724 | ||||||
chr16:2068740
|
G | C | 11 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(8): Show | 11 | HG00642.hp1 HG01099.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.1717-1716G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068740 | ||||||
chr16:2068740
|
G | T | 5 | a0001c0007t0002g0041a0001c0007t0002g0042a0001c0007t0012g0005others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1717-1716G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068740 | ||||||
chr16:2068835
|
A | G | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(164): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1717-1621A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068835 | ||||||
chr16:2068868
|
G | A | 1 | a0001c0004t0005g0140 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1717-1588G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068868 | ||||||
chr16:2068872
|
C | CA | 13 | a0001c0001t0001g0152a0001c0001t0001g0175a0001c0001t0001g0259others(10): Show | 14 | HG00741.hp1 HG01175.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1717-1563dupA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2068872 | |||||
chr16:2068872
|
C | CAA | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(131): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1717-1564_1717-156 others(6): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2068872 | |||||
chr16:2068872
|
C | CAAA | 24 | a0001c0001t0001g0115a0001c0001t0001g0181a0001c0001t0001g0182others(21): Show | 25 | HG00544.hp1 HG00735.hp1 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.1717-1565_1717-156 others(7): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2068872 | |||||
chr16:2068872
|
CA | C | 23 | a0001c0001t0001g0054a0001c0001t0001g0090a0001c0001t0001g0091others(20): Show | 23 | HG02015.hp2 HG02109.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1717-1563delA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2068872 | |||||
chr16:2068897
|
TAAGG | T | 9 | a0001c0003t0004g0142a0001c0003t0004g0144a0001c0003t0004g0146others(6): Show | 9 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1717-1555_1717-155 others(8): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2068897 | |||||
chr16:2068905
|
C | A | 1 | a0001c0012t0001g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1717-1551C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068905 | ||||||
chr16:2068942
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1717-1514C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2068942 | ||||||
chr16:2069169
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0132 | 3 | HG01074.hp2 HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1717-1287C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069169 | ||||||
chr16:2069186
|
T | C | 67 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(64): Show | 69 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1717-1270T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069186 | ||||||
chr16:2069202
|
A | C | 15 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(12): Show | 15 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1717-1254A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069202 | ||||||
chr16:2069251
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0162a0001c0001t0034g0160 | 3 | HG02258.hp1 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1717-1205T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069251 | ||||||
chr16:2069314
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1717-1142C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069314 | ||||||
chr16:2069367
|
A | C | 1 | a0001c0001t0001g0221 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1717-1089A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069367 | ||||||
chr16:2069467
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1717-989A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069467 | ||||||
chr16:2069484
|
A | AT | 19 | a0001c0001t0001g0117a0001c0001t0001g0211a0001c0001t0003g0108others(16): Show | 19 | HG02074.hp2 HG02280.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1717-957dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2069484 | |||||
chr16:2069486
|
T | TTTTTTTT others(304): Show |
1 | a0001c0001t0001g0265 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1717-957_1717-956i others(313): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2069486 | |||||
chr16:2069515
|
T | C | 12 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0001t0024g0016others(9): Show | 12 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1717-941T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069515 | ||||||
chr16:2069643
|
C | A | 1 | a0001c0008t0009g0064 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1717-813C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069643 | ||||||
chr16:2069681
|
C | T | 11 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0001g0157others(8): Show | 11 | HG00642.hp1 HG01099.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.1717-775C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069681 | ||||||
chr16:2069701
|
T | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0181a0001c0015t0005g0277others(1): Show | 4 | HG01109.hp2 NA18962.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1717-755T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069701 | ||||||
chr16:2069726
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1717-730C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069726 | ||||||
chr16:2069735
|
T | C | 11 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0001g0157others(8): Show | 11 | HG00642.hp1 HG01099.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.1717-721T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069735 | ||||||
chr16:2069741
|
A | G | 5 | a0001c0007t0002g0041a0001c0007t0002g0042a0001c0007t0012g0005others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1717-715A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069741 | ||||||
chr16:2069769
|
T | C | 11 | a0001c0003t0004g0142a0001c0003t0004g0144a0001c0003t0004g0146others(8): Show | 11 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1717-687T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069769 | ||||||
chr16:2069770
|
G | A | 10 | a0001c0003t0004g0142a0001c0003t0004g0144a0001c0003t0004g0146others(7): Show | 10 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1717-686G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069770 | ||||||
chr16:2069771
|
T | C | 10 | a0001c0003t0004g0142a0001c0003t0004g0144a0001c0003t0004g0146others(7): Show | 10 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1717-685T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069771 | ||||||
chr16:2069775
|
C | T | 2 | a0001c0001t0001g0120a0018c0033t0001g0110 | 2 | NA18997.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1717-681C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069775 | ||||||
chr16:2069869
|
T | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0174 | 3 | NA18941.hp1 NA18961.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1717-587T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069869 | ||||||
chr16:2069942
|
C | T | 4 | a0001c0050t0035g0298a0007c0018t0030g0122a0007c0018t0032g0123others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-514C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2069942 | ||||||
chr16:2070010
|
A | C | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1717-446A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2070010 | ||||||
chr16:2070099
|
AC | A | 18 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0024g0016others(15): Show | 19 | HG01070.hp2 HG01891.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1717-356delC | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2070099 | ||||||
chr16:2070153
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1717-303C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2070153 | ||||||
chr16:2070229
|
T | C | 2 | a0001c0002t0007g0159a0001c0002t0007g0163 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1717-227T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2070229 | ||||||
chr16:2070299
|
GGA | G | 8 | a0001c0001t0034g0160a0001c0003t0004g0151a0004c0011t0011g0026others(5): Show | 8 | HG01070.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1717-149_1717-148d others(4): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | INFO_REALIGN_3_PRIME | chr16 | 2070299 | |||||
chr16:2070368
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1717-88C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2070368 | ||||||
chr16:2070389
|
A | G | 2 | a0001c0015t0005g0278a0022c0025t0001g0129 | 2 | HG01109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1717-67A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2070389 | ||||||
chr16:2070401
|
T | C | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0054others(115): Show | 125 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(122): Show |
intron_variant | MODIFIER | c.1717-55T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 16/41 | chr16 | 2070401 | ||||||
chr16:2070732
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1839+154C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070732 | ||||||
chr16:2070784
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1839+206C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070784 | ||||||
chr16:2070826
|
C | T | 1 | a0001c0002t0006g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1839+248C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070826 | ||||||
chr16:2070840
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0130 | 2 | HG01496.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1839+262C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070840 | ||||||
chr16:2070919
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1839+341G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070919 | ||||||
chr16:2070945
|
A | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0248a0001c0020t0001g0247 | 3 | HG02080.hp1 HG03017.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1839+367A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070945 | ||||||
chr16:2070979
|
A | G | 13 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(10): Show | 13 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1839+401A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070979 | ||||||
chr16:2070982
|
T | A | 13 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(10): Show | 13 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1839+404T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070982 | ||||||
chr16:2070984
|
A | G | 13 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(10): Show | 13 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1839+406A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070984 | ||||||
chr16:2070986
|
A | AT | 13 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(10): Show | 13 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1839+408_1839+409i others(3): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070986 | ||||||
chr16:2070993
|
G | A | 13 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(10): Show | 13 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1839+415G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070993 | ||||||
chr16:2070994
|
G | A | 13 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(10): Show | 13 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1839+416G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2070994 | ||||||
chr16:2071000
|
A | ATGGGCAG others(8): Show |
5 | a0001c0009t0014g0008a0001c0009t0014g0141a0006c0013t0010g0137others(2): Show | 6 | HG02723.hp2 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1839+426_1839+440d others(17): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | INFO_REALIGN_3_PRIME | chr16 | 2071000 | |||||
chr16:2071000
|
A | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(149): Show | 159 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1839+422A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071000 | ||||||
chr16:2071068
|
A | G | 5 | a0004c0011t0011g0026a0004c0011t0011g0027a0004c0011t0029g0025others(2): Show | 5 | HG01070.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1840-442A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071068 | ||||||
chr16:2071153
|
G | A | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(2): Show | 5 | HG00140.hp1 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1840-357G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071153 | ||||||
chr16:2071187
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1840-323C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071187 | ||||||
chr16:2071193
|
C | T | 3 | a0006c0013t0010g0137a0006c0013t0010g0139a0008c0028t0010g0138 | 3 | HG02965.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1840-317C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071193 | ||||||
chr16:2071224
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0015g0118 | 3 | NA18983.hp2 NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1840-286G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071224 | ||||||
chr16:2071338
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1840-172G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071338 | ||||||
chr16:2071374
|
T | C | 5 | a0001c0002t0002g0020a0001c0007t0012g0005a0001c0007t0012g0022others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1840-136T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071374 | ||||||
chr16:2071420
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1840-90G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071420 | ||||||
chr16:2071425
|
G | A | 1 | a0001c0032t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1840-85G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071425 | ||||||
chr16:2071472
|
G | A | 1 | a0001c0001t0024g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1840-38G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 17/41 | chr16 | 2071472 | ||||||
chr16:2071780
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0271 | 2 | NA18945.hp2 NA18966.hp2 |
splice_region_variant&intron_variant | LOW | c.1947-4G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 18/41 | chr16 | 2071780 | ||||||
chr16:2071982
|
G | T | 1 | a0012c0045t0025g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2097+48G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 19/41 | chr16 | 2071982 | ||||||
chr16:2072038
|
C | T | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2097+104C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 19/41 | chr16 | 2072038 | ||||||
chr16:2072115
|
C | G | 1 | a0001c0053t0001g0169 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2098-126C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 19/41 | chr16 | 2072115 | ||||||
chr16:2072127
|
A | G | 30 | a0001c0001t0016g0295a0001c0002t0002g0282a0001c0002t0006g0017others(27): Show | 34 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(31): Show |
intron_variant | MODIFIER | c.2098-114A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 19/41 | chr16 | 2072127 | ||||||
chr16:2072388
|
G | C | 1 | a0012c0045t0025g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2220+25G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 20/41 | chr16 | 2072388 | ||||||
chr16:2072545
|
C | T | 17 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0001g0162others(14): Show | 17 | HG01515.hp1 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2220+182C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 20/41 | chr16 | 2072545 | ||||||
chr16:2072821
|
A | G | 30 | a0001c0001t0016g0295a0001c0002t0002g0282a0001c0002t0006g0017others(27): Show | 34 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(31): Show |
intron_variant | MODIFIER | c.2221-28A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 20/41 | chr16 | 2072821 | ||||||
chr16:2072823
|
G | A | 3 | a0006c0013t0010g0137a0006c0013t0010g0139a0008c0028t0010g0138 | 3 | HG02965.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2221-26G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 20/41 | chr16 | 2072823 | ||||||
chr16:2073136
|
A | G | 1 | a0001c0037t0027g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2355+153A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/41 | chr16 | 2073136 | ||||||
chr16:2073149
|
C | T | 1 | a0001c0002t0002g0288 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2355+166C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/41 | chr16 | 2073149 | ||||||
chr16:2073151
|
G | A | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2355+168G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/41 | chr16 | 2073151 | ||||||
chr16:2073242
|
G | GT | 9 | a0001c0001t0016g0295a0001c0002t0002g0282a0001c0002t0016g0128others(6): Show | 11 | HG01884.hp2 HG02300.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2355+261dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/41 | INFO_REALIGN_3_PRIME | chr16 | 2073242 | |||||
chr16:2073461
|
C | T | 12 | a0001c0002t0002g0051a0001c0003t0004g0142a0001c0003t0004g0144others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2355+478C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/41 | chr16 | 2073461 | ||||||
chr16:2073830
|
G | A | 1 | a0001c0001t0017g0176 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2356-370G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/41 | chr16 | 2073830 | ||||||
chr16:2073967
|
G | A | 1 | a0001c0047t0001g0079 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2356-233G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/41 | chr16 | 2073967 | ||||||
chr16:2074024
|
G | T | 3 | a0001c0009t0014g0008a0001c0009t0014g0141a0001c0037t0027g0059 | 4 | HG02723.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2356-176G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/41 | chr16 | 2074024 | ||||||
chr16:2074102
|
C | T | 1 | a0001c0032t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2356-98C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 21/41 | chr16 | 2074102 | ||||||
chr16:2074420
|
C | T | 1 | a0001c0002t0006g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2545+31C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074420 | ||||||
chr16:2074447
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2545+58C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074447 | ||||||
chr16:2074480
|
T | TG | 15 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(12): Show | 16 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2545+95dupG | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr16 | 2074480 | |||||
chr16:2074524
|
C | T | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2545+135C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074524 | ||||||
chr16:2074531
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2545+142G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074531 | ||||||
chr16:2074546
|
G | C | 12 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(9): Show | 12 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2545+157G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074546 | ||||||
chr16:2074583
|
A | G | 10 | a0001c0001t0016g0295a0001c0002t0002g0282a0001c0002t0016g0128others(7): Show | 12 | HG01884.hp2 HG02300.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2545+194A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074583 | ||||||
chr16:2074629
|
C | T | 12 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(9): Show | 12 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2545+240C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074629 | ||||||
chr16:2074633
|
C | A | 1 | a0012c0045t0025g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2545+244C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074633 | ||||||
chr16:2074633
|
C | G | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2545+244C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074633 | ||||||
chr16:2074725
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2545+336T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074725 | ||||||
chr16:2074856
|
G | A | 1 | a0001c0002t0016g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2545+467G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074856 | ||||||
chr16:2074907
|
G | T | 9 | a0001c0001t0016g0295a0001c0002t0002g0282a0001c0002t0016g0128others(6): Show | 11 | HG01884.hp2 HG02300.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2545+518G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074907 | ||||||
chr16:2074943
|
C | A | 5 | a0004c0011t0011g0026a0004c0011t0011g0027a0004c0011t0029g0025others(2): Show | 5 | HG01070.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2545+554C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074943 | ||||||
chr16:2074944
|
G | A | 1 | a0001c0003t0004g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2545+555G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074944 | ||||||
chr16:2074963
|
C | G | 1 | a0001c0008t0009g0064 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2545+574C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2074963 | ||||||
chr16:2075132
|
A | C | 1 | a0001c0014t0009g0049 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2546-667A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075132 | ||||||
chr16:2075154
|
T | C | 37 | a0001c0001t0016g0295a0001c0002t0002g0282a0001c0002t0006g0017others(34): Show | 41 | HG01070.hp2 HG01884.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.2546-645T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075154 | ||||||
chr16:2075162
|
C | G | 62 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0001g0162others(59): Show | 66 | HG00642.hp1 HG01070.hp2 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.2546-637C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075162 | ||||||
chr16:2075191
|
C | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0132others(1): Show | 4 | HG01074.hp2 HG01934.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546-608C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075191 | ||||||
chr16:2075230
|
A | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0240others(1): Show | 4 | HG00140.hp2 HG01257.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546-569A>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075230 | ||||||
chr16:2075240
|
A | G | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2546-559A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075240 | ||||||
chr16:2075344
|
G | GT | 17 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(14): Show | 19 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.2546-454dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr16 | 2075344 | |||||
chr16:2075354
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2546-445G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075354 | ||||||
chr16:2075400
|
G | A | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2546-399G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075400 | ||||||
chr16:2075489
|
T | C | 38 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0152others(35): Show | 39 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.2546-310T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075489 | ||||||
chr16:2075525
|
C | CA | 30 | a0001c0001t0001g0076a0001c0001t0001g0116a0001c0001t0001g0119others(27): Show | 31 | HG00408.hp1 HG01175.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.2546-249dupA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr16 | 2075525 | |||||
chr16:2075525
|
C | CAAAAA | 13 | a0001c0001t0001g0093a0001c0001t0001g0162a0001c0001t0034g0160others(10): Show | 13 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2546-253_2546-249d others(7): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr16 | 2075525 | |||||
chr16:2075525
|
C | CAAAAAAA | 7 | a0001c0001t0001g0152a0001c0001t0001g0183a0001c0001t0001g0212others(4): Show | 8 | HG00642.hp1 HG01099.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.2546-255_2546-249d others(9): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr16 | 2075525 | |||||
chr16:2075525
|
C | CAAAAAAA others(3): Show |
3 | a0006c0013t0010g0137a0006c0013t0010g0139a0008c0028t0010g0138 | 3 | HG02965.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2546-258_2546-249d others(12): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr16 | 2075525 | |||||
chr16:2075525
|
C | CAAAAAAA others(5): Show |
2 | a0001c0032t0001g0121a0001c0050t0035g0298 | 2 | HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2546-260_2546-249d others(14): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr16 | 2075525 | |||||
chr16:2075525
|
CA | C | 12 | a0001c0001t0001g0103a0001c0001t0001g0112a0001c0001t0001g0114others(9): Show | 13 | HG00140.hp1 HG01884.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.2546-249delA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr16 | 2075525 | |||||
chr16:2075628
|
T | C | 3 | a0006c0013t0010g0137a0006c0013t0010g0139a0008c0028t0010g0138 | 3 | HG02965.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2546-171T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075628 | ||||||
chr16:2075768
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0240others(1): Show | 4 | HG00140.hp2 HG01257.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546-31G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075768 | ||||||
chr16:2075787
|
C | T | 63 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0001g0162others(60): Show | 67 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.2546-12C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 22/41 | chr16 | 2075787 | ||||||
chr16:2075927
|
C | G | 1 | a0004c0023t0011g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2639+35C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/41 | chr16 | 2075927 | ||||||
chr16:2075934
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0240 | 2 | HG01257.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2639+42C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/41 | chr16 | 2075934 | ||||||
chr16:2075936
|
C | G | 66 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0001g0162others(63): Show | 70 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.2639+44C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/41 | chr16 | 2075936 | ||||||
chr16:2075994
|
G | A | 1 | a0001c0037t0027g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2640-74G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/41 | chr16 | 2075994 | ||||||
chr16:2075995
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2640-73G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/41 | chr16 | 2075995 | ||||||
chr16:2076003
|
C | T | 1 | a0001c0037t0027g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2640-65C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/41 | chr16 | 2076003 | ||||||
chr16:2076042
|
G | T | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2640-26G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/41 | chr16 | 2076042 | ||||||
chr16:2076055
|
C | T | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2640-13C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 23/41 | chr16 | 2076055 | ||||||
chr16:2076635
|
A | G | 1 | a0001c0053t0001g0169 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2837+50A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2076635 | ||||||
chr16:2076805
|
C | T | 9 | a0001c0001t0016g0295a0001c0002t0016g0128a0001c0004t0005g0012others(6): Show | 11 | HG01884.hp2 HG02300.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2837+220C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2076805 | ||||||
chr16:2076871
|
T | G | 1 | a0001c0002t0006g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2837+286T>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2076871 | ||||||
chr16:2077036
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2837+451C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2077036 | ||||||
chr16:2077040
|
C | CTA | 3 | a0001c0001t0001g0152a0001c0001t0001g0183a0001c0001t0001g0212 | 3 | HG00642.hp1 HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2837+457_2837+458d others(4): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | INFO_REALIGN_3_PRIME | chr16 | 2077040 | |||||
chr16:2077107
|
C | T | 1 | a0001c0001t0003g0216 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2838-491C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2077107 | ||||||
chr16:2077117
|
T | C | 1 | a0001c0001t0024g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2838-481T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2077117 | ||||||
chr16:2077128
|
G | A | 1 | a0015c0040t0033g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2838-470G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2077128 | ||||||
chr16:2077158
|
A | G | 3 | a0006c0013t0010g0137a0006c0013t0010g0139a0008c0028t0010g0138 | 3 | HG02965.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2838-440A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2077158 | ||||||
chr16:2077204
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2838-394G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2077204 | ||||||
chr16:2077226
|
C | T | 9 | a0001c0001t0016g0295a0001c0002t0016g0128a0001c0004t0005g0012others(6): Show | 11 | HG01884.hp2 HG02300.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2838-372C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2077226 | ||||||
chr16:2077316
|
A | C | 32 | a0001c0001t0001g0067a0001c0001t0001g0242a0001c0002t0006g0017others(29): Show | 34 | HG00735.hp2 HG01070.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.2838-282A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 25/41 | chr16 | 2077316 | ||||||
chr16:2077815
|
C | CTCA | 11 | a0001c0009t0014g0008a0001c0009t0014g0141a0001c0050t0035g0298others(8): Show | 12 | HG01070.hp2 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2966+92_2966+94dup others(3): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | INFO_REALIGN_3_PRIME | chr16 | 2077815 | |||||
chr16:2077847
|
C | G | 12 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(9): Show | 12 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2966+121C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2077847 | ||||||
chr16:2077943
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2966+217G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2077943 | ||||||
chr16:2077973
|
G | A | 2 | a0007c0018t0030g0122a0007c0018t0032g0123 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2966+247G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2077973 | ||||||
chr16:2078094
|
A | T | 3 | a0001c0003t0004g0126a0001c0003t0004g0127a0011c0042t0002g0133 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2966+368A>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078094 | ||||||
chr16:2078246
|
C | T | 7 | a0001c0002t0016g0128a0001c0004t0005g0012a0001c0004t0005g0014others(4): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2966+520C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078246 | ||||||
chr16:2078270
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2966+544G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078270 | ||||||
chr16:2078275
|
C | T | 1 | a0001c0008t0009g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2966+549C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078275 | ||||||
chr16:2078592
|
C | T | 1 | a0017c0043t0001g0215 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2967-440C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078592 | ||||||
chr16:2078602
|
C | T | 5 | a0004c0011t0011g0026a0004c0011t0011g0027a0004c0011t0029g0025others(2): Show | 5 | HG01070.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2967-430C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078602 | ||||||
chr16:2078609
|
G | C | 1 | a0001c0001t0001g0219 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2967-423G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078609 | ||||||
chr16:2078613
|
C | G | 47 | a0001c0001t0001g0093a0001c0001t0001g0135a0001c0001t0001g0152others(44): Show | 48 | HG00642.hp1 HG01070.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2967-419C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078613 | ||||||
chr16:2078656
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2967-376C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078656 | ||||||
chr16:2078669
|
C | T | 8 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0036others(5): Show | 8 | HG00280.hp1 HG01074.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2967-363C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078669 | ||||||
chr16:2078692
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2967-340G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078692 | ||||||
chr16:2078728
|
G | A | 2 | a0001c0002t0002g0276a0001c0002t0002g0279 | 2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2967-304G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078728 | ||||||
chr16:2078756
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2967-276T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078756 | ||||||
chr16:2078783
|
C | G | 1 | a0001c0048t0001g0028 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2967-249C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078783 | ||||||
chr16:2078847
|
C | T | 1 | a0001c0037t0027g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2967-185C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078847 | ||||||
chr16:2078848
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2967-184G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078848 | ||||||
chr16:2078867
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2967-165T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078867 | ||||||
chr16:2078914
|
T | C | 15 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(12): Show | 16 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2967-118T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078914 | ||||||
chr16:2078925
|
C | T | 1 | a0001c0032t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2967-107C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 26/41 | chr16 | 2078925 | ||||||
chr16:2079172
|
C | CCAACTTC others(23): Show |
1 | a0018c0033t0001g0110 | 1 | NA18997.hp1 | splice_region_variant&intron_variant | LOW | c.3108_3131+6dupCAAC others(26): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 27/41 | INFO_REALIGN_3_PRIME | chr16 | 2079172 | |||||
chr16:2079246
|
A | G | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3132-30A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 27/41 | chr16 | 2079246 | ||||||
chr16:2079260
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3132-16G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 27/41 | chr16 | 2079260 | ||||||
chr16:2079489
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3284+61G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 28/41 | chr16 | 2079489 | ||||||
chr16:2079494
|
A | G | 1 | a0022c0025t0001g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3285-63A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 28/41 | chr16 | 2079494 | ||||||
chr16:2079725
|
C | T | 2 | a0007c0018t0030g0122a0007c0018t0032g0123 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3397+56C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 29/41 | chr16 | 2079725 | ||||||
chr16:2079768
|
T | A | 1 | a0001c0051t0003g0233 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3397+99T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 29/41 | chr16 | 2079768 | ||||||
chr16:2079784
|
C | T | 1 | a0001c0001t0015g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3397+115C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 29/41 | chr16 | 2079784 | ||||||
chr16:2079795
|
C | T | 10 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(7): Show | 10 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3397+126C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 29/41 | chr16 | 2079795 | ||||||
chr16:2079830
|
G | A | 3 | a0007c0018t0030g0122a0007c0018t0032g0123a0012c0045t0025g0299 | 3 | HG02257.hp1 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3397+161G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 29/41 | chr16 | 2079830 | ||||||
chr16:2079900
|
G | A | 3 | a0001c0012t0001g0073a0001c0012t0001g0080a0001c0012t0001g0131 | 3 | HG02486.hp1 HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3397+231G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 29/41 | chr16 | 2079900 | ||||||
chr16:2079953
|
G | C | 1 | a0014c0029t0031g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3398-212G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 29/41 | chr16 | 2079953 | ||||||
chr16:2080025
|
C | T | 8 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0040others(5): Show | 8 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3398-140C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 29/41 | chr16 | 2080025 | ||||||
chr16:2080418
|
T | TC | 21 | a0001c0002t0002g0276a0001c0002t0002g0279a0001c0002t0002g0280others(18): Show | 21 | HG01070.hp2 HG01243.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3610+42dupC | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | INFO_REALIGN_3_PRIME | chr16 | 2080418 | |||||
chr16:2080448
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3610+71G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080448 | ||||||
chr16:2080491
|
G | GT | 36 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0152others(33): Show | 38 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.3610+124dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | INFO_REALIGN_3_PRIME | chr16 | 2080491 | |||||
chr16:2080545
|
G | A | 10 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(7): Show | 10 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3610+168G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080545 | ||||||
chr16:2080547
|
A | C | 10 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(7): Show | 10 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3610+170A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080547 | ||||||
chr16:2080548
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0162a0001c0001t0034g0160others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3610+171A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080548 | ||||||
chr16:2080576
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3610+199C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080576 | ||||||
chr16:2080603
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0240others(1): Show | 4 | HG00140.hp2 HG01257.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3610+226C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080603 | ||||||
chr16:2080622
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0171 | 2 | NA18961.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.3610+245C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080622 | ||||||
chr16:2080632
|
C | T | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3610+255C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080632 | ||||||
chr16:2080633
|
G | A | 1 | a0001c0002t0002g0289 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3610+256G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080633 | ||||||
chr16:2080639
|
A | G | 8 | a0001c0004t0005g0012a0001c0004t0005g0014a0001c0004t0005g0140others(5): Show | 10 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3610+262A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080639 | ||||||
chr16:2080675
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3610+298G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080675 | ||||||
chr16:2080685
|
T | C | 17 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0157others(14): Show | 17 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.3610+308T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080685 | ||||||
chr16:2080686
|
G | A | 1 | a0001c0001t0015g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3610+309G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080686 | ||||||
chr16:2080689
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3610+312T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080689 | ||||||
chr16:2080691
|
A | G | 2 | a0001c0001t0003g0216a0001c0001t0019g0241 | 2 | HG03669.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.3610+314A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080691 | ||||||
chr16:2080693
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0134a0001c0001t0003g0232others(1): Show | 4 | HG00099.hp2 HG01975.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.3610+316C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080693 | ||||||
chr16:2080694
|
C | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0271 | 2 | NA18945.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.3610+317C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080694 | ||||||
chr16:2080696
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3610+319G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080696 | ||||||
chr16:2080698
|
A | G | 1 | a0001c0002t0002g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3610+321A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080698 | ||||||
chr16:2080706
|
A | C | 13 | a0001c0001t0001g0248a0001c0001t0001g0294a0001c0001t0013g0220others(10): Show | 15 | HG01081.hp2 HG01109.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.3610+329A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080706 | ||||||
chr16:2080706
|
A | G | 9 | a0001c0001t0001g0136a0001c0001t0001g0166a0001c0001t0001g0167others(6): Show | 9 | HG01515.hp2 HG01517.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3610+329A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080706 | ||||||
chr16:2080720
|
G | A | 1 | a0018c0033t0001g0110 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.3610+343G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080720 | ||||||
chr16:2080726
|
C | T | 90 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0001g0162others(87): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.3610+349C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080726 | ||||||
chr16:2080727
|
G | A | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3610+350G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080727 | ||||||
chr16:2080735
|
T | C | 6 | a0001c0002t0002g0006a0001c0002t0002g0020a0001c0002t0002g0060others(3): Show | 7 | HG01884.hp1 HG02055.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3610+358T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080735 | ||||||
chr16:2080737
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3610+360G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080737 | ||||||
chr16:2080752
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3610+375G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080752 | ||||||
chr16:2080771
|
A | C | 1 | a0011c0042t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3610+394A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080771 | ||||||
chr16:2080774
|
G | A | 23 | a0001c0001t0001g0084a0001c0001t0001g0093a0001c0001t0001g0152others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.3610+397G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080774 | ||||||
chr16:2080775
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0086others(6): Show | 10 | HG01074.hp2 HG01934.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.3610+398C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080775 | ||||||
chr16:2080777
|
C | T | 1 | a0001c0001t0038g0177 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3610+400C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080777 | ||||||
chr16:2080780
|
A | G | 18 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0086others(15): Show | 19 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3610+403A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080780 | ||||||
chr16:2080808
|
C | T | 34 | a0001c0001t0001g0084a0001c0001t0001g0093a0001c0001t0001g0152others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.3610+431C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080808 | ||||||
chr16:2080896
|
C | T | 2 | a0001c0009t0014g0008a0001c0009t0014g0141 | 3 | HG02723.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3610+519C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2080896 | ||||||
chr16:2081177
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3611-418G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2081177 | ||||||
chr16:2081215
|
C | CGCAGAGG others(30): Show |
2 | a0001c0007t0002g0041a0001c0007t0002g0042 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3611-358_3611-322d others(39): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | INFO_REALIGN_3_PRIME | chr16 | 2081215 | |||||
chr16:2081236
|
G | A | 1 | a0001c0001t0020g0170 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3611-359G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2081236 | ||||||
chr16:2081275
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0230 | 2 | NA18970.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.3611-320C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2081275 | ||||||
chr16:2081288
|
C | T | 63 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0001g0162others(60): Show | 67 | HG00642.hp1 HG01069.hp2 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.3611-307C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2081288 | ||||||
chr16:2081525
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3611-70G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2081525 | ||||||
chr16:2081536
|
G | A | 2 | a0007c0018t0030g0122a0007c0018t0032g0123 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3611-59G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 30/41 | chr16 | 2081536 | ||||||
chr16:2081854
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3814+56C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2081854 | ||||||
chr16:2081939
|
C | T | 8 | a0001c0001t0001g0093a0001c0001t0001g0152a0001c0001t0001g0162others(5): Show | 8 | HG00642.hp1 HG01099.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.3814+141C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2081939 | ||||||
chr16:2081963
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3814+165G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2081963 | ||||||
chr16:2081992
|
T | A | 4 | a0001c0001t0001g0181a0001c0001t0001g0214a0001c0001t0001g0259others(1): Show | 4 | HG00280.hp2 HG02074.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3814+194T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2081992 | ||||||
chr16:2082051
|
G | T | 1 | a0003c0006t0002g0291 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3814+253G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2082051 | ||||||
chr16:2082069
|
C | T | 1 | a0001c0002t0007g0228 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3814+271C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2082069 | ||||||
chr16:2082087
|
G | C | 3 | a0001c0001t0001g0154a0001c0001t0001g0195a0001c0001t0001g0230 | 3 | NA18970.hp2 NA18974.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3814+289G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2082087 | ||||||
chr16:2082099
|
C | CT | 15 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(12): Show | 16 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.3814+302dupT | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr16 | 2082099 | |||||
chr16:2082281
|
A | G | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0193 | 3 | HG01106.hp2 HG01433.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.3815-155A>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2082281 | ||||||
chr16:2082313
|
G | A | 1 | a0001c0003t0004g0297 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3815-123G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2082313 | ||||||
chr16:2082378
|
C | T | 3 | a0001c0007t0012g0005a0001c0007t0012g0022a0001c0007t0012g0023 | 4 | HG01891.hp1 HG02896.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3815-58C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2082378 | ||||||
chr16:2082416
|
C | T | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3815-20C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 31/41 | chr16 | 2082416 | ||||||
chr16:2082512
|
C | G | 5 | a0001c0007t0002g0041a0001c0007t0002g0042a0001c0007t0012g0005others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.3883+8C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082512 | ||||||
chr16:2082541
|
C | T | 1 | a0001c0001t0003g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3883+37C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082541 | ||||||
chr16:2082570
|
G | A | 5 | a0001c0007t0002g0041a0001c0007t0002g0042a0001c0007t0012g0005others(2): Show | 6 | HG01891.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3883+66G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082570 | ||||||
chr16:2082582
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3883+78G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082582 | ||||||
chr16:2082605
|
C | T | 1 | a0001c0014t0009g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3883+101C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082605 | ||||||
chr16:2082649
|
T | C | 1 | a0001c0015t0005g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3883+145T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082649 | ||||||
chr16:2082730
|
G | A | 49 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0001t0016g0295others(46): Show | 51 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.3883+226G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082730 | ||||||
chr16:2082739
|
C | T | 1 | a0001c0037t0027g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3883+235C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082739 | ||||||
chr16:2082833
|
G | A | 1 | a0001c0001t0023g0081 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3883+329G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082833 | ||||||
chr16:2082973
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3883+469C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2082973 | ||||||
chr16:2083032
|
G | A | 1 | a0001c0001t0024g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3883+528G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2083032 | ||||||
chr16:2083086
|
C | G | 1 | a0001c0048t0001g0028 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3883+582C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2083086 | ||||||
chr16:2083114
|
C | T | 1 | a0001c0001t0019g0241 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3884-581C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2083114 | ||||||
chr16:2083177
|
C | A | 2 | a0007c0018t0030g0122a0007c0018t0032g0123 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3884-518C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2083177 | ||||||
chr16:2083235
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3884-460G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2083235 | ||||||
chr16:2083332
|
C | T | 12 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(9): Show | 12 | HG02109.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3884-363C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2083332 | ||||||
chr16:2083578
|
G | A | 4 | a0002c0005t0001g0078a0002c0005t0001g0087a0002c0005t0001g0089others(1): Show | 4 | NA18960.hp1 NA18966.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.3884-117G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2083578 | ||||||
chr16:2083627
|
C | T | 1 | a0001c0037t0027g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3884-68C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2083627 | ||||||
chr16:2083639
|
C | G | 7 | a0001c0008t0009g0029a0001c0008t0009g0030a0001c0008t0009g0033others(4): Show | 7 | HG00639.hp2 HG00741.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.3884-56C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 32/41 | chr16 | 2083639 | ||||||
chr16:2083900
|
C | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0112a0001c0001t0001g0116others(13): Show | 16 | HG00558.hp1 HG00733.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.4005+84C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2083900 | ||||||
chr16:2083969
|
T | A | 8 | a0004c0011t0011g0026a0004c0011t0011g0027a0004c0011t0029g0025others(5): Show | 8 | HG01070.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4005+153T>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2083969 | ||||||
chr16:2083973
|
G | T | 1 | a0001c0007t0012g0022 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4005+157G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2083973 | ||||||
chr16:2084032
|
A | C | 1 | a0001c0052t0001g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4006-196A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2084032 | ||||||
chr16:2084086
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4006-142G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2084086 | ||||||
chr16:2084088
|
C | T | 2 | a0001c0017t0001g0208a0001c0017t0001g0293 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4006-140C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2084088 | ||||||
chr16:2084109
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.4006-119C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2084109 | ||||||
chr16:2084134
|
G | A | 4 | a0006c0013t0010g0137a0006c0013t0010g0139a0008c0028t0010g0138others(1): Show | 4 | HG02615.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4006-94G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2084134 | ||||||
chr16:2084195
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4006-33G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2084195 | ||||||
chr16:2084205
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4006-23C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 33/41 | chr16 | 2084205 | ||||||
chr16:2084733
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4493+18G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 34/41 | chr16 | 2084733 | ||||||
chr16:2084851
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4494-100G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 34/41 | chr16 | 2084851 | ||||||
chr16:2085070
|
C | T | 4 | a0007c0018t0030g0122a0007c0018t0032g0123a0012c0045t0025g0299others(1): Show | 4 | HG02257.hp1 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4569+44C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 35/41 | chr16 | 2085070 | ||||||
chr16:2085073
|
G | A | 9 | a0001c0001t0001g0135a0001c0001t0016g0295a0001c0002t0016g0128others(6): Show | 10 | HG02300.hp2 HG02717.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.4569+47G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 35/41 | chr16 | 2085073 | ||||||
chr16:2085527
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.4662+205C>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/41 | chr16 | 2085527 | ||||||
chr16:2085568
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4662+246C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/41 | chr16 | 2085568 | ||||||
chr16:2085638
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.4662+316G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/41 | chr16 | 2085638 | ||||||
chr16:2085687
|
G | A | 1 | a0001c0001t0010g0156 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4662+365G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/41 | chr16 | 2085687 | ||||||
chr16:2085724
|
G | A | 1 | a0001c0004t0005g0281 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4662+402G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/41 | chr16 | 2085724 | ||||||
chr16:2085757
|
C | T | 1 | a0001c0001t0024g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4662+435C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/41 | chr16 | 2085757 | ||||||
chr16:2085818
|
G | C | 17 | a0001c0001t0016g0295a0001c0002t0016g0128a0001c0009t0014g0008others(14): Show | 18 | HG01070.hp2 HG02257.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.4663-375G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/41 | chr16 | 2085818 | ||||||
chr16:2085867
|
T | C | 4 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0261others(1): Show | 4 | HG03710.hp2 HG03831.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.4663-326T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/41 | chr16 | 2085867 | ||||||
chr16:2086105
|
C | T | 6 | a0001c0001t0016g0295a0001c0009t0014g0008a0001c0009t0014g0141others(3): Show | 7 | HG02300.hp2 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.4663-88C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 36/41 | chr16 | 2086105 | ||||||
chr16:2086454
|
C | T | 10 | a0001c0001t0001g0067a0001c0001t0001g0092a0001c0001t0001g0172others(7): Show | 10 | HG00099.hp2 HG00408.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.4849+75C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 37/41 | chr16 | 2086454 | ||||||
chr16:2086455
|
G | A | 5 | a0004c0023t0011g0164a0007c0018t0030g0122a0007c0018t0032g0123others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.4849+76G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 37/41 | chr16 | 2086455 | ||||||
chr16:2086475
|
CA | C | 11 | a0001c0002t0006g0017a0001c0002t0006g0021a0001c0002t0006g0035others(8): Show | 11 | HG02280.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.4849+97delA | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 37/41 | chr16 | 2086475 | ||||||
chr16:2086517
|
C | G | 1 | a0001c0001t0024g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4849+138C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 37/41 | chr16 | 2086517 | ||||||
chr16:2086623
|
T | C | 66 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0001t0016g0295others(63): Show | 70 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.4850-109T>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 37/41 | chr16 | 2086623 | ||||||
chr16:2086635
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.4850-97C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 37/41 | chr16 | 2086635 | ||||||
chr16:2086886
|
G | A | 3 | a0006c0013t0010g0137a0006c0013t0010g0139a0008c0028t0010g0138 | 3 | HG02965.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4989+15G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2086886 | ||||||
chr16:2086961
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4989+90C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2086961 | ||||||
chr16:2086978
|
A | C | 12 | a0001c0003t0004g0126a0001c0003t0004g0127a0001c0003t0004g0142others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.4989+107A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2086978 | ||||||
chr16:2087013
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4989+142G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087013 | ||||||
chr16:2087115
|
G | C | 1 | a0001c0002t0016g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4989+244G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087115 | ||||||
chr16:2087277
|
G | A | 1 | a0001c0002t0016g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4989+406G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087277 | ||||||
chr16:2087292
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.4989+421C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087292 | ||||||
chr16:2087297
|
C | T | 1 | a0001c0002t0002g0061 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4989+426C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087297 | ||||||
chr16:2087485
|
T | TG | 38 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0066others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.4990-365dupG | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | INFO_REALIGN_3_PRIME | chr16 | 2087485 | |||||
chr16:2087485
|
TGGG | T | 59 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0036others(56): Show | 62 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.4990-367_4990-365d others(5): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | INFO_REALIGN_3_PRIME | chr16 | 2087485 | |||||
chr16:2087489
|
G | T | 1 | a0001c0001t0016g0295 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4990-374G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087489 | ||||||
chr16:2087490
|
G | T | 3 | a0001c0009t0014g0008a0001c0009t0014g0141a0001c0037t0027g0059 | 4 | HG02723.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4990-373G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087490 | ||||||
chr16:2087569
|
C | T | 1 | a0001c0001t0013g0220 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4990-294C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087569 | ||||||
chr16:2087725
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4990-138C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087725 | ||||||
chr16:2087804
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4990-59C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087804 | ||||||
chr16:2087805
|
G | A | 8 | a0004c0011t0011g0026a0004c0011t0011g0027a0004c0011t0029g0025others(5): Show | 8 | HG01070.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4990-58G>A | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087805 | ||||||
chr16:2087810
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4990-53C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087810 | ||||||
chr16:2087856
|
C | T | 4 | a0001c0001t0016g0295a0001c0009t0014g0008a0001c0009t0014g0141others(1): Show | 5 | HG02300.hp2 HG02723.hp2 HG02970.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.4990-7C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 38/41 | chr16 | 2087856 | ||||||
chr16:2087923
|
T | TCCCTGCA others(27): Show |
2 | a0013c0035t0011g0024a0015c0040t0033g0267 | 2 | HG01070.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.5068+27_5069-47dup others(34): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr16 | 2087923 | |||||
chr16:2087923
|
TCCCTGCA others(27): Show |
T | 1 | a0016c0038t0003g0100 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.5068+27_5069-47del others(34): Show |
TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 39/41 | INFO_REALIGN_3_PRIME | chr16 | 2087923 | |||||
chr16:2088217
|
A | C | 72 | a0001c0001t0001g0152a0001c0001t0002g0038a0001c0001t0002g0047others(69): Show | 77 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.5161-10A>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 40/41 | chr16 | 2088217 | ||||||
chr16:2088349
|
G | C | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.5259+24G>C | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 41/41 | chr16 | 2088349 | ||||||
chr16:2088397
|
C | T | 48 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0006others(45): Show | 51 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.5260-49C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 41/41 | chr16 | 2088397 | ||||||
chr16:2088421
|
C | G | 61 | a0001c0001t0002g0038a0001c0001t0002g0047a0001c0002t0002g0006others(58): Show | 65 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.5260-25C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 41/41 | chr16 | 2088421 | ||||||
chr16:2088431
|
C | T | 1 | a0001c0037t0027g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5260-15C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 41/41 | chr16 | 2088431 |