Item | Value |
---|---|
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 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0002 | 0/0 | 1807 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0003 | 0/0 | 1807 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0004 | 0/0 | 1807 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0005 | 0/0 | 1807 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0006 | 0/0 | 1807 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0007 | 0/0 | 1807 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0008 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0009 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0010 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0011 | 0/0 | 1801 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1796): Show |
chr16 | 2042985 | 2094491 |
a0012 | 0/0 | 1715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1710): Show |
chr16 | 2042985 | 2094491 |
a0013 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1710): Show |
chr16 | 2042985 | 2094491 |
a0014 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0015 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0016 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0017 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0018 | 0/0 | 1807 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0019 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0020 | 0/0 | 1807 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0021 | 0/0 | 1807 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0022 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
a0023 | 0/0 | 1817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1812): Show |
chr16 | 2042985 | 2094491 |
a0024 | 0/0 | 1807 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | MAKPT others(1802): Show |
chr16 | 2042985 | 2094491 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5421 | 179 | 17 | 53 | 68 | 8 | 32 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0002 | 0/1 | 5421 | 31 | 22 | 7 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0003 | 0/0 | 5421 | 13 | 11 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0004 | 0/0 | 5421 | 8 | 8 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0007 | 0/0 | 5421 | 6 | 6 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0008 | 0/0 | 5421 | 4 | 0 | 2 | 0 | 1 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0009 | 0/0 | 5421 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0012 | 0/0 | 5421 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0014 | 0/0 | 5421 | 2 | 0 | 1 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0015 | 0/0 | 5421 | 2 | 1 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0016 | 0/0 | 5421 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0017 | 0/0 | 5421 | 2 | 0 | 0 | 0 | 0 | 2 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0019 | 0/0 | 5421 | 2 | 0 | 1 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0020 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0021 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0022 | 0/0 | 5421 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0024 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0032 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0034 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0036 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0037 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0039 | 0/0 | 5421 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0041 | 0/0 | 5421 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0046 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0047 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0048 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0049 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0050 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0051 | 0/0 | 5421 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0052 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0001c0053 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0002c0005 | 0/0 | 5421 | 8 | 0 | 0 | 8 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0003c0006 | 0/0 | 5421 | 7 | 6 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0004c0011 | 0/0 | 5421 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0004c0023 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0005c0010 | 0/0 | 5421 | 3 | 0 | 0 | 0 | 2 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0006c0018 | 0/0 | 5421 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0007c0013 | 0/0 | 5421 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0008c0026 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0009c0055 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0010c0031 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0011c0038 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5398): Show |
chr16 | 2042985 | 2094491 | ||
a0012c0035 | 0/0 | 5455 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5450): Show |
chr16 | 2042985 | 2094491 | ||
a0013c0040 | 0/0 | 5455 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5450): Show |
chr16 | 2042985 | 2094491 | ||
a0014c0043 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0015c0042 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0016c0029 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0017c0045 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0018c0044 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0019c0028 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0020c0054 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0021c0027 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0022c0025 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
chr16 | 2042985 | 2094491 | ||
a0023c0033 | 0/0 | 5451 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5446): Show |
chr16 | 2042985 | 2094491 | ||
a0024c0030 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | ATGGC others(5416): Show |
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 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0002 | 0/0 | 6421 | 2 | 0 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6416): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0003 | 0/0 | 6417 | 23 | 0 | 11 | 11 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6412): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0007 | 0/0 | 6415 | 4 | 0 | 0 | 0 | 0 | 4 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0008 | 0/0 | 6409 | 6 | 0 | 1 | 0 | 0 | 5 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6404): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0010 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0013 | 0/0 | 6419 | 3 | 0 | 0 | 3 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6414): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0015 | 0/0 | 6417 | 2 | 0 | 0 | 1 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6412): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0016 | 0/0 | 6413 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6408): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0017 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6412): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0019 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6398): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0020 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0021 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0022 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0023 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0024 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0026 | 0/0 | 6413 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6408): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0028 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6404): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0034 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0001t0038 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0002t0002 | 0/1 | 6421 | 17 | 13 | 3 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6416): Show |
chr16 | 2042985 | 2094491 |
a0001c0002t0005 | 0/0 | 6423 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6418): Show |
chr16 | 2042985 | 2094491 |
a0001c0002t0006 | 0/0 | 6421 | 7 | 7 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6416): Show |
chr16 | 2042985 | 2094491 |
a0001c0002t0007 | 0/0 | 6415 | 4 | 0 | 3 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0002t0016 | 0/0 | 6413 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6408): Show |
chr16 | 2042985 | 2094491 |
a0001c0002t0018 | 0/0 | 6423 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6418): Show |
chr16 | 2042985 | 2094491 |
a0001c0003t0004 | 0/0 | 6411 | 12 | 10 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6406): Show |
chr16 | 2042985 | 2094491 |
a0001c0003t0010 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0004t0005 | 0/0 | 6423 | 8 | 8 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6418): Show |
chr16 | 2042985 | 2094491 |
a0001c0007t0002 | 0/0 | 6421 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6416): Show |
chr16 | 2042985 | 2094491 |
a0001c0007t0012 | 0/0 | 6415 | 4 | 4 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0008t0009 | 0/0 | 6411 | 4 | 0 | 2 | 0 | 1 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6406): Show |
chr16 | 2042985 | 2094491 |
a0001c0009t0014 | 0/0 | 6413 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6408): Show |
chr16 | 2042985 | 2094491 |
a0001c0012t0001 | 0/0 | 6415 | 3 | 3 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0014t0009 | 0/0 | 6411 | 2 | 0 | 1 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6406): Show |
chr16 | 2042985 | 2094491 |
a0001c0015t0005 | 0/0 | 6423 | 2 | 1 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6418): Show |
chr16 | 2042985 | 2094491 |
a0001c0016t0001 | 0/0 | 6415 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0017t0001 | 0/0 | 6415 | 2 | 0 | 0 | 0 | 0 | 2 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0019t0002 | 0/0 | 6421 | 2 | 0 | 1 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6416): Show |
chr16 | 2042985 | 2094491 |
a0001c0020t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0021t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0022t0001 | 0/0 | 6415 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0024t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0032t0001 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0034t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0036t0006 | 0/0 | 6421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6416): Show |
chr16 | 2042985 | 2094491 |
a0001c0037t0027 | 0/0 | 6413 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6408): Show |
chr16 | 2042985 | 2094491 |
a0001c0039t0001 | 0/0 | 6415 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0041t0001 | 0/0 | 6415 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0046t0006 | 0/0 | 6421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6416): Show |
chr16 | 2042985 | 2094491 |
a0001c0047t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0048t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0049t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0050t0035 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0051t0003 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6412): Show |
chr16 | 2042985 | 2094491 |
a0001c0052t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0001c0053t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0002c0005t0001 | 0/0 | 6415 | 7 | 0 | 0 | 7 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0002c0005t0003 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6412): Show |
chr16 | 2042985 | 2094491 |
a0003c0006t0002 | 0/0 | 6421 | 5 | 4 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6416): Show |
chr16 | 2042985 | 2094491 |
a0003c0006t0036 | 0/0 | 6425 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6420): Show |
chr16 | 2042985 | 2094491 |
a0003c0006t0037 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0004c0011t0011 | 0/0 | 6417 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6412): Show |
chr16 | 2042985 | 2094491 |
a0004c0011t0029 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0004c0023t0011 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6412): Show |
chr16 | 2042985 | 2094491 |
a0005c0010t0001 | 0/0 | 6415 | 3 | 0 | 0 | 0 | 2 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0006c0018t0030 | 0/0 | 6431 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6426): Show |
chr16 | 2042985 | 2094491 |
a0006c0018t0032 | 0/0 | 6439 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6434): Show |
chr16 | 2042985 | 2094491 |
a0007c0013t0010 | 0/0 | 6415 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0008c0026t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0009c0055t0003 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6412): Show |
chr16 | 2042985 | 2094491 |
a0010c0031t0015 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6412): Show |
chr16 | 2042985 | 2094491 |
a0011c0038t0003 | 0/0 | 6399 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6394): Show |
chr16 | 2042985 | 2094491 |
a0012c0035t0011 | 0/0 | 6451 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6446): Show |
chr16 | 2042985 | 2094491 |
a0013c0040t0033 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6444): Show |
chr16 | 2042985 | 2094491 |
a0014c0043t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0015c0042t0002 | 0/0 | 6421 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6416): Show |
chr16 | 2042985 | 2094491 |
a0016c0029t0031 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6424): Show |
chr16 | 2042985 | 2094491 |
a0017c0045t0025 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0018c0044t0008 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6404): Show |
chr16 | 2042985 | 2094491 |
a0019c0028t0010 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0020c0054t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0021c0027t0001 | 0/0 | 6415 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0022c0025t0001 | 0/0 | 6415 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
chr16 | 2042985 | 2094491 |
a0023c0033t0001 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6440): Show |
chr16 | 2042985 | 2094491 |
a0024c0030t0001 | 0/0 | 6415 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | GCTTC others(6410): Show |
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 |
a0001c0001t0001g0008 | 1/0 | 1 | 0 | 0 | 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 | 2 | 0 | 2 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
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 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0170 | 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 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0187 | 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 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0198 | 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 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0264 | 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 |
a0001c0001t0001g0267 | 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 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0002g0046 | 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 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0234 | 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 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0010g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0013g0219 | 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 |
a0001c0001t0013g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0015g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0015g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0016g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0017g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0019g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0020g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0021g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0022g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0023g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0024g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0026g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0001t0028g0054 | 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 |
a0001c0001t0038g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0278 | 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 |
a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0002t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0006g0041 | 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 |
a0001c0002t0006g0047 | 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 |
a0001c0002t0007g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0016g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0002t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0125 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0003t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0003t0004g0145 | 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 |
a0001c0003t0004g0295 | 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 |
a0001c0003t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0004t0005g0285 | 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 |
a0001c0007t0002g0043 | 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 |
a0001c0007t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0007t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0008t0009g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0008t0009g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0008t0009g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0008t0009g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0009t0014g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0009t0014g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0012t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0012t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0012t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0014t0009g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0014t0009g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0015t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0015t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0016t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0016t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0017t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0017t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0019t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0019t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0020t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0021t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0022t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0024t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0032t0001g0120 | 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 |
a0001c0036t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0037t0027g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0039t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0041t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0046t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0047t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0048t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0049t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0050t0035g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0051t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0052t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0001c0053t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0086 | 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 |
a0002c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0002c0005t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0036g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0003c0006t0037g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0004c0011t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0004c0011t0011g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0004c0011t0029g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0004c0023t0011g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0005c0010t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0006c0018t0030g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0006c0018t0032g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0007c0013t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0007c0013t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0008c0026t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0009c0055t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0010c0031t0015g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0011c0038t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0012c0035t0011g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0013c0040t0033g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0014c0043t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0015c0042t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0016c0029t0031g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0017c0045t0025g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0018c0044t0008g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0019c0028t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0020c0054t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0021c0027t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0022c0025t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0023c0033t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
a0024c0030t0001g0072 | 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 | g0176 | EUR | GBR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00099 | hp2 | a0001 | c0052 | t0001 | g0016 | EUR | GBR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00140 | hp2 | a0001 | c0049 | t0001 | g0032 | EUR | GBR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00280 | hp1 | a0001 | c0019 | t0002 | g0038 | EUR | FIN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | FIN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00408 | hp2 | a0008 | c0026 | t0001 | g0172 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00438 | hp1 | a0009 | c0055 | t0003 | g0186 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0195 | 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 | g0197 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00558 | hp1 | a0001 | c0001 | t0017 | g0175 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00609 | hp2 | a0001 | c0001 | t0022 | g0164 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00621 | hp1 | a0010 | c0031 | t0015 | g0004 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0287 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00639 | hp2 | a0001 | c0008 | t0009 | g0031 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0182 | 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 | g0254 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00733 | hp2 | a0011 | c0038 | t0003 | g0098 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00741 | hp1 | a0001 | c0001 | t0008 | g0095 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG00741 | hp2 | a0001 | c0014 | t0009 | g0048 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01069 | hp2 | a0001 | c0003 | t0004 | g0125 | 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 | a0012 | c0035 | t0011 | g0026 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01071 | hp1 | a0001 | c0003 | t0004 | g0126 | 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 | g0046 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01081 | hp1 | a0001 | c0002 | t0005 | g0049 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01106 | hp1 | a0001 | c0039 | t0001 | g0184 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01109 | hp1 | a0001 | c0041 | t0001 | g0228 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01109 | hp2 | a0001 | c0015 | t0005 | g0277 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01192 | hp2 | a0001 | c0022 | t0001 | g0108 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | PUR | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01243 | hp2 | a0003 | c0006 | t0002 | g0284 | 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 | g0187 | 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 | g0234 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0178 | 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 | g0227 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01346 | hp1 | a0001 | c0008 | t0009 | g0063 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0037 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01496 | hp2 | a0001 | c0019 | t0002 | g0051 | AMR | CLM | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01516 | hp1 | a0005 | c0010 | t0001 | g0243 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01517 | hp1 | a0005 | c0010 | t0001 | g0242 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01884 | hp2 | a0001 | c0004 | t0005 | g0013 | 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 | a0013 | c0040 | t0033 | g0266 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01928 | hp1 | a0001 | c0051 | t0003 | g0232 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01928 | hp2 | a0001 | c0001 | t0026 | g0012 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0039 | 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 | g0011 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0237 | 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 | g0217 | 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 | g0205 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0056 | 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 | g0102 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02015 | hp1 | a0001 | c0047 | t0001 | g0077 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02015 | hp2 | a0002 | c0005 | t0001 | g0068 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02040 | hp2 | a0001 | c0001 | t0013 | g0219 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0060 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02080 | hp2 | a0014 | c0043 | t0001 | g0214 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0278 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02145 | hp2 | a0001 | c0016 | t0001 | g0274 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02155 | hp1 | a0001 | c0001 | t0013 | g0259 | EAS | CDX | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02155 | hp2 | a0001 | c0001 | t0020 | g0169 | EAS | CDX | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02257 | hp1 | a0006 | c0018 | t0030 | g0121 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0288 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02258 | hp2 | a0004 | c0023 | t0011 | g0156 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02280 | hp1 | a0003 | c0006 | t0036 | g0014 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02280 | hp2 | a0001 | c0002 | t0006 | g0018 | 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 | g0294 | AMR | PEL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02451 | hp1 | a0001 | c0001 | t0024 | g0017 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02451 | hp2 | a0001 | c0004 | t0005 | g0139 | 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 | g0220 | EAS | KHV | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02572 | hp1 | a0003 | c0006 | t0002 | g0283 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02602 | hp1 | a0005 | c0010 | t0001 | g0244 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02615 | hp1 | a0001 | c0016 | t0001 | g0094 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02615 | hp2 | a0015 | c0042 | t0002 | g0132 | 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 | g0141 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02630 | hp1 | a0001 | c0004 | t0005 | g0285 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02630 | hp2 | a0001 | c0002 | t0006 | g0041 | 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 | g0130 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02717 | hp2 | a0001 | c0003 | t0004 | g0145 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0036 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02723 | hp2 | a0001 | c0009 | t0014 | g0140 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02735 | hp2 | a0001 | c0014 | t0009 | g0193 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02809 | hp2 | a0004 | c0011 | t0029 | g0027 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02818 | hp1 | a0001 | c0003 | t0004 | g0147 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02818 | hp2 | a0001 | c0004 | t0005 | g0280 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02886 | hp1 | a0001 | c0012 | t0001 | g0078 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0281 | 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 | g0007 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02896 | hp1 | a0001 | c0003 | t0004 | g0149 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02896 | hp2 | a0001 | c0007 | t0012 | g0023 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02897 | hp1 | a0001 | c0003 | t0004 | g0148 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0059 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02922 | hp1 | a0001 | c0007 | t0002 | g0042 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02922 | hp2 | a0001 | c0004 | t0005 | g0015 | 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 | a0007 | c0013 | t0010 | g0138 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02970 | hp1 | a0001 | c0009 | t0014 | g0009 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02970 | hp2 | a0003 | c0006 | t0002 | g0286 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03041 | hp1 | a0001 | c0004 | t0005 | g0282 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03041 | hp2 | a0001 | c0050 | t0035 | g0297 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03098 | hp2 | a0016 | c0029 | t0031 | g0035 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03130 | hp1 | a0006 | c0018 | t0032 | g0122 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03130 | hp2 | a0003 | c0006 | t0002 | g0290 | 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 | a0007 | c0013 | t0010 | g0136 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03195 | hp1 | a0001 | c0002 | t0006 | g0022 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0289 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03209 | hp2 | a0017 | c0045 | t0025 | g0298 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03225 | hp1 | a0001 | c0007 | t0002 | g0043 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03225 | hp2 | a0004 | c0011 | t0011 | g0025 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03239 | hp1 | a0018 | c0044 | t0008 | g0096 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03239 | hp2 | a0001 | c0001 | t0008 | g0123 | 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 | a0019 | c0028 | t0010 | g0137 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03486 | hp1 | a0001 | c0009 | t0014 | g0009 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03486 | hp2 | a0003 | c0006 | t0002 | g0014 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03491 | hp1 | a0001 | c0017 | t0001 | g0292 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03491 | hp2 | a0001 | c0001 | t0008 | g0154 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03492 | hp1 | a0001 | c0017 | t0001 | g0207 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0256 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03516 | hp2 | a0001 | c0002 | t0016 | g0127 | AFR | ESN | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03540 | hp1 | a0001 | c0007 | t0012 | g0024 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03540 | hp2 | a0001 | c0003 | t0004 | g0146 | AFR | GWD | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03579 | hp1 | a0003 | c0006 | t0037 | g0273 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03579 | hp2 | a0001 | c0003 | t0004 | g0143 | AFR | MSL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03654 | hp2 | a0020 | c0054 | t0001 | g0112 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03669 | hp2 | a0001 | c0001 | t0019 | g0240 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0252 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03704 | hp1 | a0001 | c0001 | t0015 | g0238 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03704 | hp2 | a0001 | c0001 | t0008 | g0070 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03710 | hp1 | a0001 | c0008 | t0009 | g0034 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0221 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03942 | hp1 | a0021 | c0027 | t0001 | g0020 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03942 | hp2 | a0001 | c0001 | t0008 | g0263 | SAS | BEB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04115 | hp2 | a0001 | c0048 | t0001 | g0029 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04199 | hp2 | a0001 | c0001 | t0007 | g0250 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04204 | hp1 | a0001 | c0053 | t0001 | g0168 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG04228 | hp1 | a0001 | c0001 | t0007 | g0225 | 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 | g0142 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18522 | hp2 | a0001 | c0003 | t0004 | g0296 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18612 | hp1 | a0002 | c0005 | t0001 | g0086 | EAS | CHB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18906 | hp1 | a0001 | c0004 | t0005 | g0015 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18906 | hp2 | a0001 | c0003 | t0004 | g0150 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18950 | hp2 | a0001 | c0001 | t0010 | g0155 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18960 | hp1 | a0002 | c0005 | t0001 | g0110 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18961 | hp2 | a0002 | c0005 | t0003 | g0103 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18966 | hp1 | a0002 | c0005 | t0001 | g0076 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18974 | hp2 | a0002 | c0005 | t0001 | g0087 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18975 | hp2 | a0002 | c0005 | t0001 | g0085 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18980 | hp1 | a0001 | c0021 | t0001 | g0200 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18980 | hp2 | a0002 | c0005 | t0001 | g0255 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18997 | hp1 | a0023 | c0033 | t0001 | g0109 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18997 | hp2 | a0001 | c0024 | t0001 | g0191 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19011 | hp2 | a0024 | c0030 | t0001 | g0072 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19030 | hp1 | a0001 | c0002 | t0006 | g0047 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19030 | hp2 | a0001 | c0037 | t0027 | g0058 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19043 | hp1 | a0001 | c0032 | t0001 | g0120 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19043 | hp2 | a0001 | c0046 | t0006 | g0006 | 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 | g0081 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19088 | hp2 | a0001 | c0001 | t0015 | g0117 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19240 | hp1 | a0001 | c0015 | t0005 | g0276 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA19240 | hp2 | a0001 | c0001 | t0023 | g0079 | AFR | YRI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20129 | hp1 | a0001 | c0003 | t0010 | g0144 | AFR | ASW | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20129 | hp2 | a0001 | c0004 | t0005 | g0013 | AFR | ASW | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | TSI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20752 | hp2 | a0001 | c0008 | t0009 | g0030 | EUR | TSI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20805 | hp1 | a0001 | c0002 | t0007 | g0226 | EUR | TSI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20805 | hp2 | a0001 | c0020 | t0001 | g0246 | EUR | TSI | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0279 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02109 | hp2 | a0001 | c0003 | t0004 | g0295 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02486 | hp1 | a0001 | c0012 | t0001 | g0071 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG02486 | hp2 | a0004 | c0011 | t0011 | g0028 | 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 | g0192 | AFR | ACB | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG03471 | hp1 | a0001 | c0036 | t0006 | g0006 | 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 | g0106 | AFR | USA | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
HG06807 | hp2 | a0022 | c0025 | t0001 | g0128 | AFR | USA | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20300 | hp1 | a0001 | c0001 | t0028 | g0054 | AFR | USA | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | USA | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA21309 | hp1 | a0001 | c0002 | t0018 | g0052 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0040 | REF | REF | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | TSC2_chr16_2042985_2094491 | TSC2 | chr16 | 2042985 | 2094491 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:2048740 | C | T | 1 | a0009 | 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 | a0020 | 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 | a0020 | 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 | a0008 | 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 | a0021 | 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 | a0007 a0019 |
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 | a0018 | 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 | a0024 | 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 | a0010 | 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 | a0014 | 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 | a0007 a0015 a0019 |
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 | a0004 a0006 a0012 others(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 | a0017 | 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 | a0013 | 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 | a0007 | 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 | a0006 a0016 a0017 |
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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | a0001c0050 a0006c0018 |
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 | a0001c0008 a0001c0048 a0001c0049 |
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 | a0017c0045 | 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 | a0001c0004 a0001c0008 a0001c0014 others(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 | a0001c0007 a0001c0032 |
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 | a0018c0044 | 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 | a0001c0004 a0001c0015 |
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 | a0001c0002 a0001c0003 a0001c0004 others(20): Show |
93 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(90): 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 | a0001c0008 a0001c0014 a0001c0039 |
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 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | a0001c0002t0006 a0001c0002t0018 a0001c0036t0006 others(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 | a0001c0008t0009 a0001c0014t0009 a0001c0039t0001 |
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 | a0001c0001t0007 a0001c0002t0007 |
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 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0005 others(14): Show |
56 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(53): 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 | a0001c0001t0015 a0004c0011t0011 a0004c0023t0011 others(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 | a0013c0040t0033 | 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 | a0001c0001t0003 a0001c0001t0017 a0001c0051t0003 others(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 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0006 others(6): Show |
37 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(34): 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 | a0001c0002t0005 a0001c0002t0018 a0001c0004t0005 others(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 | a0016c0029t0031 | 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 | a0006c0018t0030 | 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 | a0006c0018t0032 | 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 | a0001c0001t0016 a0001c0001t0026 a0001c0002t0016 others(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 | a0001c0003t0004 a0001c0008t0009 a0001c0014t0009 |
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 | a0001c0001t0008 a0001c0001t0028 a0018c0044t0008 |
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 | a0001c0001t0010 a0001c0003t0010 a0001c0007t0012 others(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 | a0001c0001t0016 a0001c0002t0016 a0001c0003t0004 |
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 | a0001c0001t0002 a0001c0001t0016 a0001c0002t0002 others(28): Show |
77 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(74): 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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:2048067 | TAAGTGGC others(14): Show |
T | 1 | a0017c0045t0025g0298 | 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 | a0001c0050t0035g0297 | 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 | a0001c0052t0001g0016 | 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 | a0001c0001t0024g0017 | 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 | a0001c0003t0004g0295 a0001c0003t0004g0296 |
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 | a0001c0004t0005g0015 | 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 | a0001c0001t0016g0294 | 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 | a0001c0001t0001g0293 | 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 | a0001c0017t0001g0292 | 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 | a0001c0002t0006g0018 | 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 | a0001c0001t0003g0291 | 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 | a0017c0045t0025g0298 | 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 | a0001c0050t0035g0297 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0272 a0001c0002t0002g0275 a0001c0002t0002g0278 others(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 | a0001c0002t0002g0021 a0001c0002t0006g0022 a0001c0007t0012g0005 others(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 | a0004c0011t0011g0025 a0004c0011t0011g0028 a0004c0011t0029g0027 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0271 | 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 | a0001c0002t0002g0021 a0001c0002t0006g0022 a0001c0007t0012g0005 others(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 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0142 a0001c0003t0004g0141 a0001c0003t0004g0143 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 a0017c0045t0025g0298 |
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 | a0001c0002t0006g0022 a0001c0007t0012g0005 a0001c0007t0012g0023 others(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 | a0001c0001t0001g0033 a0001c0008t0009g0030 a0001c0008t0009g0031 others(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 | a0001c0004t0005g0139 | 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 | a0013c0040t0033g0266 | 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 | a0016c0029t0031g0035 | 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 | a0007c0013t0010g0136 a0007c0013t0010g0138 a0019c0028t0010g0137 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0264 others(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 | a0016c0029t0031g0035 | 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 | a0001c0001t0001g0270 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0133 a0001c0001t0001g0260 a0001c0001t0001g0261 others(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 | 44 | a0001c0001t0001g0053 a0001c0001t0001g0134 a0001c0001t0001g0142 others(41): Show |
45 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(42): 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0003g0269 a0001c0002t0006g0022 a0001c0007t0012g0005 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0056 |
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 | a0001c0001t0001g0057 | 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 | a0001c0002t0006g0022 a0001c0007t0012g0005 a0001c0007t0012g0023 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0002t0002g0021 a0004c0011t0011g0025 a0004c0011t0011g0028 others(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 | a0001c0004t0005g0139 | 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 | a0001c0037t0027g0058 | 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 | a0001c0001t0001g0033 a0001c0002t0002g0007 a0001c0002t0002g0021 others(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 | a0001c0001t0001g0131 a0015c0042t0002g0132 |
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 | 22 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0037 others(19): Show |
22 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(19): 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0013g0259 others(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 | a0001c0019t0002g0051 | 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 |
20 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0050 others(17): Show |
20 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(17): 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 | a0001c0002t0002g0037 a0001c0002t0006g0036 |
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 | a0001c0002t0018g0052 | 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 | 23 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0037 others(20): Show |
23 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(20): 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(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 | a0001c0001t0002g0039 a0001c0019t0002g0038 a0001c0019t0002g0051 |
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 | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(159): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): 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 | a0001c0003t0004g0125 a0001c0003t0004g0126 a0015c0042t0002g0132 |
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 | a0001c0002t0018g0052 | 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 | a0001c0008t0009g0063 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0248 a0001c0001t0001g0251 others(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 | a0001c0001t0016g0294 | 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 | a0001c0002t0002g0037 a0001c0002t0002g0050 a0001c0002t0005g0049 |
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 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0020t0001g0246 |
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 | a0001c0002t0016g0127 a0022c0025t0001g0128 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.336+33G>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 4/41 | chr16 | 2053485 | |||||||
chr16:2054233 | C | T | 1 | a0001c0001t0001g0124 | 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 | a0001c0002t0002g0062 | 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 | a0013c0040t0033g0266 | 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 | a0001c0001t0001g0142 a0001c0003t0004g0141 a0001c0003t0004g0143 others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0008g0123 | 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 | a0001c0001t0001g0241 a0005c0010t0001g0242 a0005c0010t0001g0243 others(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 | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(219): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): 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 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
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 | a0001c0003t0004g0141 | 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 | a0001c0001t0019g0240 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0113 | 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 | a0001c0001t0016g0294 a0001c0002t0006g0041 a0001c0002t0016g0127 others(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 | a0001c0001t0003g0262 | 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 | 39 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(36): Show |
40 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.482-68C>G | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 5/41 | chr16 | 2055334 | |||||||
chr16:2055399 | C | T | 20 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0037 others(17): Show |
20 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(17): 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 | a0001c0001t0001g0142 | 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 | a0020c0054t0001g0112 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0056 |
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 | a0001c0001t0001g0167 | 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 | a0001c0002t0006g0018 | 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 | a0001c0003t0004g0143 | 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 | 47 | a0001c0001t0001g0165 a0001c0001t0001g0241 a0001c0001t0002g0039 others(44): Show |
50 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(47): 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 | a0001c0001t0001g0111 a0001c0001t0001g0151 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0007g0252 a0001c0003t0004g0295 a0001c0003t0004g0296 |
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 | a0006c0018t0030g0121 a0006c0018t0032g0122 |
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 | a0006c0018t0030g0121 a0006c0018t0032g0122 a0016c0029t0031g0035 |
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 | a0001c0001t0001g0265 | 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 | a0004c0011t0011g0025 a0004c0011t0011g0028 a0004c0011t0029g0027 others(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 | a0007c0013t0010g0136 a0007c0013t0010g0138 |
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 | a0001c0001t0001g0142 | 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 | a0001c0001t0020g0169 | 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 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0173 others(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 | a0001c0007t0002g0042 a0001c0007t0002g0043 a0001c0007t0012g0005 others(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 | 10 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0037 others(7): Show |
10 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(7): 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 | a0007c0013t0010g0136 a0007c0013t0010g0138 |
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 | a0013c0040t0033g0266 | 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 | a0001c0007t0002g0042 a0001c0007t0002g0043 a0001c0007t0012g0005 others(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 | a0001c0001t0001g0233 a0001c0001t0001g0293 a0001c0001t0003g0001 others(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 | a0015c0042t0002g0132 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | 35 | a0001c0001t0001g0010 a0001c0001t0001g0151 a0001c0001t0001g0165 others(32): Show |
37 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(34): 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 | a0001c0003t0004g0141 a0001c0003t0004g0143 a0001c0003t0004g0145 others(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 | a0023c0033t0001g0109 | 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 | a0001c0002t0006g0041 a0001c0002t0016g0127 a0022c0025t0001g0128 |
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 | a0001c0032t0001g0120 | 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 | a0001c0001t0003g0230 | 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 | a0001c0007t0002g0043 a0001c0007t0012g0005 a0001c0007t0012g0023 others(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 | a0001c0001t0016g0294 | 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 | a0001c0022t0001g0108 | 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 | a0001c0002t0006g0041 a0001c0002t0016g0127 a0022c0025t0001g0128 |
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 | a0001c0032t0001g0120 a0001c0037t0027g0058 |
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 | a0001c0002t0006g0036 | 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 | a0001c0001t0008g0154 a0001c0001t0008g0256 |
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 | a0020c0054t0001g0112 | 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 | a0020c0054t0001g0112 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0067 | 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 | a0006c0018t0030g0121 a0006c0018t0032g0122 a0016c0029t0031g0035 |
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 | a0001c0002t0002g0021 a0004c0011t0011g0025 a0004c0011t0011g0028 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0229 |
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 | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(159): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): 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 | a0001c0001t0001g0106 a0001c0001t0001g0174 |
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 | a0016c0029t0031g0035 | 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 | a0001c0048t0001g0029 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0003g0107 a0001c0001t0003g0291 a0001c0001t0016g0294 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0178 a0001c0001t0003g0177 others(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 | a0001c0001t0001g0124 a0001c0001t0017g0175 a0001c0003t0010g0144 |
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 | a0020c0054t0001g0112 | 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 | a0001c0007t0002g0042 a0001c0007t0002g0043 a0001c0007t0012g0005 others(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 | a0001c0002t0002g0007 a0001c0002t0002g0059 a0001c0002t0002g0060 others(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 | 151 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(148): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0001t0001g0004 a0001c0001t0001g0153 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0001c0001t0001g0174 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0007t0002g0043 a0001c0007t0012g0005 a0001c0007t0012g0023 others(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 | a0005c0010t0001g0244 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0093 others(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 | a0020c0054t0001g0112 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0218 | 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 | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(148): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): 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 | a0001c0008t0009g0030 a0001c0008t0009g0031 a0001c0008t0009g0034 others(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 | a0001c0002t0002g0021 a0004c0011t0011g0025 a0004c0011t0011g0028 others(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 | a0001c0050t0035g0297 | 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 | a0001c0050t0035g0297 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(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 | a0001c0032t0001g0120 | 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 | a0001c0001t0003g0269 | 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 | a0001c0001t0001g0183 | 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 | a0020c0054t0001g0112 | 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 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0173 others(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 | a0001c0002t0002g0021 a0004c0011t0011g0025 a0004c0011t0011g0028 others(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 | a0001c0001t0001g0185 | 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 | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(162): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): 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 | a0001c0001t0001g0217 | 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 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0062 |
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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0003g0107 | 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 | a0001c0001t0001g0251 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0002t0016g0127 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0248 a0002c0005t0003g0103 |
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 | a0001c0002t0002g0287 | 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 | a0001c0001t0001g0185 | 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 | a0001c0002t0002g0007 a0001c0002t0002g0059 a0001c0002t0002g0060 others(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 | a0001c0003t0004g0141 a0001c0003t0004g0143 a0001c0003t0004g0145 others(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 | a0001c0001t0001g0092 | 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 | a0001c0002t0006g0018 | 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 | a0001c0003t0004g0147 | 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 | a0001c0003t0004g0141 a0001c0003t0004g0143 a0001c0003t0004g0145 others(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 | a0001c0001t0001g0133 | 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 | a0004c0011t0011g0025 a0004c0011t0011g0028 a0004c0011t0029g0027 others(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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0111 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0009t0014g0009 a0001c0009t0014g0140 a0016c0029t0031g0035 others(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 | a0001c0001t0001g0133 | 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 | a0001c0050t0035g0297 a0006c0018t0030g0121 a0006c0018t0032g0122 |
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 | a0001c0002t0002g0275 a0001c0002t0002g0278 a0001c0002t0002g0279 others(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 | a0016c0029t0031g0035 a0017c0045t0025g0298 |
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 | a0001c0009t0014g0009 a0001c0009t0014g0140 a0016c0029t0031g0035 others(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 | a0001c0007t0002g0042 a0001c0007t0002g0043 a0001c0007t0012g0005 others(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 | a0001c0001t0015g0117 | 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 | a0001c0001t0003g0230 | 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 | a0001c0002t0002g0287 | 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 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0111 others(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 | a0001c0008t0009g0030 a0001c0008t0009g0031 a0001c0008t0009g0034 others(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 | a0001c0001t0010g0155 | 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 | a0006c0018t0030g0121 a0006c0018t0032g0122 a0016c0029t0031g0035 |
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 | a0001c0001t0001g0124 | 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 | a0009c0055t0003g0186 | 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 | a0001c0002t0016g0127 | 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 | a0001c0001t0001g0187 a0001c0001t0038g0176 a0001c0002t0007g0159 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0216 a0001c0001t0001g0222 others(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 | a0016c0029t0031g0035 | 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 | a0001c0001t0001g0091 a0001c0003t0004g0141 a0001c0003t0004g0143 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0239 others(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 | 45 | a0001c0001t0001g0091 a0001c0001t0002g0039 a0001c0001t0002g0046 others(42): Show |
46 | HG00280.hp1 HG01070.hp2 HG01074.hp1 others(43): 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 | a0001c0003t0004g0149 a0001c0007t0002g0042 a0001c0007t0002g0043 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0016g0294 a0001c0002t0016g0127 |
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 | 10 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0037 others(7): Show |
10 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(7): 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 | a0001c0008t0009g0030 a0001c0008t0009g0031 a0001c0008t0009g0034 others(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 | a0016c0029t0031g0035 a0017c0045t0025g0298 |
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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): 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 | a0001c0001t0024g0017 a0001c0002t0002g0021 a0001c0002t0006g0018 others(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 | a0001c0001t0022g0164 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0241 a0001c0001t0003g0107 others(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 | 26 | a0001c0001t0001g0064 a0001c0001t0001g0119 a0001c0001t0001g0135 others(23): Show |
26 | HG00280.hp1 HG00558.hp2 HG00741.hp2 others(23): 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 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0010g0155 | 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 | a0004c0011t0029g0027 | 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 | a0001c0002t0002g0021 a0001c0002t0006g0018 a0001c0002t0006g0022 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0050t0035g0297 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0261 | 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 | a0006c0018t0030g0121 a0006c0018t0032g0122 |
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 | a0001c0002t0016g0127 | 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 | a0001c0001t0016g0294 a0001c0002t0016g0127 |
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 | a0001c0001t0003g0197 a0017c0045t0025g0298 |
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 | a0001c0003t0004g0143 a0001c0003t0004g0145 a0001c0003t0004g0146 others(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 | a0001c0003t0004g0143 a0001c0003t0004g0145 a0001c0003t0004g0146 others(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 | a0001c0002t0018g0052 | 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 | a0001c0003t0004g0143 a0001c0003t0004g0145 a0001c0003t0004g0146 others(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 | a0001c0003t0004g0143 a0001c0003t0004g0145 a0001c0003t0004g0146 others(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 | a0001c0008t0009g0030 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0015c0042t0002g0132 | 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 | a0001c0037t0027g0058 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0017c0045t0025g0298 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0241 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0001t0001g0167 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0001t0016g0294 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0007t0002g0042 a0001c0007t0002g0043 a0001c0007t0012g0005 others(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 | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): 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 | a0001c0004t0005g0139 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0174 a0001c0001t0001g0258 others(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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(130): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): 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 | a0001c0001t0001g0114 a0001c0001t0001g0180 a0001c0001t0001g0181 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0088 a0001c0001t0001g0089 others(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 | a0001c0003t0004g0141 a0001c0003t0004g0143 a0001c0003t0004g0145 others(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 | a0001c0012t0001g0130 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0102 a0001c0001t0001g0131 |
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 | 66 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(63): Show |
68 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(65): 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0162 a0001c0001t0034g0160 |
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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0210 a0001c0001t0003g0107 others(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 | a0001c0001t0001g0264 | 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 | 11 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0001t0024g0017 others(8): Show |
11 | HG00280.hp1 HG00741.hp2 HG01074.hp1 others(8): 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 | a0001c0008t0009g0063 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0180 a0001c0015t0005g0276 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0157 others(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 | a0001c0007t0002g0042 a0001c0007t0002g0043 a0001c0007t0012g0005 others(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 | a0001c0003t0004g0141 a0001c0003t0004g0143 a0001c0003t0004g0145 others(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 | a0001c0003t0004g0141 a0001c0003t0004g0143 a0001c0003t0004g0145 others(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 | a0001c0003t0004g0141 a0001c0003t0004g0143 a0001c0003t0004g0145 others(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 | a0001c0001t0001g0119 a0023c0033t0001g0109 |
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 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0173 |
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 | a0001c0050t0035g0297 a0006c0018t0030g0121 a0006c0018t0032g0122 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0142 a0001c0001t0024g0017 others(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 | a0001c0001t0001g0209 | 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 | a0001c0002t0007g0159 a0001c0002t0007g0163 |
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 | a0001c0001t0034g0160 a0001c0003t0004g0150 a0004c0011t0011g0025 others(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 | a0001c0001t0001g0196 | 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 | a0001c0015t0005g0277 a0022c0025t0001g0128 |
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 | 117 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0053 others(114): Show |
124 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(121): 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0134 | 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 | a0001c0002t0006g0047 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0129 |
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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0020t0001g0246 |
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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 a0007c0013t0010g0136 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(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 | a0004c0011t0011g0025 a0004c0011t0011g0028 a0004c0011t0029g0027 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0074 | 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 | a0007c0013t0010g0136 a0007c0013t0010g0138 a0019c0028t0010g0137 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0015g0117 |
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 | a0001c0001t0001g0133 | 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 | a0001c0002t0002g0021 a0001c0007t0012g0005 a0001c0007t0012g0023 others(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 | a0001c0001t0001g0271 | 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 | a0001c0032t0001g0120 | 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 | a0001c0001t0024g0017 | 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 | a0001c0001t0001g0268 a0001c0001t0001g0270 |
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 | a0017c0045t0025g0298 | 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 | a0001c0001t0016g0294 | 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 | a0001c0053t0001g0168 | 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 | a0001c0001t0016g0294 a0001c0002t0002g0281 a0001c0002t0006g0018 others(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 | a0017c0045t0025g0298 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0162 others(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 | a0001c0001t0016g0294 a0001c0002t0002g0281 a0001c0002t0006g0018 others(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 | a0007c0013t0010g0136 a0007c0013t0010g0138 a0019c0028t0010g0137 |
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 | a0001c0037t0027g0058 | 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 | a0001c0002t0002g0287 | 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 | a0001c0001t0016g0294 | 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 | a0001c0001t0016g0294 a0001c0002t0002g0281 a0001c0002t0016g0127 others(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 | a0001c0002t0002g0050 a0001c0003t0004g0141 a0001c0003t0004g0143 others(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 | a0001c0001t0017g0175 | 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 | a0001c0047t0001g0077 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 a0001c0037t0027g0058 |
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 | a0001c0032t0001g0120 | 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 | a0001c0002t0006g0047 | 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 | a0001c0001t0003g0231 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0090 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0001t0016g0294 a0001c0002t0002g0281 a0001c0002t0016g0127 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0017c0045t0025g0298 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0124 | 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 | a0001c0002t0016g0127 | 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 | a0001c0001t0016g0294 a0001c0002t0002g0281 a0001c0002t0016g0127 others(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 | a0004c0011t0011g0025 a0004c0011t0011g0028 a0004c0011t0029g0027 others(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 | a0001c0003t0004g0147 | 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 | a0001c0008t0009g0063 | 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 | a0001c0014t0009g0048 | 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 | a0001c0001t0016g0294 a0001c0002t0002g0281 a0001c0002t0006g0018 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0102 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0205 a0001c0001t0001g0239 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0001t0001g0093 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0091 a0001c0001t0001g0097 a0001c0001t0001g0151 others(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 | 29 | a0001c0001t0001g0074 a0001c0001t0001g0115 a0001c0001t0001g0118 others(26): Show |
30 | HG00408.hp1 HG01175.hp1 HG01261.hp2 others(27): 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 | a0001c0001t0001g0091 a0001c0001t0001g0162 a0001c0001t0034g0160 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0182 a0001c0001t0001g0211 others(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 | a0007c0013t0010g0136 a0007c0013t0010g0138 a0019c0028t0010g0137 |
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 | a0001c0032t0001g0120 a0001c0050t0035g0297 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0111 a0001c0001t0001g0113 others(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 | a0007c0013t0010g0136 a0007c0013t0010g0138 a0019c0028t0010g0137 |
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 | a0001c0001t0001g0178 a0001c0001t0001g0205 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0162 others(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 | a0004c0023t0011g0156 | 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 | a0001c0001t0001g0178 a0001c0001t0001g0239 |
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 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0162 others(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 | a0001c0037t0027g0058 | 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 | a0001c0001t0001g0102 | 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 | a0001c0037t0027g0058 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0016g0294 | 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 | a0001c0053t0001g0168 | 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 | a0001c0001t0016g0294 a0001c0002t0016g0127 a0001c0004t0005g0013 others(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 | a0001c0002t0006g0047 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0182 a0001c0001t0001g0211 |
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 | a0001c0001t0003g0215 | 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 | a0001c0001t0024g0017 | 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 | a0013c0040t0033g0266 | 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 | a0007c0013t0010g0136 a0007c0013t0010g0138 a0019c0028t0010g0137 |
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 | a0001c0001t0001g0090 | 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 | a0001c0001t0016g0294 a0001c0002t0016g0127 a0001c0004t0005g0013 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0241 a0001c0002t0006g0018 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 a0001c0050t0035g0297 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0001t0001g0093 | 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 | a0006c0018t0030g0121 a0006c0018t0032g0122 |
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 | a0001c0003t0004g0125 a0001c0003t0004g0126 a0015c0042t0002g0132 |
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 | a0001c0002t0016g0127 a0001c0004t0005g0013 a0001c0004t0005g0015 others(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 | a0001c0001t0001g0220 | 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 | a0001c0008t0009g0034 | 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 | a0014c0043t0001g0214 | 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 | a0004c0011t0011g0025 a0004c0011t0011g0028 a0004c0011t0029g0027 others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0134 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0170 | 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 | 7 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0037 others(4): Show |
7 | HG00280.hp1 HG01074.hp1 HG01081.hp1 others(4): 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 | a0001c0001t0001g0257 | 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 | a0001c0002t0002g0275 a0001c0002t0002g0278 |
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 | a0001c0001t0001g0057 | 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 | a0001c0048t0001g0029 | 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 | a0001c0037t0027g0058 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0057 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0032t0001g0120 | 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 | a0023c0033t0001g0109 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0088 | 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 | a0022c0025t0001g0128 | 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 | a0006c0018t0030g0121 a0006c0018t0032g0122 |
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 | a0001c0051t0003g0232 | 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 | a0001c0001t0015g0238 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0006c0018t0030g0121 a0006c0018t0032g0122 a0017c0045t0025g0298 |
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 | a0001c0012t0001g0071 a0001c0012t0001g0078 a0001c0012t0001g0130 |
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 | a0016c0029t0031g0035 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0041 others(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 | a0001c0002t0002g0275 a0001c0002t0002g0278 a0001c0002t0002g0279 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0097 a0001c0001t0001g0151 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0162 a0001c0001t0034g0160 others(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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0178 a0001c0001t0001g0205 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0170 |
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 | a0001c0001t0016g0294 | 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 | a0001c0002t0002g0288 | 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 | a0001c0004t0005g0013 a0001c0004t0005g0015 a0001c0004t0005g0139 others(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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0157 others(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 | a0001c0001t0015g0238 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0003g0215 a0001c0001t0019g0240 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0133 a0001c0001t0003g0231 others(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 | a0001c0001t0001g0268 a0001c0001t0001g0270 |
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 | a0001c0001t0001g0134 | 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 | a0001c0002t0002g0281 | 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 | a0001c0001t0001g0247 a0001c0001t0001g0293 a0001c0001t0013g0219 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0165 a0001c0001t0001g0166 others(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 | a0023c0033t0001g0109 | 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 | 89 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0162 others(86): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0059 others(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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0223 | 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 | a0015c0042t0002g0132 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0092 others(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 | a0001c0001t0038g0176 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0151 others(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 | a0001c0009t0014g0009 a0001c0009t0014g0140 |
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 | a0001c0001t0001g0075 | 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 | a0001c0007t0002g0042 a0001c0007t0002g0043 |
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 | a0001c0001t0020g0169 | 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 | a0001c0001t0001g0153 a0001c0001t0001g0229 |
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 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0092 | 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 | a0006c0018t0030g0121 a0006c0018t0032g0122 |
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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0180 a0001c0001t0001g0213 a0001c0001t0001g0258 others(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 | a0003c0006t0002g0290 | 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 | a0001c0002t0007g0227 | 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 | a0001c0001t0001g0153 a0001c0001t0001g0194 a0001c0001t0001g0229 |
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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0192 |
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 | a0001c0003t0004g0296 | 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 | a0001c0007t0012g0005 a0001c0007t0012g0023 a0001c0007t0012g0024 |
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 | a0001c0001t0016g0294 | 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 | a0001c0007t0002g0042 a0001c0007t0002g0043 a0001c0007t0012g0005 others(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 | a0001c0001t0003g0073 | 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 | a0001c0007t0002g0042 a0001c0007t0002g0043 a0001c0007t0012g0005 others(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 | a0001c0001t0001g0097 | 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 | a0001c0014t0009g0193 | 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 | a0001c0015t0005g0277 | 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 | 48 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0001t0016g0294 others(45): Show |
50 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(47): 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 | a0001c0037t0027g0058 | 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 | a0001c0001t0023g0079 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0024g0017 | 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 | a0001c0048t0001g0029 | 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 | a0001c0001t0019g0240 | 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 | a0006c0018t0030g0121 a0006c0018t0032g0122 |
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 | a0001c0001t0001g0260 | 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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0002c0005t0001g0076 a0002c0005t0001g0085 a0002c0005t0001g0087 others(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 | a0001c0037t0027g0058 | 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 | a0001c0008t0009g0030 a0001c0008t0009g0031 a0001c0008t0009g0034 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0111 a0001c0001t0001g0115 others(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 | a0004c0011t0011g0025 a0004c0011t0011g0028 a0004c0011t0029g0027 others(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 | a0001c0007t0012g0023 | 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 | a0001c0052t0001g0016 | 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 | a0001c0001t0001g0224 | 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 | a0001c0017t0001g0207 a0001c0017t0001g0292 |
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 | a0001c0001t0001g0202 | 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 | a0007c0013t0010g0136 a0007c0013t0010g0138 a0015c0042t0002g0132 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0093 | 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 | a0006c0018t0030g0121 a0006c0018t0032g0122 a0016c0029t0031g0035 others(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 | a0001c0001t0001g0134 a0001c0001t0016g0294 a0001c0002t0016g0127 others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0010g0155 | 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 | a0001c0004t0005g0280 | 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 | a0001c0001t0024g0017 | 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 | a0001c0001t0016g0294 a0001c0002t0016g0127 a0001c0009t0014g0009 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0260 others(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 | a0001c0001t0016g0294 a0001c0009t0014g0009 a0001c0009t0014g0140 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0001g0171 others(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 | a0004c0023t0011g0156 a0006c0018t0030g0121 a0006c0018t0032g0122 others(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 | a0001c0002t0006g0018 a0001c0002t0006g0022 a0001c0002t0006g0036 others(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 | a0001c0001t0024g0017 | 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 | 65 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0001t0016g0294 others(62): Show |
69 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(66): 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 | a0001c0001t0003g0234 | 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 | a0007c0013t0010g0136 a0007c0013t0010g0138 a0019c0028t0010g0137 |
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 | a0001c0001t0001g0134 | 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 | a0001c0003t0004g0125 a0001c0003t0004g0126 a0001c0003t0004g0141 others(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 | a0001c0001t0001g0195 | 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 | a0001c0002t0016g0127 | 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 | a0001c0002t0016g0127 | 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 | a0001c0002t0002g0060 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0057 a0001c0001t0001g0065 others(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 | 58 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0037 others(55): Show |
61 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(58): 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 | a0001c0001t0016g0294 | 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 | a0001c0009t0014g0009 a0001c0009t0014g0140 a0001c0037t0027g0058 |
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 | a0001c0001t0013g0219 | 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 | a0001c0001t0001g0066 | 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 | a0004c0011t0011g0025 a0004c0011t0011g0028 a0004c0011t0029g0027 others(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 | a0001c0001t0001g0260 | 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 | a0001c0001t0016g0294 a0001c0009t0014g0009 a0001c0009t0014g0140 others(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 | a0012c0035t0011g0026 a0013c0040t0033g0266 |
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 | a0011c0038t0003g0098 | 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 | 71 | a0001c0001t0001g0151 a0001c0001t0002g0039 a0001c0001t0002g0046 others(68): Show |
76 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(73): 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 | a0001c0001t0001g0194 | 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 | 47 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0007 others(44): Show |
50 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.5260-49C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 41/41 | chr16 | 2088397 | |||||||
chr16:2088421 | C | G | 60 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0002t0002g0007 others(57): Show |
64 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(61): 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 | a0001c0037t0027g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5260-15C>T | TSC2 | ENSG00000103197.19 | transcript | ENST00000219476.9 | protein_coding | 41/41 | chr16 | 2088431 |