Item | Value |
---|---|
geneid | 7042 |
ensemblid | ENSG00000092969.12 |
hgncid | 11768 |
symbol | TGFB2 |
name | transforming growth factor beta 2 |
refseq_nuc | NM_003238.6 |
refseq_prot | NP_003229.1 |
ensembl_nuc | ENST00000366930.9 |
ensembl_prot | ENSP00000355897.4 |
mane_status | MANE Select |
chr | chr1 |
start | 218345336 |
end | 218444619 |
strand | + |
ver | v1.2 |
region | chr1:218345336-218444619 |
region5000 | chr1:218340336-218449619 |
regionname0 | TGFB2_chr1_218345336_218444619 |
regionname5000 | TGFB2_chr1_218340336_218449619 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 414 | 288 | 82 | 47 | 121 | 6 | 30 | 95 | TGFB2_chr1_218340336_218449619 | TGFB2 | MHYCV others(409): Show |
chr1 | 218340336 | 218449619 |
a0002 | 0/0 | 414 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | MHYCV others(409): Show |
chr1 | 218340336 | 218449619 |
a0003 | 0/0 | 414 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | MHYCV others(409): Show |
chr1 | 218340336 | 218449619 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1242 | 287 | 82 | 47 | 121 | 6 | 29 | TGFB2_chr1_218340336_218449619 | TGFB2 | ATGCA others(1237): Show |
chr1 | 218340336 | 218449619 | ||
a0001c0002 | 0/0 | 1242 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | ATGCA others(1237): Show |
chr1 | 218340336 | 218449619 | ||
a0002c0003 | 0/0 | 1242 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | ATGCA others(1237): Show |
chr1 | 218340336 | 218449619 | ||
a0003c0004 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | ATGCA others(1237): Show |
chr1 | 218340336 | 218449619 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5868 | 48 | 9 | 13 | 13 | 2 | 10 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5863): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0002 | 0/0 | 5866 | 35 | 2 | 2 | 26 | 1 | 4 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0003 | 0/0 | 5872 | 28 | 11 | 4 | 10 | 0 | 3 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0004 | 0/0 | 5870 | 23 | 4 | 4 | 15 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5865): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0005 | 0/0 | 5869 | 8 | 0 | 0 | 6 | 2 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5864): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0006 | 0/0 | 5867 | 8 | 0 | 5 | 2 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0007 | 0/0 | 5867 | 8 | 3 | 2 | 3 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0008 | 0/0 | 5866 | 7 | 0 | 6 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0009 | 0/0 | 5871 | 6 | 1 | 1 | 2 | 0 | 2 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5866): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0010 | 0/0 | 5880 | 5 | 0 | 0 | 5 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5875): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0011 | 0/0 | 5870 | 4 | 3 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5865): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0012 | 0/0 | 5874 | 4 | 0 | 0 | 4 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5869): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0013 | 0/0 | 5872 | 3 | 2 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0014 | 0/0 | 5869 | 3 | 2 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5864): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0015 | 0/0 | 5868 | 3 | 0 | 0 | 2 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5863): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0016 | 0/0 | 5868 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5863): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0017 | 0/0 | 5863 | 3 | 0 | 0 | 3 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5858): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0018 | 0/0 | 5880 | 3 | 3 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5875): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0019 | 0/0 | 5874 | 3 | 2 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5869): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0020 | 0/0 | 5872 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0021 | 0/0 | 5880 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5875): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0022 | 0/0 | 5873 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5868): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0023 | 0/0 | 5871 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5866): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0024 | 0/0 | 5871 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5866): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0025 | 0/0 | 5870 | 2 | 0 | 1 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5865): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0026 | 0/0 | 5883 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5878): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0027 | 0/0 | 5878 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5873): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0028 | 0/0 | 5880 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5875): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0029 | 0/0 | 5876 | 2 | 2 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5871): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0030 | 0/0 | 5882 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5877): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0031 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5869): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0032 | 0/0 | 5872 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0033 | 0/0 | 5870 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5865): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0034 | 0/0 | 5876 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5871): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0035 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5869): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0036 | 0/0 | 5874 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5869): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0037 | 0/0 | 5869 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5864): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0038 | 0/0 | 5873 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5868): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0039 | 0/0 | 5872 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0040 | 0/0 | 5872 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0041 | 0/0 | 5871 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5866): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0042 | 0/0 | 5870 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5865): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0043 | 0/0 | 5870 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5865): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0044 | 0/0 | 5870 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5865): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0045 | 0/0 | 5870 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5865): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0046 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0047 | 0/0 | 5874 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5869): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0048 | 0/0 | 5870 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5865): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0049 | 0/0 | 5876 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5871): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0050 | 0/0 | 5865 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5860): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0051 | 0/0 | 5865 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5860): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0052 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5860): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0053 | 0/0 | 5866 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0054 | 0/0 | 5867 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0055 | 0/0 | 5867 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0056 | 0/0 | 5875 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5870): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0057 | 0/0 | 5868 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5863): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0058 | 0/0 | 5865 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5860): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0059 | 0/0 | 5868 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5863): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0060 | 0/0 | 5868 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5863): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0061 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5869): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0062 | 0/0 | 5867 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0063 | 0/0 | 5867 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0064 | 0/0 | 5866 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0065 | 0/0 | 5866 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0066 | 0/0 | 5868 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5863): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0067 | 0/0 | 5866 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0068 | 0/0 | 5866 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0069 | 0/0 | 5866 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0070 | 0/0 | 5867 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0071 | 0/0 | 5867 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0072 | 0/0 | 5867 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0073 | 0/0 | 5866 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0074 | 0/0 | 5884 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5879): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0075 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5878): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0076 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5872): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0077 | 0/0 | 5878 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5873): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0078 | 0/0 | 5876 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5871): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0079 | 0/0 | 5878 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5873): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0080 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5877): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0081 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5869): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0082 | 0/0 | 5872 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0083 | 0/0 | 5872 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0084 | 0/1 | 5867 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5862): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0085 | 0/0 | 5878 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5873): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0086 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5872): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0087 | 0/0 | 5888 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5883): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0088 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5878): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0089 | 0/0 | 5881 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5876): Show |
chr1 | 218340336 | 218449619 |
a0001c0001t0090 | 0/0 | 5874 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5869): Show |
chr1 | 218340336 | 218449619 |
a0001c0002t0002 | 0/0 | 5866 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0002c0003t0002 | 0/0 | 5866 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5861): Show |
chr1 | 218340336 | 218449619 |
a0003c0004t0003 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | GATGT others(5867): Show |
chr1 | 218340336 | 218449619 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0009g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0011g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0012g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0012g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0012g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0012g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0013g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0014g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0014g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0015g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0015g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0015g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0016g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0016g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0016g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0017g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0017g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0017g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0018g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0018g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0018g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0019g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0019g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0019g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0020g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0021g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0021g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0022g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0022g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0023g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0023g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0024g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0024g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0025g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0025g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0026g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0026g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0027g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0027g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0028g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0028g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0029g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0029g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0030g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0030g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0031g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0032g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0033g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0034g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0035g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0036g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0037g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0038g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0039g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0040g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0041g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0042g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0043g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0044g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0045g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0046g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0047g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0048g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0049g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0050g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0051g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0052g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0053g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0054g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0055g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0056g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0057g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0058g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0059g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0060g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0061g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0062g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0063g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0064g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0065g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0066g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0067g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0068g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0069g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0070g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0071g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0072g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0073g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0074g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0075g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0076g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0077g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0078g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0079g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0080g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0081g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0082g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0083g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0084g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0085g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0086g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0087g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0088g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0089g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0001t0090g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
a0003c0004t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0005 | g0089 | EUR | GBR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00438 | hp2 | a0001 | c0001 | t0022 | g0214 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00639 | hp2 | a0002 | c0003 | t0002 | g0080 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0182 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG00741 | hp2 | a0001 | c0001 | t0047 | g0241 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01069 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0193 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01081 | hp2 | a0001 | c0001 | t0064 | g0134 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01109 | hp2 | a0001 | c0001 | t0011 | g0225 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01243 | hp1 | a0001 | c0001 | t0026 | g0279 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01243 | hp2 | a0001 | c0001 | t0019 | g0272 | AMR | PUR | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0183 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0101 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0078 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01261 | hp2 | a0001 | c0001 | t0009 | g0259 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0079 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01358 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01358 | hp2 | a0001 | c0001 | t0041 | g0247 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01433 | hp1 | a0001 | c0001 | t0025 | g0201 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01433 | hp2 | a0001 | c0001 | t0020 | g0004 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01496 | hp1 | a0001 | c0001 | t0048 | g0150 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0192 | AMR | CLM | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01515 | hp1 | a0001 | c0001 | t0043 | g0238 | EUR | IBS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01884 | hp1 | a0001 | c0001 | t0014 | g0191 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01891 | hp2 | a0001 | c0001 | t0080 | g0264 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0235 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0233 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02040 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02055 | hp2 | a0001 | c0001 | t0049 | g0205 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02056 | hp1 | a0001 | c0001 | t0010 | g0018 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02080 | hp1 | a0001 | c0001 | t0022 | g0036 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0170 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | CDX | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | CDX | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0090 | EAS | CDX | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CDX | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02257 | hp1 | a0001 | c0001 | t0014 | g0174 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02257 | hp2 | a0001 | c0001 | t0083 | g0262 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02258 | hp1 | a0001 | c0001 | t0075 | g0280 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02258 | hp2 | a0001 | c0001 | t0018 | g0282 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02273 | hp1 | a0001 | c0001 | t0042 | g0052 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0123 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02280 | hp1 | a0001 | c0001 | t0018 | g0274 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02293 | hp1 | a0001 | c0001 | t0006 | g0119 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0166 | AMR | PEL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02523 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | KHV | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02572 | hp1 | a0001 | c0001 | t0056 | g0141 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02572 | hp2 | a0001 | c0001 | t0071 | g0063 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0185 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02602 | hp2 | a0001 | c0001 | t0015 | g0200 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02615 | hp1 | a0001 | c0001 | t0073 | g0065 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02615 | hp2 | a0001 | c0001 | t0027 | g0269 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0111 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02630 | hp1 | a0001 | c0001 | t0032 | g0285 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02717 | hp1 | a0001 | c0001 | t0074 | g0281 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02717 | hp2 | a0001 | c0001 | t0027 | g0270 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02723 | hp1 | a0001 | c0001 | t0021 | g0221 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02809 | hp1 | a0001 | c0001 | t0019 | g0273 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02809 | hp2 | a0001 | c0001 | t0021 | g0228 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02886 | hp2 | a0001 | c0001 | t0029 | g0266 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02896 | hp2 | a0001 | c0001 | t0013 | g0212 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02922 | hp2 | a0001 | c0001 | t0020 | g0004 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02965 | hp1 | a0001 | c0001 | t0065 | g0120 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02965 | hp2 | a0001 | c0001 | t0072 | g0064 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02970 | hp1 | a0001 | c0001 | t0029 | g0267 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02970 | hp2 | a0001 | c0001 | t0078 | g0263 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03017 | hp1 | a0001 | c0001 | t0060 | g0172 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03017 | hp2 | a0001 | c0001 | t0009 | g0038 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03098 | hp1 | a0001 | c0001 | t0035 | g0220 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03130 | hp1 | a0001 | c0001 | t0089 | g0011 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03130 | hp2 | a0001 | c0001 | t0059 | g0060 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03139 | hp1 | a0001 | c0001 | t0085 | g0213 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03139 | hp2 | a0001 | c0001 | t0013 | g0211 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03195 | hp1 | a0001 | c0001 | t0076 | g0271 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03195 | hp2 | a0001 | c0001 | t0061 | g0086 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0226 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03225 | hp1 | a0001 | c0001 | t0086 | g0210 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0160 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03516 | hp2 | a0001 | c0001 | t0016 | g0062 | AFR | ESN | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03540 | hp1 | a0001 | c0001 | t0028 | g0275 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | GWD | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03669 | hp1 | a0001 | c0001 | t0037 | g0229 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03710 | hp1 | a0001 | c0001 | t0025 | g0202 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04184 | hp1 | a0001 | c0001 | t0069 | g0162 | SAS | BEB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04204 | hp1 | a0001 | c0001 | t0038 | g0041 | SAS | STU | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04204 | hp2 | a0001 | c0001 | t0040 | g0249 | SAS | STU | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04228 | hp1 | a0001 | c0001 | t0050 | g0168 | SAS | STU | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG04228 | hp2 | a0001 | c0001 | t0009 | g0033 | SAS | STU | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18522 | hp1 | a0001 | c0001 | t0079 | g0268 | AFR | YRI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18522 | hp2 | a0001 | c0001 | t0016 | g0066 | AFR | YRI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | CHB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18612 | hp2 | a0001 | c0001 | t0010 | g0016 | EAS | CHB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0176 | EAS | CHB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | CHB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18940 | hp1 | a0001 | c0001 | t0017 | g0147 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18942 | hp1 | a0001 | c0001 | t0045 | g0230 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18942 | hp2 | a0001 | c0001 | t0023 | g0043 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18946 | hp2 | a0001 | c0001 | t0036 | g0215 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18948 | hp1 | a0001 | c0001 | t0014 | g0196 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18948 | hp2 | a0001 | c0001 | t0044 | g0046 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18949 | hp2 | a0001 | c0001 | t0009 | g0250 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18952 | hp1 | a0001 | c0001 | t0068 | g0132 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0088 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18957 | hp2 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18964 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18964 | hp2 | a0001 | c0001 | t0055 | g0177 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18966 | hp2 | a0001 | c0001 | t0057 | g0184 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18967 | hp2 | a0001 | c0001 | t0054 | g0149 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18979 | hp2 | a0001 | c0001 | t0012 | g0013 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18983 | hp2 | a0001 | c0001 | t0023 | g0231 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18985 | hp2 | a0001 | c0001 | t0012 | g0017 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18986 | hp1 | a0001 | c0001 | t0007 | g0113 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18989 | hp2 | a0001 | c0001 | t0017 | g0146 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18991 | hp1 | a0001 | c0001 | t0033 | g0044 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18991 | hp2 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18992 | hp1 | a0001 | c0001 | t0088 | g0010 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18992 | hp2 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18995 | hp2 | a0001 | c0001 | t0030 | g0009 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18998 | hp1 | a0003 | c0004 | t0003 | g0042 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA18998 | hp2 | a0001 | c0001 | t0063 | g0187 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19002 | hp2 | a0001 | c0001 | t0053 | g0186 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19003 | hp1 | a0001 | c0001 | t0015 | g0142 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19003 | hp2 | a0001 | c0001 | t0017 | g0148 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19004 | hp1 | a0001 | c0001 | t0046 | g0050 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19007 | hp2 | a0001 | c0001 | t0024 | g0006 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19011 | hp2 | a0001 | c0001 | t0087 | g0007 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19012 | hp1 | a0001 | c0001 | t0010 | g0020 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19043 | hp1 | a0001 | c0001 | t0082 | g0286 | AFR | LWK | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19043 | hp2 | a0001 | c0001 | t0062 | g0075 | AFR | LWK | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19057 | hp1 | a0001 | c0001 | t0090 | g0012 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19057 | hp2 | a0001 | c0001 | t0067 | g0104 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19058 | hp2 | a0001 | c0001 | t0024 | g0005 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19074 | hp1 | a0001 | c0001 | t0066 | g0171 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19077 | hp1 | a0001 | c0001 | t0070 | g0100 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19080 | hp2 | a0001 | c0001 | t0013 | g0245 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19084 | hp1 | a0001 | c0001 | t0052 | g0058 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19084 | hp2 | a0001 | c0001 | t0030 | g0021 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19087 | hp1 | a0001 | c0001 | t0008 | g0099 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19087 | hp2 | a0001 | c0001 | t0012 | g0014 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0110 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19088 | hp2 | a0001 | c0001 | t0058 | g0059 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19091 | hp2 | a0001 | c0001 | t0015 | g0136 | EAS | JPT | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA19240 | hp2 | a0001 | c0001 | t0028 | g0276 | AFR | YRI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20129 | hp1 | a0001 | c0001 | t0031 | g0284 | AFR | ASW | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20129 | hp2 | a0001 | c0001 | t0051 | g0055 | AFR | ASW | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | TSI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0145 | EUR | TSI | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | GIH | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20905 | hp2 | a0001 | c0001 | t0039 | g0037 | SAS | GIH | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02486 | hp1 | a0001 | c0001 | t0026 | g0278 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02486 | hp2 | a0001 | c0001 | t0016 | g0067 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG02559 | hp2 | a0001 | c0001 | t0019 | g0283 | AFR | ACB | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0208 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG03471 | hp2 | a0001 | c0001 | t0077 | g0265 | AFR | MSL | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG06807 | hp1 | a0001 | c0001 | t0018 | g0277 | AFR | USA | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0260 | AFR | USA | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA20300 | hp2 | a0001 | c0001 | t0034 | g0254 | AFR | USA | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
NA21309 | hp2 | a0001 | c0001 | t0081 | g0023 | AFR | LWK | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
homoSapiens | chm13v2 | a0001 | c0001 | t0084 | g0164 | REF | REF | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0189 | REF | REF | TGFB2_chr1_218340336_218449619 | TGFB2 | chr1 | 218340336 | 218449619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:218346973 | G | A | 1 | a0002 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.272G>A | p.Arg91His | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1638/5868 | 272/1245 | 91/414 | chr1 | 218346973 | |||
chr1:218441262 | C | T | 1 | a0003 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.1145C>T | p.Ser382Phe | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2511/5868 | 1145/1245 | 382/414 | chr1 | 218441262 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:218346815 | G | A | 1 | a0001c0002 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.114G>A | p.Glu38Glu | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1480/5868 | 114/1245 | 38/414 | chr1 | 218346815 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:218345400 | A | G | 7 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0030 others(4): Show |
15 | HG02056.hp1 HG02523.hp2 HG03130.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-1302A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1302 | chr1 | 218345400 | ||||||
chr1:218345472 | G | A | 3 | a0001c0001t0020 a0001c0001t0031 a0001c0001t0032 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-1230G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1230 | chr1 | 218345472 | ||||||
chr1:218345557 | G | C | 1 | a0001c0001t0033 | 1 | NA18991.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1145G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1145 | chr1 | 218345557 | ||||||
chr1:218345686 | C | T | 3 | a0001c0001t0029 a0001c0001t0085 a0001c0001t0086 |
4 | HG02886.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-1016C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 1016 | chr1 | 218345686 | ||||||
chr1:218345956 | G | T | 1 | a0001c0001t0083 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-746G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 746 | chr1 | 218345956 | ||||||
chr1:218345988 | A | C | 27 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0018 others(24): Show |
44 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(41): Show |
5_prime_UTR_variant | MODIFIER | c.-714A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 714 | chr1 | 218345988 | ||||||
chr1:218346025 | T | C | 52 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(49): Show |
132 | HG00438.hp2 HG00738.hp2 HG01109.hp1 others(129): Show |
5_prime_UTR_variant | MODIFIER | c.-677T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 677 | chr1 | 218346025 | ||||||
chr1:218346054 | A | ACG | 5 | a0001c0001t0020 a0001c0001t0031 a0001c0001t0032 others(2): Show |
6 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-646_-645dupGC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 644 | INFO_REALIGN_3_PRIME | chr1 | 218346054 | |||||
chr1:218346056 | G | GCA | 11 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0015 others(8): Show |
21 | HG00741.hp2 HG01243.hp2 HG01433.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-622_-621dupAC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | |||||
chr1:218346056 | G | GCACA | 4 | a0001c0001t0012 a0001c0001t0029 a0001c0001t0034 others(1): Show |
8 | HG02523.hp2 HG02886.hp2 HG02970.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-624_-621dupACAC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | |||||
chr1:218346056 | G | GCACACA | 6 | a0001c0001t0027 a0001c0001t0076 a0001c0001t0078 others(3): Show |
7 | HG02615.hp2 HG02717.hp2 HG02970.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-626_-621dupACACAC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | |||||
chr1:218346056 | G | GCACACAC others(1): Show |
2 | a0001c0001t0018 a0001c0001t0077 |
4 | HG02258.hp2 HG02280.hp1 HG03471.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-628_-621dupACACAC others(2): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | |||||
chr1:218346056 | G | GCACACAC others(3): Show |
3 | a0001c0001t0010 a0001c0001t0028 a0001c0001t0089 |
8 | HG02056.hp1 HG03130.hp1 HG03540.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-630_-621dupACACAC others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | |||||
chr1:218346056 | G | GCACACAC others(5): Show |
4 | a0001c0001t0026 a0001c0001t0030 a0001c0001t0074 others(1): Show |
6 | HG01243.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-632_-621dupACACAC others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | |||||
chr1:218346056 | G | GCACACAC others(11): Show |
1 | a0001c0001t0087 | 1 | NA19011.hp2 | 5_prime_UTR_variant | MODIFIER | c.-638_-621dupACACAC others(12): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | |||||
chr1:218346056 | GCACA | G | 1 | a0001c0001t0017 | 3 | NA18940.hp1 NA18989.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-624_-621delACAC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 621 | INFO_REALIGN_3_PRIME | chr1 | 218346056 | |||||
chr1:218346076 | A | ACACACAC others(5): Show |
1 | a0001c0001t0080 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-621_-620insACGCAC others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | INFO_REALIGN_3_PRIME | chr1 | 218346076 | |||||
chr1:218346081 | C | CACACACA others(6): Show |
1 | a0001c0001t0088 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-621_-620insACACAC others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | chr1 | 218346081 | ||||||
chr1:218346082 | G | A | 2 | a0001c0001t0027 a0001c0001t0076 |
3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
5_prime_UTR_variant | MODIFIER | c.-620G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 620 | chr1 | 218346082 | ||||||
chr1:218346315 | T | C | 1 | a0001c0001t0078 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-387T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 387 | chr1 | 218346315 | ||||||
chr1:218346352 | C | G | 1 | a0001c0001t0046 | 1 | NA19004.hp1 | 5_prime_UTR_variant | MODIFIER | c.-350C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 350 | chr1 | 218346352 | ||||||
chr1:218346414 | A | T | 4 | a0001c0001t0016 a0001c0001t0071 a0001c0001t0072 others(1): Show |
6 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-288A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 288 | chr1 | 218346414 | ||||||
chr1:218346586 | A | AAAAC | 53 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(50): Show |
133 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(130): Show |
5_prime_UTR_variant | MODIFIER | c.-113_-110dupACAA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/7 | 109 | INFO_REALIGN_3_PRIME | chr1 | 218346586 | |||||
chr1:218441401 | G | A | 7 | a0001c0001t0037 a0001c0001t0050 a0001c0001t0051 others(4): Show |
7 | HG03669.hp1 HG04228.hp1 NA18967.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*39G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 39 | chr1 | 218441401 | ||||||
chr1:218441427 | C | T | 1 | a0001c0001t0070 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*65C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 65 | chr1 | 218441427 | ||||||
chr1:218441496 | C | CG | 4 | a0001c0001t0035 a0001c0001t0038 a0001c0001t0056 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*136dupG | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 137 | INFO_REALIGN_3_PRIME | chr1 | 218441496 | |||||
chr1:218441497 | G | A | 1 | a0001c0001t0055 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*135G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 135 | chr1 | 218441497 | ||||||
chr1:218441563 | A | T | 54 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(51): Show |
159 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*201A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 201 | chr1 | 218441563 | ||||||
chr1:218441683 | G | GACAACAA others(2): Show |
4 | a0001c0001t0021 a0001c0001t0049 a0001c0001t0056 others(1): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*335_*343dupCAACAA others(3): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 344 | INFO_REALIGN_3_PRIME | chr1 | 218441683 | |||||
chr1:218442082 | T | C | 1 | a0001c0001t0058 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 720 | chr1 | 218442082 | ||||||
chr1:218442087 | G | C | 2 | a0001c0001t0062 a0001c0001t0071 |
2 | HG02572.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*725G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 725 | chr1 | 218442087 | ||||||
chr1:218442109 | A | C | 64 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(61): Show |
170 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*747A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 747 | chr1 | 218442109 | ||||||
chr1:218442146 | G | A | 1 | a0001c0001t0042 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*784G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 784 | chr1 | 218442146 | ||||||
chr1:218442150 | GT | G | 9 | a0001c0001t0021 a0001c0001t0037 a0001c0001t0049 others(6): Show |
10 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*799delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 799 | INFO_REALIGN_3_PRIME | chr1 | 218442150 | |||||
chr1:218442331 | T | C | 1 | a0001c0001t0075 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*969T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 969 | chr1 | 218442331 | ||||||
chr1:218442343 | C | G | 1 | a0001c0001t0045 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*981C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 981 | chr1 | 218442343 | ||||||
chr1:218442355 | A | G | 1 | a0001c0001t0044 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*993A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 993 | chr1 | 218442355 | ||||||
chr1:218442459 | G | A | 1 | a0001c0001t0039 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1097G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1097 | chr1 | 218442459 | ||||||
chr1:218442490 | G | A | 2 | a0001c0001t0048 a0001c0001t0059 |
2 | HG01496.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1128G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1128 | chr1 | 218442490 | ||||||
chr1:218442583 | G | C | 1 | a0001c0001t0060 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1221 | chr1 | 218442583 | ||||||
chr1:218442672 | C | T | 64 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(61): Show |
170 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1310C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1310 | chr1 | 218442672 | ||||||
chr1:218442677 | T | G | 2 | a0001c0001t0058 a0001c0001t0063 |
2 | NA18998.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1315T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1315 | chr1 | 218442677 | ||||||
chr1:218442751 | C | T | 1 | a0001c0001t0069 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1389 | chr1 | 218442751 | ||||||
chr1:218442805 | T | A | 4 | a0001c0001t0021 a0001c0001t0049 a0001c0001t0056 others(1): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1443T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1443 | chr1 | 218442805 | ||||||
chr1:218442817 | G | A | 1 | a0001c0001t0040 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1455G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1455 | chr1 | 218442817 | ||||||
chr1:218442864 | T | C | 2 | a0001c0001t0043 a0001c0001t0064 |
2 | HG01081.hp2 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1502T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1502 | chr1 | 218442864 | ||||||
chr1:218442890 | A | G | 1 | a0001c0001t0024 | 2 | NA19007.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1528A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1528 | chr1 | 218442890 | ||||||
chr1:218442947 | C | G | 2 | a0001c0001t0008 a0001c0001t0042 |
8 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1585C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1585 | chr1 | 218442947 | ||||||
chr1:218442986 | T | A | 25 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(22): Show |
56 | HG01109.hp2 HG01243.hp1 HG01258.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1624T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1624 | chr1 | 218442986 | ||||||
chr1:218443118 | G | C | 1 | a0001c0001t0050 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1756 | chr1 | 218443118 | ||||||
chr1:218443278 | A | T | 1 | a0001c0001t0068 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1916A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 1916 | chr1 | 218443278 | ||||||
chr1:218443369 | C | T | 1 | a0001c0001t0067 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2007C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2007 | chr1 | 218443369 | ||||||
chr1:218443370 | G | A | 5 | a0001c0001t0006 a0001c0001t0023 a0001c0001t0024 others(2): Show |
14 | HG01258.hp1 HG01496.hp2 HG01928.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2008G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2008 | chr1 | 218443370 | ||||||
chr1:218443550 | T | C | 4 | a0001c0001t0037 a0001c0001t0050 a0001c0001t0051 others(1): Show |
4 | HG03669.hp1 HG04228.hp1 NA19084.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2188T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2188 | chr1 | 218443550 | ||||||
chr1:218443631 | T | C | 1 | a0001c0001t0082 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2269 | chr1 | 218443631 | ||||||
chr1:218443709 | G | GT | 2 | a0001c0001t0005 a0001c0001t0022 |
10 | HG00140.hp1 HG00438.hp2 HG02040.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2361dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2362 | INFO_REALIGN_3_PRIME | chr1 | 218443709 | |||||
chr1:218443709 | GT | G | 22 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(19): Show |
48 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2361delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2361 | INFO_REALIGN_3_PRIME | chr1 | 218443709 | |||||
chr1:218443709 | GTT | G | 42 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(39): Show |
122 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2360_*2361delTT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2360 | INFO_REALIGN_3_PRIME | chr1 | 218443709 | |||||
chr1:218443710 | T | G | 1 | a0001c0001t0001 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2348T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2348 | chr1 | 218443710 | ||||||
chr1:218443793 | C | G | 64 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(61): Show |
170 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*2431C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2431 | chr1 | 218443793 | ||||||
chr1:218443926 | A | G | 2 | a0001c0001t0037 a0001c0001t0052 |
2 | HG03669.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2564A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2564 | chr1 | 218443926 | ||||||
chr1:218444201 | G | A | 58 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(55): Show |
163 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*2839G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2839 | chr1 | 218444201 | ||||||
chr1:218444312 | G | A | 1 | a0001c0001t0058 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2950G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 2950 | chr1 | 218444312 | ||||||
chr1:218444558 | C | T | 58 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(55): Show |
163 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*3196C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 7/7 | 3196 | chr1 | 218444558 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:218347160 | T | C | 2 | a0001c0001t0024g0005 a0001c0001t0024g0006 |
2 | NA19007.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.346+113T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347160 | |||||||
chr1:218347245 | T | G | 15 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(12): Show |
15 | HG02056.hp1 HG02523.hp2 HG03130.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+198T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347245 | |||||||
chr1:218347372 | A | G | 4 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 others(1): Show |
5 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+325A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347372 | |||||||
chr1:218347442 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.346+395G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347442 | |||||||
chr1:218347457 | G | A | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+410G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347457 | |||||||
chr1:218347501 | G | A | 33 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0028 others(30): Show |
33 | HG00738.hp2 HG01175.hp2 HG02004.hp1 others(30): Show |
intron_variant | MODIFIER | c.346+454G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347501 | |||||||
chr1:218347579 | T | C | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+532T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347579 | |||||||
chr1:218347653 | A | G | 131 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0025 others(128): Show |
133 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(130): Show |
intron_variant | MODIFIER | c.346+606A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347653 | |||||||
chr1:218347669 | T | C | 2 | a0001c0001t0004g0209 a0001c0001t0011g0208 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.346+622T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218347669 | |||||||
chr1:218347933 | A | AT | 22 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0003g0053 others(19): Show |
22 | HG00738.hp2 HG01169.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.346+904dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218347933 | ||||||
chr1:218347933 | AT | A | 18 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0004g0209 others(15): Show |
18 | HG00438.hp2 HG02523.hp2 HG02896.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+904delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218347933 | ||||||
chr1:218348080 | A | AAAAG | 8 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0029g0266 others(5): Show |
8 | HG01891.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.346+1049_346+1052d others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218348080 | ||||||
chr1:218348080 | A | G | 12 | a0001c0001t0018g0274 a0001c0001t0018g0277 a0001c0001t0018g0282 others(9): Show |
12 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+1033A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348080 | |||||||
chr1:218348158 | A | G | 3 | a0001c0001t0002g0204 a0001c0001t0007g0203 a0001c0001t0049g0205 |
3 | HG02055.hp1 HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.346+1111A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348158 | |||||||
chr1:218348267 | G | A | 236 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0069 others(233): Show |
238 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.346+1220G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348267 | |||||||
chr1:218348379 | T | C | 1 | a0001c0001t0078g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.346+1332T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348379 | |||||||
chr1:218348522 | C | T | 1 | a0001c0001t0042g0052 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.346+1475C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348522 | |||||||
chr1:218348756 | T | C | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+1709T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348756 | |||||||
chr1:218348939 | A | G | 13 | a0001c0001t0003g0022 a0001c0001t0003g0251 a0001c0001t0003g0253 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+1892A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218348939 | |||||||
chr1:218349126 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0029g0266 a0001c0001t0029g0267 |
3 | HG01891.hp1 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.346+2079C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349126 | |||||||
chr1:218349220 | G | C | 2 | a0001c0001t0029g0266 a0001c0001t0029g0267 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.346+2173G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349220 | |||||||
chr1:218349244 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0007g0160 |
3 | HG02109.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.346+2197G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349244 | |||||||
chr1:218349338 | C | CA | 12 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(9): Show |
12 | HG01109.hp1 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+2299dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218349338 | ||||||
chr1:218349344 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.346+2297A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349344 | |||||||
chr1:218349348 | G | A | 15 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(12): Show |
15 | HG02056.hp1 HG02523.hp2 HG03130.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+2301G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349348 | |||||||
chr1:218349364 | C | A | 1 | a0001c0001t0003g0024 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.346+2317C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349364 | |||||||
chr1:218349683 | A | G | 25 | a0001c0001t0003g0232 a0001c0001t0003g0237 a0001c0001t0003g0239 others(22): Show |
26 | HG00438.hp2 HG00741.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.346+2636A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349683 | |||||||
chr1:218349705 | C | A | 16 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(13): Show |
16 | HG01109.hp1 HG01109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+2658C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349705 | |||||||
chr1:218349857 | G | A | 10 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(7): Show |
10 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.346+2810G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349857 | |||||||
chr1:218349912 | T | G | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+2865T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349912 | |||||||
chr1:218349921 | G | A | 13 | a0001c0001t0018g0274 a0001c0001t0018g0277 a0001c0001t0018g0282 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+2874G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218349921 | |||||||
chr1:218350142 | A | G | 1 | a0001c0001t0004g0051 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.346+3095A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350142 | |||||||
chr1:218350183 | C | T | 15 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(12): Show |
15 | HG02056.hp1 HG02523.hp2 HG03130.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+3136C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350183 | |||||||
chr1:218350184 | G | A | 3 | a0001c0001t0002g0057 a0001c0001t0002g0163 a0001c0001t0069g0162 |
3 | HG03491.hp2 HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.346+3137G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350184 | |||||||
chr1:218350206 | C | G | 3 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0076g0271 |
3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+3159C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350206 | |||||||
chr1:218350308 | G | A | 89 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0025 others(86): Show |
91 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.346+3261G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350308 | |||||||
chr1:218350388 | C | T | 112 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0025 others(109): Show |
114 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(111): Show |
intron_variant | MODIFIER | c.346+3341C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350388 | |||||||
chr1:218350637 | GTTATC | G | 4 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 others(1): Show |
5 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+3594_346+3598d others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218350637 | ||||||
chr1:218350750 | T | C | 1 | a0001c0001t0059g0060 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.346+3703T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350750 | |||||||
chr1:218350962 | A | G | 81 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0025 others(78): Show |
83 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.346+3915A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350962 | |||||||
chr1:218350981 | A | T | 1 | a0001c0001t0083g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346+3934A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218350981 | |||||||
chr1:218351082 | T | C | 3 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 |
3 | HG03225.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.346+4035T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218351082 | |||||||
chr1:218351199 | A | G | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+4152A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218351199 | |||||||
chr1:218351290 | A | G | 238 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0069 others(235): Show |
240 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.346+4243A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218351290 | |||||||
chr1:218351299 | T | C | 34 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0028 others(31): Show |
34 | HG00738.hp2 HG01175.hp2 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.346+4252T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218351299 | |||||||
chr1:218352241 | C | T | 3 | a0001c0001t0015g0200 a0001c0001t0027g0270 a0001c0001t0076g0271 |
3 | HG02602.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+5194C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352241 | |||||||
chr1:218352246 | C | A | 72 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0025 others(69): Show |
73 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.346+5199C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352246 | |||||||
chr1:218352262 | G | A | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+5215G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352262 | |||||||
chr1:218352392 | T | A | 2 | a0001c0001t0085g0213 a0001c0001t0086g0210 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+5345T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352392 | |||||||
chr1:218352684 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+5637T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352684 | |||||||
chr1:218352716 | G | A | 7 | a0001c0001t0016g0062 a0001c0001t0016g0066 a0001c0001t0016g0067 others(4): Show |
7 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+5669G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352716 | |||||||
chr1:218352749 | C | T | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+5702C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352749 | |||||||
chr1:218352886 | G | C | 72 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0025 others(69): Show |
73 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.346+5839G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218352886 | |||||||
chr1:218353369 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.346+6322C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353369 | |||||||
chr1:218353402 | T | G | 1 | a0001c0001t0029g0266 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.346+6355T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353402 | |||||||
chr1:218353471 | T | A | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+6424T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353471 | |||||||
chr1:218353498 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.346+6451A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353498 | |||||||
chr1:218353635 | G | A | 2 | a0001c0001t0021g0221 a0001c0001t0035g0220 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.346+6588G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353635 | |||||||
chr1:218353760 | T | C | 1 | a0001c0001t0080g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+6713T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353760 | |||||||
chr1:218353772 | C | T | 3 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0076g0271 |
3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+6725C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353772 | |||||||
chr1:218353787 | G | A | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+6740G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353787 | |||||||
chr1:218353850 | G | A | 11 | a0001c0001t0004g0209 a0001c0001t0011g0208 a0001c0001t0013g0211 others(8): Show |
11 | HG01243.hp2 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.346+6803G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353850 | |||||||
chr1:218353906 | A | T | 4 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0076g0271 others(1): Show |
4 | HG02615.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+6859A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218353906 | |||||||
chr1:218354045 | A | C | 11 | a0001c0001t0003g0022 a0001c0001t0003g0253 a0001c0001t0003g0255 others(8): Show |
11 | HG01261.hp2 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.346+6998A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354045 | |||||||
chr1:218354191 | A | C | 1 | a0001c0001t0003g0024 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.346+7144A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354191 | |||||||
chr1:218354204 | C | G | 17 | a0001c0001t0001g0061 a0001c0001t0003g0022 a0001c0001t0003g0251 others(14): Show |
17 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+7157C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354204 | |||||||
chr1:218354214 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.346+7167T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354214 | |||||||
chr1:218354225 | G | T | 1 | a0001c0001t0077g0265 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.346+7178G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354225 | |||||||
chr1:218354273 | C | T | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.346+7226C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354273 | |||||||
chr1:218354517 | A | G | 17 | a0001c0001t0001g0061 a0001c0001t0003g0022 a0001c0001t0003g0251 others(14): Show |
17 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+7470A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354517 | |||||||
chr1:218354554 | G | T | 4 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0076g0271 others(1): Show |
4 | HG02615.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+7507G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354554 | |||||||
chr1:218354740 | T | C | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+7693T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354740 | |||||||
chr1:218354745 | G | A | 17 | a0001c0001t0001g0061 a0001c0001t0003g0022 a0001c0001t0003g0251 others(14): Show |
17 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+7698G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354745 | |||||||
chr1:218354892 | A | C | 19 | a0001c0001t0001g0061 a0001c0001t0003g0022 a0001c0001t0003g0251 others(16): Show |
19 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.346+7845A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354892 | |||||||
chr1:218354987 | C | A | 1 | a0001c0001t0002g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.346+7940C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218354987 | |||||||
chr1:218355028 | A | G | 17 | a0001c0001t0001g0061 a0001c0001t0003g0022 a0001c0001t0003g0251 others(14): Show |
17 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+7981A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355028 | |||||||
chr1:218355173 | T | C | 1 | a0001c0001t0002g0071 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.346+8126T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355173 | |||||||
chr1:218355577 | C | T | 21 | a0001c0001t0001g0061 a0001c0001t0003g0022 a0001c0001t0003g0251 others(18): Show |
21 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.346+8530C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355577 | |||||||
chr1:218355582 | G | A | 1 | a0001c0001t0011g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.346+8535G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355582 | |||||||
chr1:218355656 | C | T | 6 | a0001c0001t0004g0209 a0001c0001t0011g0208 a0001c0001t0013g0211 others(3): Show |
6 | HG02809.hp2 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+8609C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355656 | |||||||
chr1:218355838 | A | T | 4 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0076g0271 others(1): Show |
4 | HG02615.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+8791A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355838 | |||||||
chr1:218355903 | A | T | 2 | a0001c0001t0003g0251 a0001c0001t0083g0262 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.346+8856A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355903 | |||||||
chr1:218355938 | A | C | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+8891A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355938 | |||||||
chr1:218355962 | G | A | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+8915G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218355962 | |||||||
chr1:218356000 | T | A | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+8953T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356000 | |||||||
chr1:218356111 | T | C | 2 | a0001c0001t0002g0167 a0001c0001t0008g0166 |
2 | HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.346+9064T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356111 | |||||||
chr1:218356224 | A | T | 1 | a0001c0001t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.346+9177A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356224 | |||||||
chr1:218356244 | G | A | 3 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0076g0271 |
3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+9197G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356244 | |||||||
chr1:218356400 | G | A | 3 | a0001c0001t0005g0072 a0001c0001t0005g0073 a0001c0001t0005g0074 |
3 | NA18964.hp1 NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.346+9353G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356400 | |||||||
chr1:218356425 | T | C | 18 | a0001c0001t0001g0061 a0001c0001t0003g0022 a0001c0001t0003g0251 others(15): Show |
18 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+9378T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356425 | |||||||
chr1:218356519 | G | A | 1 | a0001c0001t0062g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.346+9472G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356519 | |||||||
chr1:218356698 | G | A | 3 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0076g0271 |
3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+9651G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356698 | |||||||
chr1:218356707 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.346+9660C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356707 | |||||||
chr1:218356848 | C | T | 20 | a0001c0001t0004g0209 a0001c0001t0010g0015 a0001c0001t0010g0016 others(17): Show |
20 | HG02056.hp1 HG02523.hp2 HG02809.hp2 others(17): Show |
intron_variant | MODIFIER | c.346+9801C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356848 | |||||||
chr1:218356883 | G | A | 9 | a0001c0001t0018g0274 a0001c0001t0018g0277 a0001c0001t0019g0272 others(6): Show |
9 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.346+9836G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218356883 | |||||||
chr1:218357219 | G | GA | 20 | a0001c0001t0001g0076 a0001c0001t0003g0217 a0001c0001t0003g0218 others(17): Show |
20 | HG01109.hp1 HG01109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.346+10187dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218357219 | ||||||
chr1:218357219 | GA | G | 6 | a0001c0001t0001g0061 a0001c0001t0020g0004 a0001c0001t0029g0267 others(3): Show |
7 | HG01433.hp2 HG01891.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+10187delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218357219 | ||||||
chr1:218357227 | A | G | 11 | a0001c0001t0018g0274 a0001c0001t0018g0277 a0001c0001t0018g0282 others(8): Show |
11 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.346+10180A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357227 | |||||||
chr1:218357305 | G | C | 3 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0076g0271 |
3 | HG02615.hp2 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.346+10258G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357305 | |||||||
chr1:218357416 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.346+10369A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357416 | |||||||
chr1:218357418 | T | A | 3 | a0001c0001t0001g0061 a0001c0001t0029g0267 a0001c0001t0080g0264 |
3 | HG01891.hp2 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.346+10371T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357418 | |||||||
chr1:218357702 | T | G | 13 | a0001c0001t0003g0022 a0001c0001t0003g0251 a0001c0001t0003g0253 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+10655T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357702 | |||||||
chr1:218357820 | A | T | 4 | a0001c0001t0001g0154 a0001c0001t0003g0049 a0001c0001t0004g0048 others(1): Show |
4 | NA18966.hp1 NA19004.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+10773A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357820 | |||||||
chr1:218357842 | G | T | 1 | a0001c0001t0018g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346+10795G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357842 | |||||||
chr1:218357902 | AGTT | A | 5 | a0001c0001t0018g0274 a0001c0001t0018g0277 a0001c0001t0019g0273 others(2): Show |
5 | HG02280.hp1 HG02809.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+10862_346+1086 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218357902 | ||||||
chr1:218357929 | A | G | 5 | a0001c0001t0018g0274 a0001c0001t0018g0277 a0001c0001t0019g0273 others(2): Show |
5 | HG02280.hp1 HG02809.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+10882A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218357929 | |||||||
chr1:218358020 | C | T | 5 | a0001c0001t0018g0274 a0001c0001t0018g0277 a0001c0001t0019g0273 others(2): Show |
5 | HG02280.hp1 HG02809.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+10973C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358020 | |||||||
chr1:218358083 | G | A | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+11036G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358083 | |||||||
chr1:218358426 | T | A | 231 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0076 others(228): Show |
233 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.346+11379T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358426 | |||||||
chr1:218358461 | T | C | 3 | a0001c0001t0026g0278 a0001c0001t0026g0279 a0001c0001t0075g0280 |
3 | HG01243.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+11414T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358461 | |||||||
chr1:218358504 | T | C | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+11457T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358504 | |||||||
chr1:218358548 | C | CT | 40 | a0001c0001t0001g0143 a0001c0001t0002g0157 a0001c0001t0003g0022 others(37): Show |
40 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.346+11519dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218358548 | ||||||
chr1:218358557 | T | C | 1 | a0001c0001t0004g0048 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.346+11510T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358557 | |||||||
chr1:218358572 | A | G | 216 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0076 others(213): Show |
218 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.346+11525A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358572 | |||||||
chr1:218358583 | C | T | 1 | a0001c0001t0080g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+11536C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358583 | |||||||
chr1:218358628 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.346+11581A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358628 | |||||||
chr1:218358641 | G | C | 1 | a0001c0001t0006g0088 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.346+11594G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358641 | |||||||
chr1:218358764 | A | G | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+11717A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358764 | |||||||
chr1:218358790 | C | T | 4 | a0001c0001t0027g0269 a0001c0001t0027g0270 a0001c0001t0076g0271 others(1): Show |
4 | HG02615.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+11743C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358790 | |||||||
chr1:218358799 | C | T | 7 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0002g0204 others(4): Show |
7 | HG02055.hp1 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+11752C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358799 | |||||||
chr1:218358829 | A | G | 8 | a0001c0001t0001g0061 a0001c0001t0018g0274 a0001c0001t0018g0277 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.346+11782A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358829 | |||||||
chr1:218358956 | G | A | 1 | a0001c0001t0004g0048 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.346+11909G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358956 | |||||||
chr1:218358973 | TGGTCAAG others(15): Show |
T | 2 | a0001c0001t0025g0201 a0001c0001t0025g0202 |
2 | HG01433.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.346+11927_346+1194 others(26): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358973 | |||||||
chr1:218358996 | A | T | 2 | a0001c0001t0025g0201 a0001c0001t0025g0202 |
2 | HG01433.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.346+11949A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218358996 | |||||||
chr1:218359116 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.346+12069C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359116 | |||||||
chr1:218359132 | A | T | 1 | a0001c0001t0016g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.346+12085A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359132 | |||||||
chr1:218359181 | G | C | 12 | a0001c0001t0001g0061 a0001c0001t0018g0274 a0001c0001t0018g0277 others(9): Show |
12 | HG01891.hp2 HG02280.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.346+12134G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359181 | |||||||
chr1:218359310 | G | T | 3 | a0001c0001t0026g0278 a0001c0001t0026g0279 a0001c0001t0075g0280 |
3 | HG01243.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+12263G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359310 | |||||||
chr1:218359421 | C | T | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+12374C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359421 | |||||||
chr1:218359430 | C | T | 2 | a0001c0001t0009g0250 a0001c0001t0021g0221 |
2 | HG02723.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.346+12383C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359430 | |||||||
chr1:218359680 | G | T | 5 | a0001c0001t0018g0282 a0001c0001t0019g0283 a0001c0001t0026g0278 others(2): Show |
5 | HG01243.hp1 HG02258.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+12633G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218359680 | |||||||
chr1:218360025 | C | A | 2 | a0001c0001t0077g0265 a0001c0001t0082g0286 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.346+12978C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360025 | |||||||
chr1:218360234 | T | C | 1 | a0001c0001t0021g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.346+13187T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360234 | |||||||
chr1:218360301 | C | T | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+13254C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360301 | |||||||
chr1:218360477 | C | T | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+13430C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360477 | |||||||
chr1:218360478 | G | A | 9 | a0001c0001t0001g0061 a0001c0001t0018g0274 a0001c0001t0018g0277 others(6): Show |
9 | HG01891.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.346+13431G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360478 | |||||||
chr1:218360616 | G | A | 1 | a0001c0001t0025g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.346+13569G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360616 | |||||||
chr1:218360658 | C | T | 18 | a0001c0001t0001g0061 a0001c0001t0003g0251 a0001c0001t0003g0253 others(15): Show |
18 | HG01261.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+13611C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360658 | |||||||
chr1:218360805 | G | A | 4 | a0001c0001t0018g0282 a0001c0001t0019g0283 a0001c0001t0026g0278 others(1): Show |
4 | HG01243.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+13758G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360805 | |||||||
chr1:218360855 | A | AT | 6 | a0001c0001t0004g0047 a0001c0001t0016g0062 a0001c0001t0016g0066 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+13816dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218360855 | ||||||
chr1:218360865 | C | G | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+13818C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360865 | |||||||
chr1:218360957 | C | A | 5 | a0001c0001t0004g0209 a0001c0001t0011g0208 a0001c0001t0013g0211 others(2): Show |
5 | HG02809.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+13910C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218360957 | |||||||
chr1:218361120 | T | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.346+14073T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361120 | |||||||
chr1:218361194 | A | G | 5 | a0001c0001t0003g0227 a0001c0001t0018g0282 a0001c0001t0019g0283 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+14147A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361194 | |||||||
chr1:218361366 | C | A | 1 | a0001c0001t0045g0230 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.346+14319C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361366 | |||||||
chr1:218361461 | C | T | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+14414C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361461 | |||||||
chr1:218361513 | G | A | 1 | a0001c0001t0005g0089 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.346+14466G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361513 | |||||||
chr1:218361636 | C | A | 1 | a0001c0001t0025g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.346+14589C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361636 | |||||||
chr1:218361648 | T | C | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+14601T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361648 | |||||||
chr1:218361817 | G | C | 3 | a0001c0001t0003g0227 a0001c0001t0026g0278 a0001c0001t0026g0279 |
3 | HG01109.hp1 HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+14770G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361817 | |||||||
chr1:218361923 | T | A | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+14876T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361923 | |||||||
chr1:218361950 | G | A | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+14903G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218361950 | |||||||
chr1:218362267 | T | G | 1 | a0001c0001t0003g0025 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.346+15220T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362267 | |||||||
chr1:218362337 | C | T | 17 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(14): Show |
18 | HG01433.hp2 HG02056.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+15290C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362337 | |||||||
chr1:218362423 | C | G | 1 | a0001c0001t0004g0003 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.346+15376C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362423 | |||||||
chr1:218362476 | G | A | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+15429G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362476 | |||||||
chr1:218362573 | A | G | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+15526A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362573 | |||||||
chr1:218362621 | C | A | 1 | a0001c0001t0002g0156 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.346+15574C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362621 | |||||||
chr1:218362712 | C | T | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+15665C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362712 | |||||||
chr1:218362843 | G | T | 1 | a0001c0001t0040g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346+15796G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362843 | |||||||
chr1:218362846 | T | G | 1 | a0001c0001t0040g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346+15799T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362846 | |||||||
chr1:218362861 | A | G | 1 | a0001c0001t0029g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.346+15814A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362861 | |||||||
chr1:218362862 | G | A | 1 | a0001c0001t0040g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346+15815G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218362862 | |||||||
chr1:218363074 | T | C | 1 | a0001c0001t0003g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.346+16027T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363074 | |||||||
chr1:218363501 | G | A | 1 | a0001c0001t0018g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346+16454G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363501 | |||||||
chr1:218363519 | T | C | 1 | a0001c0001t0011g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.346+16472T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363519 | |||||||
chr1:218363580 | A | C | 1 | a0001c0001t0029g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.346+16533A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363580 | |||||||
chr1:218363597 | C | A | 1 | a0001c0001t0005g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.346+16550C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363597 | |||||||
chr1:218363663 | T | C | 2 | a0001c0001t0002g0091 a0001c0001t0015g0142 |
2 | NA18943.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.346+16616T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363663 | |||||||
chr1:218363913 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.346+16866C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363913 | |||||||
chr1:218363947 | G | A | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+16900G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363947 | |||||||
chr1:218363968 | T | C | 128 | a0001c0001t0001g0061 a0001c0001t0001g0093 a0001c0001t0001g0154 others(125): Show |
130 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.346+16921T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218363968 | |||||||
chr1:218364290 | T | C | 2 | a0001c0001t0003g0053 a0001c0001t0003g0054 |
2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.346+17243T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364290 | |||||||
chr1:218364410 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.346+17363G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364410 | |||||||
chr1:218364450 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.346+17403C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364450 | |||||||
chr1:218364480 | C | T | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.346+17433C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364480 | |||||||
chr1:218364517 | A | T | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+17470A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364517 | |||||||
chr1:218364584 | T | C | 1 | a0001c0001t0062g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.346+17537T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364584 | |||||||
chr1:218364719 | A | G | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.346+17672A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364719 | |||||||
chr1:218364754 | A | C | 1 | a0001c0001t0080g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+17707A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364754 | |||||||
chr1:218364786 | A | C | 2 | a0001c0001t0027g0269 a0001c0001t0027g0270 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.346+17739A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364786 | |||||||
chr1:218364791 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+17744G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364791 | |||||||
chr1:218364806 | C | G | 30 | a0001c0001t0001g0061 a0001c0001t0010g0015 a0001c0001t0010g0016 others(27): Show |
31 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.346+17759C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364806 | |||||||
chr1:218364945 | T | C | 1 | a0001c0001t0066g0171 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.346+17898T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218364945 | |||||||
chr1:218365023 | C | G | 3 | a0001c0001t0001g0137 a0001c0001t0002g0135 a0001c0001t0015g0136 |
3 | HG00558.hp1 NA18979.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.346+17976C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365023 | |||||||
chr1:218365096 | C | T | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+18049C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365096 | |||||||
chr1:218365118 | C | T | 19 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(16): Show |
19 | HG02056.hp1 HG02523.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.346+18071C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365118 | |||||||
chr1:218365431 | G | A | 2 | a0001c0001t0026g0278 a0001c0001t0026g0279 |
2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+18384G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365431 | |||||||
chr1:218365664 | A | AT | 34 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0128 others(31): Show |
34 | HG00558.hp1 HG00621.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.346+18632dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218365664 | ||||||
chr1:218365664 | A | ATTTT | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+18629_346+1863 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218365664 | ||||||
chr1:218365664 | AT | A | 12 | a0001c0001t0003g0227 a0001c0001t0004g0209 a0001c0001t0007g0203 others(9): Show |
13 | HG01109.hp1 HG01433.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+18632delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218365664 | ||||||
chr1:218365741 | G | A | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+18694G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365741 | |||||||
chr1:218365898 | G | C | 1 | a0001c0001t0002g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.346+18851G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365898 | |||||||
chr1:218365957 | G | A | 2 | a0001c0001t0026g0278 a0001c0001t0026g0279 |
2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+18910G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218365957 | |||||||
chr1:218366054 | A | G | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+19007A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366054 | |||||||
chr1:218366135 | G | A | 1 | a0001c0001t0080g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+19088G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366135 | |||||||
chr1:218366360 | G | A | 1 | a0001c0001t0060g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.346+19313G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366360 | |||||||
chr1:218366405 | G | C | 18 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(15): Show |
18 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.346+19358G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366405 | |||||||
chr1:218366445 | C | T | 18 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(15): Show |
18 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.346+19398C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366445 | |||||||
chr1:218366483 | A | T | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+19436A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366483 | |||||||
chr1:218366484 | A | T | 1 | a0001c0001t0064g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.346+19437A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366484 | |||||||
chr1:218366615 | G | A | 4 | a0001c0001t0026g0278 a0001c0001t0026g0279 a0001c0001t0027g0269 others(1): Show |
4 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+19568G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366615 | |||||||
chr1:218366715 | G | A | 18 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(15): Show |
18 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.346+19668G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366715 | |||||||
chr1:218366907 | C | T | 1 | a0001c0001t0004g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.346+19860C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218366907 | |||||||
chr1:218367075 | C | A | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+20028C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367075 | |||||||
chr1:218367079 | T | C | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+20032T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367079 | |||||||
chr1:218367113 | G | A | 21 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(18): Show |
21 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.346+20066G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367113 | |||||||
chr1:218367125 | C | T | 18 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(15): Show |
18 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.346+20078C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367125 | |||||||
chr1:218367291 | G | A | 1 | a0001c0001t0025g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.346+20244G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367291 | |||||||
chr1:218367379 | T | C | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.346+20332T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367379 | |||||||
chr1:218367522 | G | A | 2 | a0001c0001t0074g0281 a0001c0001t0085g0213 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.346+20475G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367522 | |||||||
chr1:218367549 | A | G | 13 | a0001c0001t0003g0251 a0001c0001t0003g0253 a0001c0001t0003g0255 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+20502A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367549 | |||||||
chr1:218367792 | AT | A | 4 | a0001c0001t0001g0152 a0001c0001t0017g0146 a0001c0001t0017g0147 others(1): Show |
4 | NA18940.hp1 NA18989.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+20753delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218367792 | ||||||
chr1:218367864 | T | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.346+20817T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367864 | |||||||
chr1:218367891 | C | T | 2 | a0001c0001t0030g0009 a0001c0001t0088g0010 |
2 | NA18992.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.346+20844C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367891 | |||||||
chr1:218367898 | G | A | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+20851G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218367898 | |||||||
chr1:218368365 | A | G | 133 | a0001c0001t0001g0061 a0001c0001t0001g0093 a0001c0001t0001g0154 others(130): Show |
135 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.346+21318A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368365 | |||||||
chr1:218368366 | A | C | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+21319A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368366 | |||||||
chr1:218368647 | T | C | 1 | a0001c0001t0090g0012 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.346+21600T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368647 | |||||||
chr1:218368650 | T | C | 66 | a0001c0001t0001g0093 a0001c0001t0001g0154 a0001c0001t0001g0169 others(63): Show |
67 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.346+21603T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368650 | |||||||
chr1:218368717 | T | G | 133 | a0001c0001t0001g0061 a0001c0001t0001g0093 a0001c0001t0001g0154 others(130): Show |
135 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.346+21670T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368717 | |||||||
chr1:218368724 | GA | G | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+21678delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368724 | |||||||
chr1:218368805 | G | A | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+21758G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368805 | |||||||
chr1:218368943 | A | G | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+21896A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368943 | |||||||
chr1:218368965 | T | C | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+21918T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368965 | |||||||
chr1:218368978 | C | T | 3 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0021g0228 |
3 | HG02809.hp2 HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.346+21931C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218368978 | |||||||
chr1:218369027 | C | T | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+21980C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369027 | |||||||
chr1:218369136 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.346+22089T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369136 | |||||||
chr1:218369181 | G | A | 2 | a0001c0001t0027g0269 a0001c0001t0027g0270 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.346+22134G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369181 | |||||||
chr1:218369250 | G | A | 2 | a0001c0001t0027g0269 a0001c0001t0027g0270 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.346+22203G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369250 | |||||||
chr1:218369256 | G | GA | 42 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0084 others(39): Show |
43 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.346+22246dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | G | GAA | 6 | a0001c0001t0001g0175 a0001c0001t0002g0173 a0001c0001t0005g0072 others(3): Show |
6 | HG02257.hp1 HG03239.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+22245_346+2224 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GA | G | 33 | a0001c0001t0001g0069 a0001c0001t0001g0083 a0001c0001t0001g0085 others(30): Show |
33 | HG00621.hp1 HG01081.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.346+22246delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAA | G | 6 | a0001c0001t0003g0227 a0001c0001t0004g0209 a0001c0001t0011g0208 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+22243_346+2224 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA | G | 17 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(14): Show |
17 | HG02056.hp1 HG02486.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+22240_346+2224 others(11): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA others(1): Show |
G | 12 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(9): Show |
12 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+22239_346+2224 others(12): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA others(2): Show |
G | 17 | a0001c0001t0003g0049 a0001c0001t0003g0232 a0001c0001t0003g0251 others(14): Show |
17 | HG00438.hp2 HG01261.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+22238_346+2224 others(13): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA others(3): Show |
G | 59 | a0001c0001t0001g0093 a0001c0001t0001g0154 a0001c0001t0001g0169 others(56): Show |
60 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.346+22237_346+2224 others(14): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA others(4): Show |
G | 3 | a0001c0001t0003g0246 a0001c0001t0033g0044 a0001c0001t0036g0215 |
3 | NA18943.hp2 NA18946.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.346+22236_346+2224 others(15): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA others(5): Show |
G | 3 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 |
4 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+22235_346+2224 others(16): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA others(7): Show |
G | 2 | a0001c0001t0025g0202 a0001c0001t0049g0205 |
2 | HG02055.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.346+22233_346+2224 others(18): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA others(12): Show |
G | 2 | a0001c0001t0027g0269 a0001c0001t0027g0270 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.346+22228_346+2224 others(23): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA others(13): Show |
G | 4 | a0001c0001t0001g0061 a0001c0001t0018g0277 a0001c0001t0019g0273 others(1): Show |
4 | HG01891.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+22227_346+2224 others(24): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369256 | GAAAAAAA others(14): Show |
G | 2 | a0001c0001t0003g0025 a0001c0001t0079g0268 |
2 | HG03490.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.346+22226_346+2224 others(25): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218369256 | ||||||
chr1:218369262 | A | G | 1 | a0001c0001t0021g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.346+22215A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369262 | |||||||
chr1:218369291 | A | G | 20 | a0001c0001t0003g0227 a0001c0001t0010g0015 a0001c0001t0010g0016 others(17): Show |
20 | HG01109.hp1 HG01243.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.346+22244A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369291 | |||||||
chr1:218369319 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.346+22272A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369319 | |||||||
chr1:218369328 | T | G | 1 | a0001c0001t0021g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.346+22281T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369328 | |||||||
chr1:218369508 | A | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0002g0204 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+22461A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369508 | |||||||
chr1:218369513 | T | G | 3 | a0001c0001t0030g0009 a0001c0001t0087g0007 a0001c0001t0088g0010 |
3 | NA18992.hp1 NA18995.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.346+22466T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369513 | |||||||
chr1:218369534 | C | T | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+22487C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369534 | |||||||
chr1:218369641 | C | T | 2 | a0001c0001t0018g0282 a0001c0001t0019g0283 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.346+22594C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369641 | |||||||
chr1:218369650 | G | A | 1 | a0001c0001t0037g0229 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.346+22603G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369650 | |||||||
chr1:218369670 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.346+22623G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369670 | |||||||
chr1:218369969 | G | T | 16 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(13): Show |
16 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+22922G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218369969 | |||||||
chr1:218370076 | G | A | 1 | a0001c0001t0020g0004 | 2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.346+23029G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370076 | |||||||
chr1:218370689 | C | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0206 a0001c0001t0002g0118 others(3): Show |
6 | HG00642.hp1 HG01175.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+23642C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370689 | |||||||
chr1:218370735 | G | A | 3 | a0001c0001t0003g0227 a0001c0001t0004g0209 a0001c0001t0011g0208 |
3 | HG01109.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.346+23688G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370735 | |||||||
chr1:218370780 | A | T | 1 | a0001c0001t0019g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.346+23733A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370780 | |||||||
chr1:218370876 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.346+23829G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370876 | |||||||
chr1:218370920 | G | A | 1 | a0001c0001t0014g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.346+23873G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218370920 | |||||||
chr1:218371068 | G | A | 24 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(21): Show |
24 | HG01109.hp2 HG01261.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.346+24021G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371068 | |||||||
chr1:218371249 | C | T | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+24202C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371249 | |||||||
chr1:218371309 | C | A | 1 | a0001c0001t0080g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.346+24262C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371309 | |||||||
chr1:218371313 | A | C | 16 | a0001c0001t0004g0026 a0001c0001t0007g0203 a0001c0001t0014g0196 others(13): Show |
16 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+24266A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371313 | |||||||
chr1:218371753 | T | G | 46 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(43): Show |
46 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.346+24706T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371753 | |||||||
chr1:218371835 | A | G | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+24788A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371835 | |||||||
chr1:218371937 | C | T | 1 | a0001c0001t0062g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.346+24890C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218371937 | |||||||
chr1:218372091 | A | C | 1 | a0001c0001t0027g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.346+25044A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372091 | |||||||
chr1:218372391 | G | A | 4 | a0001c0001t0001g0152 a0001c0001t0017g0146 a0001c0001t0017g0147 others(1): Show |
4 | NA18940.hp1 NA18989.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+25344G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372391 | |||||||
chr1:218372427 | T | G | 6 | a0001c0001t0003g0227 a0001c0001t0004g0209 a0001c0001t0011g0208 others(3): Show |
6 | HG01109.hp1 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+25380T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372427 | |||||||
chr1:218372482 | A | G | 1 | a0001c0001t0019g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.346+25435A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372482 | |||||||
chr1:218372828 | A | C | 136 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0069 others(133): Show |
138 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.346+25781A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372828 | |||||||
chr1:218372829 | C | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.346+25782C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372829 | |||||||
chr1:218372848 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0051g0055 a0001c0001t0065g0120 |
3 | HG02886.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.346+25801G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372848 | |||||||
chr1:218372894 | C | T | 15 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(12): Show |
15 | HG02056.hp1 HG02523.hp2 NA18522.hp1 others(12): Show |
intron_variant | MODIFIER | c.346+25847C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218372894 | |||||||
chr1:218373040 | TG | T | 7 | a0001c0001t0001g0061 a0001c0001t0018g0277 a0001c0001t0019g0273 others(4): Show |
7 | HG01891.hp2 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.346+25995delG | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218373040 | ||||||
chr1:218373048 | C | T | 1 | a0001c0001t0005g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.346+26001C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373048 | |||||||
chr1:218373093 | G | A | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+26046G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373093 | |||||||
chr1:218373132 | C | T | 2 | a0001c0001t0018g0274 a0001c0001t0025g0201 |
2 | HG01433.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.346+26085C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373132 | |||||||
chr1:218373149 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+26102C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373149 | |||||||
chr1:218373159 | A | T | 19 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(16): Show |
19 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.346+26112A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373159 | |||||||
chr1:218373266 | G | T | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+26219G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373266 | |||||||
chr1:218373312 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.346+26265A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373312 | |||||||
chr1:218373466 | T | C | 24 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(21): Show |
24 | HG01109.hp2 HG01261.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.346+26419T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373466 | |||||||
chr1:218373613 | G | A | 10 | a0001c0001t0003g0227 a0001c0001t0004g0209 a0001c0001t0011g0208 others(7): Show |
10 | HG01109.hp1 HG02809.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.346+26566G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373613 | |||||||
chr1:218373676 | C | CTA | 10 | a0001c0001t0003g0227 a0001c0001t0004g0209 a0001c0001t0011g0208 others(7): Show |
10 | HG01109.hp1 HG02809.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.346+26631_346+2663 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218373676 | ||||||
chr1:218373739 | T | A | 1 | a0001c0001t0019g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.346+26692T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373739 | |||||||
chr1:218373835 | A | T | 16 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(13): Show |
16 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+26788A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218373835 | |||||||
chr1:218374129 | A | T | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+27082A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374129 | |||||||
chr1:218374156 | T | C | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.346+27109T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374156 | |||||||
chr1:218374265 | G | A | 1 | a0001c0001t0062g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.346+27218G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374265 | |||||||
chr1:218374329 | T | C | 1 | a0001c0001t0007g0170 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.346+27282T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374329 | |||||||
chr1:218374540 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.346+27493C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374540 | |||||||
chr1:218374643 | T | C | 1 | a0001c0001t0031g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.346+27596T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218374643 | |||||||
chr1:218375073 | G | A | 6 | a0001c0001t0001g0061 a0001c0001t0018g0277 a0001c0001t0019g0273 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+28026G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375073 | |||||||
chr1:218375092 | C | T | 1 | a0001c0001t0027g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.346+28045C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375092 | |||||||
chr1:218375179 | C | T | 64 | a0001c0001t0001g0093 a0001c0001t0001g0154 a0001c0001t0001g0169 others(61): Show |
65 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.346+28132C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375179 | |||||||
chr1:218375183 | G | T | 2 | a0001c0001t0003g0244 a0001c0001t0013g0245 |
2 | NA19011.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.346+28136G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375183 | |||||||
chr1:218375184 | G | A | 5 | a0001c0001t0003g0232 a0001c0001t0003g0237 a0001c0001t0004g0235 others(2): Show |
5 | HG01928.hp2 NA18747.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+28137G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375184 | |||||||
chr1:218375382 | G | A | 1 | a0001c0001t0060g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.346+28335G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375382 | |||||||
chr1:218375407 | C | CT | 114 | a0001c0001t0001g0093 a0001c0001t0001g0154 a0001c0001t0001g0169 others(111): Show |
116 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.346+28372dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218375407 | ||||||
chr1:218375438 | T | TA | 73 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0096 others(70): Show |
73 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.346+28403dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218375438 | ||||||
chr1:218375438 | T | TAA | 8 | a0001c0001t0001g0061 a0001c0001t0004g0003 a0001c0001t0018g0277 others(5): Show |
9 | HG01256.hp1 HG01258.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.346+28402_346+2840 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218375438 | ||||||
chr1:218375451 | C | A | 13 | a0001c0001t0001g0061 a0001c0001t0003g0217 a0001c0001t0003g0218 others(10): Show |
13 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+28404C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375451 | |||||||
chr1:218375554 | A | G | 1 | a0001c0001t0060g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.346+28507A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375554 | |||||||
chr1:218375716 | C | T | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+28669C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375716 | |||||||
chr1:218375800 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0175 a0001c0001t0002g0178 others(5): Show |
9 | HG02602.hp1 HG03239.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.346+28753T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375800 | |||||||
chr1:218375863 | G | A | 2 | a0001c0001t0026g0278 a0001c0001t0026g0279 |
2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+28816G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375863 | |||||||
chr1:218375894 | C | T | 5 | a0001c0001t0001g0061 a0001c0001t0018g0277 a0001c0001t0019g0273 others(2): Show |
5 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+28847C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375894 | |||||||
chr1:218375960 | A | C | 1 | a0001c0001t0022g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.346+28913A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218375960 | |||||||
chr1:218376012 | A | T | 64 | a0001c0001t0001g0093 a0001c0001t0001g0154 a0001c0001t0001g0169 others(61): Show |
65 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.346+28965A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376012 | |||||||
chr1:218376015 | G | A | 3 | a0001c0001t0004g0235 a0001c0001t0018g0282 a0001c0001t0019g0283 |
3 | HG01928.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.346+28968G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376015 | |||||||
chr1:218376061 | T | C | 3 | a0001c0001t0003g0227 a0001c0001t0026g0278 a0001c0001t0026g0279 |
3 | HG01109.hp1 HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+29014T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376061 | |||||||
chr1:218376102 | C | T | 6 | a0001c0001t0001g0061 a0001c0001t0018g0277 a0001c0001t0019g0273 others(3): Show |
6 | HG01243.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+29055C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376102 | |||||||
chr1:218376309 | C | T | 1 | a0001c0001t0007g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.347-28860C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376309 | |||||||
chr1:218376361 | A | T | 11 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-28808A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376361 | |||||||
chr1:218376618 | C | T | 2 | a0001c0001t0026g0278 a0001c0001t0026g0279 |
2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.347-28551C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376618 | |||||||
chr1:218376824 | A | T | 1 | a0001c0001t0019g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.347-28345A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376824 | |||||||
chr1:218376868 | A | G | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.347-28301A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376868 | |||||||
chr1:218376919 | G | A | 1 | a0001c0001t0082g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-28250G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218376919 | |||||||
chr1:218377070 | A | AG | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.347-28099_347-2809 others(5): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377070 | |||||||
chr1:218377074 | A | T | 26 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(23): Show |
27 | HG01109.hp2 HG01256.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.347-28095A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377074 | |||||||
chr1:218377144 | C | T | 1 | a0001c0001t0010g0020 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.347-28025C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377144 | |||||||
chr1:218377165 | C | G | 1 | a0001c0001t0002g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.347-28004C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377165 | |||||||
chr1:218377166 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.347-28003G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377166 | |||||||
chr1:218377366 | G | C | 14 | a0001c0001t0010g0015 a0001c0001t0010g0016 a0001c0001t0010g0018 others(11): Show |
14 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.347-27803G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377366 | |||||||
chr1:218377666 | T | G | 52 | a0001c0001t0001g0076 a0001c0001t0001g0097 a0001c0001t0001g0102 others(49): Show |
52 | HG00621.hp1 HG00642.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.347-27503T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377666 | |||||||
chr1:218377681 | C | T | 5 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 others(2): Show |
5 | HG01261.hp2 HG02145.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-27488C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377681 | |||||||
chr1:218377687 | C | T | 13 | a0001c0001t0002g0091 a0001c0001t0010g0015 a0001c0001t0010g0016 others(10): Show |
13 | HG02056.hp1 HG02523.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-27482C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377687 | |||||||
chr1:218377771 | G | C | 10 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0018g0277 others(7): Show |
10 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-27398G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377771 | |||||||
chr1:218377789 | A | G | 1 | a0001c0001t0027g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.347-27380A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377789 | |||||||
chr1:218377856 | C | G | 6 | a0001c0001t0004g0209 a0001c0001t0011g0208 a0001c0001t0020g0004 others(3): Show |
7 | HG01433.hp2 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-27313C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377856 | |||||||
chr1:218377931 | G | A | 10 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0003g0256 others(7): Show |
10 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.347-27238G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377931 | |||||||
chr1:218377955 | AGTGT | A | 4 | a0001c0001t0020g0004 a0001c0001t0031g0284 a0001c0001t0032g0285 others(1): Show |
5 | HG01433.hp2 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-27211_347-2720 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377955 | ||||||
chr1:218377958 | G | GTGTT | 8 | a0001c0001t0002g0094 a0001c0001t0003g0053 a0001c0001t0003g0054 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-27181_347-2717 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377958 | ||||||
chr1:218377958 | GTGTT | G | 34 | a0001c0001t0002g0092 a0001c0001t0002g0135 a0001c0001t0003g0253 others(31): Show |
34 | HG00438.hp1 HG00558.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.347-27181_347-2717 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377958 | ||||||
chr1:218377958 | GTGTTTGT others(1): Show |
G | 9 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0018g0277 others(6): Show |
9 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.347-27185_347-2717 others(12): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377958 | ||||||
chr1:218377958 | GTGTTTGT others(9): Show |
G | 1 | a0001c0001t0015g0142 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.347-27193_347-2717 others(20): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377958 | ||||||
chr1:218377960 | GT | G | 3 | a0001c0001t0074g0281 a0001c0001t0085g0213 a0001c0001t0086g0210 |
3 | HG02717.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.347-27206delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218377960 | ||||||
chr1:218377986 | T | C | 2 | a0001c0001t0018g0282 a0001c0001t0019g0283 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.347-27183T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377986 | |||||||
chr1:218377996 | T | G | 9 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0018g0277 others(6): Show |
9 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.347-27173T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218377996 | |||||||
chr1:218378121 | C | A | 61 | a0001c0001t0001g0093 a0001c0001t0001g0124 a0001c0001t0002g0094 others(58): Show |
62 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.347-27048C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378121 | |||||||
chr1:218378132 | T | A | 1 | a0001c0001t0022g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.347-27037T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378132 | |||||||
chr1:218378148 | G | GATTT | 5 | a0001c0001t0001g0114 a0001c0001t0015g0200 a0001c0001t0025g0202 others(2): Show |
5 | HG02572.hp1 HG02602.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-26983_347-2698 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378148 | ||||||
chr1:218378148 | GATTT | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0117 a0001c0001t0001g0143 others(3): Show |
6 | HG00558.hp1 HG01071.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-26983_347-2698 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378148 | ||||||
chr1:218378148 | GATTTATT others(9): Show |
G | 3 | a0001c0001t0001g0169 a0001c0001t0050g0168 a0002c0003t0002g0080 |
3 | HG00140.hp2 HG00639.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.347-26995_347-2698 others(20): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378148 | ||||||
chr1:218378148 | GATTTATT others(13): Show |
G | 155 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0069 others(152): Show |
156 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.347-26999_347-2698 others(24): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378148 | ||||||
chr1:218378152 | T | G | 1 | a0001c0001t0002g0071 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.347-27017T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378152 | |||||||
chr1:218378159 | TTATTTAT others(11): Show |
T | 4 | a0001c0001t0004g0027 a0001c0001t0023g0043 a0001c0001t0044g0046 others(1): Show |
4 | NA18942.hp2 NA18948.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-27008_347-2699 others(22): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378159 | ||||||
chr1:218378239 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0163 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.347-26930C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378239 | |||||||
chr1:218378245 | T | C | 159 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0069 others(156): Show |
160 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.347-26924T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378245 | |||||||
chr1:218378271 | G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-26898G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378271 | |||||||
chr1:218378297 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.347-26872C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378297 | |||||||
chr1:218378356 | T | C | 47 | a0001c0001t0001g0097 a0001c0001t0001g0109 a0001c0001t0001g0124 others(44): Show |
47 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.347-26813T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378356 | |||||||
chr1:218378384 | C | G | 2 | a0001c0001t0059g0060 a0001c0001t0064g0134 |
2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.347-26785C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378384 | |||||||
chr1:218378385 | C | A | 4 | a0001c0001t0019g0272 a0001c0001t0026g0278 a0001c0001t0028g0275 others(1): Show |
4 | HG01243.hp2 HG02486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-26784C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378385 | |||||||
chr1:218378432 | C | A | 46 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0093 others(43): Show |
46 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.347-26737C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378432 | |||||||
chr1:218378736 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0068 others(114): Show |
120 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.347-26433C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378736 | |||||||
chr1:218378773 | G | GT | 214 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0068 others(211): Show |
218 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.347-26386dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378773 | ||||||
chr1:218378773 | G | GTT | 16 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0003g0232 others(13): Show |
16 | HG01243.hp2 HG01261.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.347-26387_347-2638 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218378773 | ||||||
chr1:218378932 | G | A | 2 | a0001c0001t0074g0281 a0001c0001t0085g0213 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-26237G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378932 | |||||||
chr1:218378945 | T | C | 28 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0159 others(25): Show |
28 | HG01109.hp1 HG01169.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-26224T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378945 | |||||||
chr1:218378948 | C | T | 1 | a0001c0001t0018g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.347-26221C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378948 | |||||||
chr1:218378978 | C | A | 21 | a0001c0001t0001g0061 a0001c0001t0002g0091 a0001c0001t0002g0121 others(18): Show |
21 | HG01109.hp1 HG02055.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.347-26191C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218378978 | |||||||
chr1:218379113 | A | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0068 others(165): Show |
172 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.347-26056A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379113 | |||||||
chr1:218379122 | C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-26047C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379122 | |||||||
chr1:218379126 | C | CT | 3 | a0001c0001t0004g0048 a0001c0001t0008g0099 a0001c0001t0025g0202 |
3 | HG03710.hp1 NA18966.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.347-26040dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379126 | ||||||
chr1:218379126 | C | CTT | 154 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0068 others(151): Show |
158 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.347-26041_347-2604 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379126 | ||||||
chr1:218379126 | C | CTTT | 10 | a0001c0001t0001g0096 a0001c0001t0003g0025 a0001c0001t0005g0073 others(7): Show |
10 | HG00738.hp1 HG02293.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-26042_347-2604 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379126 | ||||||
chr1:218379130 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0068 others(165): Show |
172 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.347-26039C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379130 | |||||||
chr1:218379133 | T | TC | 4 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0007g0160 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-26036_347-2603 others(5): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379133 | |||||||
chr1:218379134 | T | C | 31 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0105 others(28): Show |
31 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.347-26035T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379134 | |||||||
chr1:218379143 | C | T | 2 | a0001c0001t0074g0281 a0001c0001t0085g0213 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-26026C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379143 | |||||||
chr1:218379150 | A | T | 2 | a0001c0001t0074g0281 a0001c0001t0085g0213 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-26019A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379150 | |||||||
chr1:218379169 | G | C | 1 | a0001c0001t0082g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-26000G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379169 | |||||||
chr1:218379172 | A | T | 1 | a0001c0001t0082g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-25997A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379172 | |||||||
chr1:218379187 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.347-25982C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379187 | |||||||
chr1:218379193 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0097 a0001c0001t0001g0102 others(57): Show |
62 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.347-25976T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379193 | |||||||
chr1:218379196 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.347-25973G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379196 | |||||||
chr1:218379201 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0081 others(176): Show |
182 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.347-25968C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379201 | |||||||
chr1:218379213 | A | G | 1 | a0001c0001t0069g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.347-25956A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379213 | |||||||
chr1:218379228 | G | C | 28 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0105 others(25): Show |
28 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-25941G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379228 | |||||||
chr1:218379242 | C | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0085 others(122): Show |
128 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(125): Show |
intron_variant | MODIFIER | c.347-25927C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379242 | |||||||
chr1:218379324 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0094 others(1): Show |
4 | HG00140.hp1 HG01081.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-25845A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379324 | |||||||
chr1:218379383 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(210): Show |
217 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.347-25786C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379383 | |||||||
chr1:218379387 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(210): Show |
217 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.347-25782G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379387 | |||||||
chr1:218379429 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.347-25740C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379429 | |||||||
chr1:218379430 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0003g0029 others(1): Show |
4 | HG02004.hp1 HG02698.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-25739G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379430 | |||||||
chr1:218379487 | C | CTT | 65 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0077 others(62): Show |
67 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.347-25669_347-2566 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379487 | ||||||
chr1:218379487 | C | CTTT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0097 a0001c0001t0001g0102 others(82): Show |
87 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.347-25670_347-2566 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379487 | ||||||
chr1:218379487 | C | CTTTCTT | 15 | a0001c0001t0002g0091 a0001c0001t0002g0121 a0001c0001t0010g0018 others(12): Show |
15 | HG02056.hp1 HG02165.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.347-25679_347-2567 others(10): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379487 | ||||||
chr1:218379487 | C | CTTTT | 29 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0105 others(26): Show |
29 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.347-25671_347-2566 others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218379487 | ||||||
chr1:218379575 | T | C | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347-25594T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379575 | |||||||
chr1:218379629 | T | C | 1 | a0001c0001t0010g0015 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.347-25540T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379629 | |||||||
chr1:218379699 | A | G | 2 | a0001c0001t0002g0115 a0001c0001t0073g0065 |
2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.347-25470A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379699 | |||||||
chr1:218379955 | A | G | 45 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0105 others(42): Show |
45 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.347-25214A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379955 | |||||||
chr1:218379960 | G | A | 3 | a0001c0001t0012g0008 a0001c0001t0012g0013 a0001c0001t0012g0017 |
3 | HG02523.hp2 NA18979.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.347-25209G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379960 | |||||||
chr1:218379965 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.347-25204G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218379965 | |||||||
chr1:218380187 | C | T | 37 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(34): Show |
38 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.347-24982C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380187 | |||||||
chr1:218380201 | C | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0007g0160 |
3 | HG02109.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.347-24968C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380201 | |||||||
chr1:218380222 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.347-24947G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380222 | |||||||
chr1:218380404 | T | G | 1 | a0001c0001t0065g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.347-24765T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380404 | |||||||
chr1:218380526 | T | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-24643T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380526 | |||||||
chr1:218380717 | G | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-24452G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380717 | |||||||
chr1:218380798 | G | A | 1 | a0001c0001t0005g0089 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.347-24371G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380798 | |||||||
chr1:218380884 | C | T | 32 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0087 others(29): Show |
33 | HG01109.hp1 HG01169.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.347-24285C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218380884 | |||||||
chr1:218381075 | T | G | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.347-24094T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381075 | |||||||
chr1:218381091 | C | G | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347-24078C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381091 | |||||||
chr1:218381149 | C | T | 2 | a0001c0001t0014g0174 a0001c0001t0014g0191 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.347-24020C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381149 | |||||||
chr1:218381252 | G | T | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-23917G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381252 | |||||||
chr1:218381258 | G | GT | 114 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0093 others(111): Show |
115 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.347-23896dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381258 | ||||||
chr1:218381258 | G | GTT | 11 | a0001c0001t0002g0179 a0001c0001t0003g0217 a0001c0001t0003g0227 others(8): Show |
11 | HG01109.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.347-23897_347-2389 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381258 | ||||||
chr1:218381258 | G | T | 2 | a0001c0001t0002g0127 a0001c0001t0027g0269 |
2 | HG02615.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.347-23911G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381258 | |||||||
chr1:218381263 | T | TG | 2 | a0001c0001t0001g0001 a0001c0001t0003g0045 |
3 | HG02056.hp2 NA18974.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.347-23906_347-2390 others(5): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381263 | |||||||
chr1:218381282 | G | C | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347-23887G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381282 | |||||||
chr1:218381290 | CTG | C | 5 | a0001c0001t0019g0272 a0001c0001t0026g0278 a0001c0001t0028g0275 others(2): Show |
5 | HG01243.hp2 HG02486.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-23877_347-2387 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381290 | ||||||
chr1:218381444 | C | T | 15 | a0001c0001t0002g0091 a0001c0001t0002g0121 a0001c0001t0010g0018 others(12): Show |
15 | HG02056.hp1 HG02165.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.347-23725C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381444 | |||||||
chr1:218381490 | G | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0097 others(75): Show |
80 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.347-23679G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381490 | |||||||
chr1:218381501 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.347-23668G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381501 | |||||||
chr1:218381832 | G | GGT | 10 | a0001c0001t0003g0253 a0001c0001t0007g0111 a0001c0001t0018g0277 others(7): Show |
10 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-23321_347-2332 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381832 | ||||||
chr1:218381832 | G | T | 1 | a0001c0001t0003g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-23337G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381832 | |||||||
chr1:218381832 | GGT | G | 4 | a0001c0001t0001g0085 a0001c0001t0001g0096 a0001c0001t0074g0281 others(1): Show |
4 | HG00738.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-23321_347-2332 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218381832 | ||||||
chr1:218381851 | A | T | 3 | a0001c0001t0001g0103 a0001c0001t0051g0055 a0001c0001t0065g0120 |
3 | HG02886.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-23318A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381851 | |||||||
chr1:218381859 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0007g0160 |
3 | HG02109.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.347-23310G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381859 | |||||||
chr1:218381992 | T | C | 1 | a0001c0001t0010g0018 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.347-23177T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218381992 | |||||||
chr1:218382009 | G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-23160G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382009 | |||||||
chr1:218382013 | C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-23156C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382013 | |||||||
chr1:218382175 | C | T | 5 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0003g0253 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-22994C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382175 | |||||||
chr1:218382250 | C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-22919C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382250 | |||||||
chr1:218382358 | G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-22811G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382358 | |||||||
chr1:218382694 | T | C | 38 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0093 others(35): Show |
38 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.347-22475T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382694 | |||||||
chr1:218382752 | G | A | 6 | a0001c0001t0001g0061 a0001c0001t0001g0159 a0001c0001t0001g0161 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-22417G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382752 | |||||||
chr1:218382860 | C | T | 106 | a0001c0001t0001g0061 a0001c0001t0001g0077 a0001c0001t0001g0081 others(103): Show |
107 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.347-22309C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382860 | |||||||
chr1:218382863 | G | A | 1 | a0001c0001t0035g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.347-22306G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382863 | |||||||
chr1:218382955 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.347-22214T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382955 | |||||||
chr1:218382980 | G | T | 1 | a0001c0001t0042g0052 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.347-22189G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218382980 | |||||||
chr1:218383349 | C | A | 2 | a0001c0001t0074g0281 a0001c0001t0085g0213 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-21820C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383349 | |||||||
chr1:218383377 | CT | C | 7 | a0001c0001t0004g0224 a0001c0001t0007g0111 a0001c0001t0009g0222 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.347-21787delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218383377 | ||||||
chr1:218383492 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.347-21677C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383492 | |||||||
chr1:218383532 | G | T | 1 | a0001c0001t0003g0255 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.347-21637G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383532 | |||||||
chr1:218383658 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0007g0160 |
3 | HG02109.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.347-21511C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383658 | |||||||
chr1:218383703 | C | T | 4 | a0001c0001t0004g0252 a0001c0001t0018g0277 a0001c0001t0026g0279 others(1): Show |
4 | HG01243.hp1 HG02647.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-21466C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383703 | |||||||
chr1:218383937 | G | T | 13 | a0001c0001t0002g0091 a0001c0001t0010g0018 a0001c0001t0010g0019 others(10): Show |
13 | HG02056.hp1 HG02523.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-21232G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383937 | |||||||
chr1:218383968 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0073g0065 |
2 | HG01256.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.347-21201G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383968 | |||||||
chr1:218383988 | T | G | 1 | a0001c0001t0082g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-21181T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218383988 | |||||||
chr1:218384123 | GA | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(153): Show |
160 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.347-21035delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218384123 | ||||||
chr1:218384175 | G | A | 11 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0161 others(8): Show |
11 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.347-20994G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384175 | |||||||
chr1:218384267 | T | C | 33 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0106 others(30): Show |
33 | HG00438.hp1 HG00738.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.347-20902T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384267 | |||||||
chr1:218384313 | C | T | 13 | a0001c0001t0002g0091 a0001c0001t0010g0018 a0001c0001t0010g0019 others(10): Show |
13 | HG02056.hp1 HG02523.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-20856C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384313 | |||||||
chr1:218384314 | G | A | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-20855G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384314 | |||||||
chr1:218384320 | AGG | A | 5 | a0001c0001t0004g0224 a0001c0001t0009g0222 a0001c0001t0011g0225 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-20848_347-2084 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384320 | |||||||
chr1:218384401 | A | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0243 |
2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.347-20768A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384401 | |||||||
chr1:218384419 | T | A | 2 | a0001c0001t0001g0116 a0001c0001t0073g0065 |
2 | HG01256.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.347-20750T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384419 | |||||||
chr1:218384470 | G | A | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-20699G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384470 | |||||||
chr1:218384565 | C | T | 7 | a0001c0001t0004g0224 a0001c0001t0007g0111 a0001c0001t0009g0222 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.347-20604C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384565 | |||||||
chr1:218384578 | G | T | 7 | a0001c0001t0004g0224 a0001c0001t0007g0111 a0001c0001t0009g0222 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.347-20591G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384578 | |||||||
chr1:218384644 | T | C | 3 | a0001c0001t0004g0252 a0001c0001t0026g0279 a0001c0001t0079g0268 |
3 | HG01243.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.347-20525T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384644 | |||||||
chr1:218384737 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0002g0095 |
2 | HG00621.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.347-20432T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384737 | |||||||
chr1:218384843 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.347-20326G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384843 | |||||||
chr1:218384985 | C | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(99): Show |
105 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.347-20184C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218384985 | |||||||
chr1:218385036 | C | G | 1 | a0001c0001t0002g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.347-20133C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385036 | |||||||
chr1:218385097 | G | A | 1 | a0001c0001t0007g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.347-20072G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385097 | |||||||
chr1:218385103 | A | G | 33 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0106 others(30): Show |
33 | HG00438.hp1 HG00738.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.347-20066A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385103 | |||||||
chr1:218385113 | CCT | C | 7 | a0001c0001t0001g0077 a0001c0001t0003g0218 a0001c0001t0003g0219 others(4): Show |
7 | HG01169.hp1 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-20051_347-2005 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218385113 | ||||||
chr1:218385116 | C | T | 7 | a0001c0001t0004g0224 a0001c0001t0007g0111 a0001c0001t0009g0222 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.347-20053C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385116 | |||||||
chr1:218385189 | A | C | 7 | a0001c0001t0004g0224 a0001c0001t0007g0111 a0001c0001t0009g0222 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.347-19980A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385189 | |||||||
chr1:218385246 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(149): Show |
155 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.347-19923G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385246 | |||||||
chr1:218385343 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.347-19826T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385343 | |||||||
chr1:218385369 | C | T | 2 | a0001c0001t0074g0281 a0001c0001t0085g0213 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.347-19800C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385369 | |||||||
chr1:218385411 | C | T | 3 | a0001c0001t0003g0025 a0001c0001t0018g0277 a0001c0001t0075g0280 |
3 | HG02258.hp1 HG03490.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.347-19758C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385411 | |||||||
chr1:218385553 | C | A | 3 | a0001c0001t0004g0252 a0001c0001t0026g0279 a0001c0001t0079g0268 |
3 | HG01243.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.347-19616C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385553 | |||||||
chr1:218385634 | T | C | 3 | a0001c0001t0001g0103 a0001c0001t0051g0055 a0001c0001t0065g0120 |
3 | HG02886.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-19535T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385634 | |||||||
chr1:218385690 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(107): Show |
113 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.347-19479G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385690 | |||||||
chr1:218385752 | T | C | 1 | a0001c0001t0033g0044 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.347-19417T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385752 | |||||||
chr1:218385938 | A | G | 58 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0106 others(55): Show |
59 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.347-19231A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218385938 | |||||||
chr1:218386017 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.347-19152G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386017 | |||||||
chr1:218386071 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0002g0135 a0001c0001t0015g0136 |
3 | HG00558.hp1 NA18979.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.347-19098G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386071 | |||||||
chr1:218386133 | C | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(108): Show |
114 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.347-19036C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386133 | |||||||
chr1:218386198 | G | C | 3 | a0001c0001t0001g0103 a0001c0001t0051g0055 a0001c0001t0065g0120 |
3 | HG02886.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-18971G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386198 | |||||||
chr1:218386269 | G | A | 13 | a0001c0001t0002g0091 a0001c0001t0010g0018 a0001c0001t0010g0019 others(10): Show |
13 | HG02056.hp1 HG02523.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-18900G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386269 | |||||||
chr1:218386533 | T | C | 7 | a0001c0001t0004g0224 a0001c0001t0007g0111 a0001c0001t0009g0222 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.347-18636T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386533 | |||||||
chr1:218386567 | T | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0116 a0001c0001t0026g0278 others(3): Show |
6 | HG01256.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-18602T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386567 | |||||||
chr1:218386664 | G | A | 2 | a0001c0001t0020g0004 a0001c0001t0031g0284 |
3 | HG01433.hp2 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.347-18505G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386664 | |||||||
chr1:218386823 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(106): Show |
112 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.347-18346C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386823 | |||||||
chr1:218386888 | G | A | 6 | a0001c0001t0001g0087 a0001c0001t0001g0116 a0001c0001t0026g0278 others(3): Show |
6 | HG01256.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-18281G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386888 | |||||||
chr1:218386998 | C | T | 1 | a0001c0001t0019g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.347-18171C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218386998 | |||||||
chr1:218387115 | G | T | 1 | a0001c0001t0002g0156 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.347-18054G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387115 | |||||||
chr1:218387311 | A | G | 7 | a0001c0001t0001g0077 a0001c0001t0003g0218 a0001c0001t0003g0219 others(4): Show |
7 | HG01169.hp1 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-17858A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387311 | |||||||
chr1:218387347 | A | C | 1 | a0001c0001t0066g0171 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.347-17822A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387347 | |||||||
chr1:218387398 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.347-17771G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387398 | |||||||
chr1:218387598 | G | T | 1 | a0001c0001t0072g0064 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.347-17571G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387598 | |||||||
chr1:218387620 | G | GA | 9 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0003g0227 others(6): Show |
9 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.347-17548dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218387620 | ||||||
chr1:218387630 | G | C | 3 | a0001c0001t0001g0103 a0001c0001t0026g0278 a0001c0001t0082g0286 |
3 | HG02486.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.347-17539G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387630 | |||||||
chr1:218387690 | T | C | 1 | a0001c0001t0004g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.347-17479T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387690 | |||||||
chr1:218387834 | A | G | 4 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0007g0160 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-17335A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387834 | |||||||
chr1:218387944 | C | G | 6 | a0001c0001t0003g0253 a0001c0001t0004g0252 a0001c0001t0018g0274 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-17225C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387944 | |||||||
chr1:218387959 | C | T | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.347-17210C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218387959 | |||||||
chr1:218388075 | T | G | 1 | a0002c0003t0002g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.347-17094T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388075 | |||||||
chr1:218388102 | A | C | 1 | a0001c0001t0011g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.347-17067A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388102 | |||||||
chr1:218388239 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0077 others(121): Show |
125 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.347-16930C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388239 | |||||||
chr1:218388327 | GC | G | 18 | a0001c0001t0001g0143 a0001c0001t0002g0112 a0001c0001t0002g0195 others(15): Show |
18 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.347-16835delC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218388327 | ||||||
chr1:218388330 | C | T | 1 | a0001c0001t0019g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.347-16839C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388330 | |||||||
chr1:218388432 | GACA | G | 13 | a0001c0001t0001g0061 a0001c0001t0001g0077 a0001c0001t0001g0103 others(10): Show |
13 | HG01169.hp1 HG01884.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-16733_347-1673 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218388432 | ||||||
chr1:218388446 | G | A | 1 | a0001c0001t0029g0266 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.347-16723G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388446 | |||||||
chr1:218388631 | G | A | 1 | a0001c0001t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.347-16538G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388631 | |||||||
chr1:218388638 | G | A | 1 | a0001c0001t0025g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.347-16531G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218388638 | |||||||
chr1:218389011 | C | T | 1 | a0001c0001t0062g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.347-16158C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389011 | |||||||
chr1:218389179 | T | C | 1 | a0001c0001t0006g0192 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.347-15990T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389179 | |||||||
chr1:218389199 | C | A | 21 | a0001c0001t0001g0087 a0001c0001t0001g0103 a0001c0001t0004g0223 others(18): Show |
21 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.347-15970C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389199 | |||||||
chr1:218389297 | G | A | 1 | a0001c0001t0003g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347-15872G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389297 | |||||||
chr1:218389366 | C | T | 27 | a0001c0001t0006g0088 a0001c0001t0006g0119 a0001c0001t0006g0123 others(24): Show |
27 | HG01261.hp1 HG01346.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.347-15803C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389366 | |||||||
chr1:218389497 | T | A | 5 | a0001c0001t0007g0111 a0001c0001t0007g0160 a0001c0001t0014g0174 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-15672T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389497 | |||||||
chr1:218389526 | C | T | 31 | a0001c0001t0006g0088 a0001c0001t0006g0119 a0001c0001t0006g0123 others(28): Show |
31 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.347-15643C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389526 | |||||||
chr1:218389581 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0002g0204 a0001c0001t0029g0266 |
3 | HG02622.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.347-15588A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389581 | |||||||
chr1:218389694 | C | T | 75 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0001g0103 others(72): Show |
75 | HG01109.hp2 HG01169.hp1 HG01243.hp2 others(72): Show |
intron_variant | MODIFIER | c.347-15475C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389694 | |||||||
chr1:218389884 | C | G | 1 | a0001c0001t0056g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.347-15285C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389884 | |||||||
chr1:218389973 | A | C | 1 | a0001c0001t0003g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-15196A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218389973 | |||||||
chr1:218390335 | C | T | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-14834C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390335 | |||||||
chr1:218390350 | AC | A | 3 | a0001c0001t0002g0056 a0001c0001t0002g0129 a0001c0001t0004g0047 |
3 | NA18974.hp2 NA18995.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.347-14818delC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390350 | |||||||
chr1:218390351 | C | A | 78 | a0001c0001t0002g0057 a0001c0001t0002g0092 a0001c0001t0002g0095 others(75): Show |
80 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.347-14818C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390351 | |||||||
chr1:218390467 | T | C | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.347-14702T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390467 | |||||||
chr1:218390486 | G | A | 1 | a0001c0001t0015g0136 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.347-14683G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390486 | |||||||
chr1:218390791 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.347-14378C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218390791 | |||||||
chr1:218391010 | T | C | 3 | a0001c0001t0003g0227 a0001c0001t0028g0275 a0001c0001t0028g0276 |
3 | HG01109.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-14159T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391010 | |||||||
chr1:218391155 | G | A | 1 | a0001c0001t0010g0020 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.347-14014G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391155 | |||||||
chr1:218391302 | C | T | 69 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(66): Show |
69 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(66): Show |
intron_variant | MODIFIER | c.347-13867C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391302 | |||||||
chr1:218391340 | C | T | 1 | a0001c0001t0036g0215 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.347-13829C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391340 | |||||||
chr1:218391431 | G | A | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-13738G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391431 | |||||||
chr1:218391521 | C | T | 1 | a0001c0001t0015g0200 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.347-13648C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391521 | |||||||
chr1:218391539 | C | T | 147 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(144): Show |
149 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.347-13630C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391539 | |||||||
chr1:218391553 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.347-13616C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391553 | |||||||
chr1:218391628 | C | G | 132 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(129): Show |
132 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(129): Show |
intron_variant | MODIFIER | c.347-13541C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391628 | |||||||
chr1:218391635 | T | C | 69 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(66): Show |
69 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(66): Show |
intron_variant | MODIFIER | c.347-13534T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391635 | |||||||
chr1:218391641 | A | C | 1 | a0001c0001t0038g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.347-13528A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391641 | |||||||
chr1:218391959 | G | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-13210G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391959 | |||||||
chr1:218391982 | G | A | 138 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(135): Show |
140 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.347-13187G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218391982 | |||||||
chr1:218392070 | G | A | 13 | a0001c0001t0001g0087 a0001c0001t0004g0223 a0001c0001t0004g0224 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-13099G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392070 | |||||||
chr1:218392080 | G | A | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-13089G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392080 | |||||||
chr1:218392103 | G | A | 1 | a0001c0001t0007g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.347-13066G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392103 | |||||||
chr1:218392168 | G | A | 21 | a0001c0001t0001g0087 a0001c0001t0003g0255 a0001c0001t0004g0223 others(18): Show |
21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.347-13001G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392168 | |||||||
chr1:218392301 | C | T | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347-12868C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392301 | |||||||
chr1:218392364 | A | T | 1 | a0001c0001t0004g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.347-12805A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392364 | |||||||
chr1:218392595 | C | CTGTCT | 10 | a0001c0001t0002g0091 a0001c0001t0002g0173 a0001c0001t0004g0030 others(7): Show |
10 | HG02074.hp1 NA18943.hp1 NA18986.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-12560_347-1255 others(9): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218392595 | ||||||
chr1:218392805 | C | A | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.347-12364C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392805 | |||||||
chr1:218392823 | T | G | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-12346T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392823 | |||||||
chr1:218392900 | G | A | 1 | a0001c0001t0011g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.347-12269G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392900 | |||||||
chr1:218392908 | T | C | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-12261T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218392908 | |||||||
chr1:218393206 | C | T | 13 | a0001c0001t0001g0087 a0001c0001t0004g0223 a0001c0001t0004g0224 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-11963C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393206 | |||||||
chr1:218393269 | A | G | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.347-11900A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393269 | |||||||
chr1:218393297 | A | G | 2 | a0001c0001t0007g0203 a0001c0001t0086g0210 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.347-11872A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393297 | |||||||
chr1:218393513 | A | G | 1 | a0001c0001t0003g0255 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.347-11656A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393513 | |||||||
chr1:218393536 | T | G | 44 | a0001c0001t0001g0077 a0001c0001t0003g0218 a0001c0001t0003g0219 others(41): Show |
44 | HG01169.hp1 HG01261.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.347-11633T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393536 | |||||||
chr1:218393598 | C | G | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-11571C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393598 | |||||||
chr1:218393767 | C | G | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-11402C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393767 | |||||||
chr1:218393999 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.347-11170C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218393999 | |||||||
chr1:218394100 | G | A | 6 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0105 others(3): Show |
6 | HG00738.hp1 HG02004.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-11069G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394100 | |||||||
chr1:218394152 | G | A | 150 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(147): Show |
152 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.347-11017G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394152 | |||||||
chr1:218394209 | G | A | 3 | a0001c0001t0004g0252 a0001c0001t0073g0065 a0001c0001t0079g0268 |
3 | HG02615.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.347-10960G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394209 | |||||||
chr1:218394289 | C | T | 13 | a0001c0001t0001g0087 a0001c0001t0004g0223 a0001c0001t0004g0224 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-10880C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394289 | |||||||
chr1:218394306 | A | T | 10 | a0001c0001t0002g0091 a0001c0001t0002g0173 a0001c0001t0004g0030 others(7): Show |
10 | HG02074.hp1 NA18943.hp1 NA18986.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-10863A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394306 | |||||||
chr1:218394634 | G | A | 1 | a0001c0001t0029g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.347-10535G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218394634 | |||||||
chr1:218395017 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0083 a0001c0001t0001g0140 others(19): Show |
23 | HG00140.hp1 HG00438.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.347-10152G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395017 | |||||||
chr1:218395131 | G | A | 66 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(63): Show |
66 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.347-10038G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395131 | |||||||
chr1:218395140 | T | A | 68 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(65): Show |
68 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.347-10029T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395140 | |||||||
chr1:218395197 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0181 |
2 | NA18979.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.347-9972G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395197 | |||||||
chr1:218395428 | C | T | 1 | a0001c0001t0003g0029 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.347-9741C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395428 | |||||||
chr1:218395462 | G | A | 66 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(63): Show |
66 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.347-9707G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395462 | |||||||
chr1:218395487 | A | G | 133 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(130): Show |
133 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(130): Show |
intron_variant | MODIFIER | c.347-9682A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395487 | |||||||
chr1:218395564 | A | G | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.347-9605A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395564 | |||||||
chr1:218395611 | C | CT | 55 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0085 others(52): Show |
55 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.347-9543dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218395611 | ||||||
chr1:218395611 | CT | C | 20 | a0001c0001t0001g0087 a0001c0001t0003g0255 a0001c0001t0004g0223 others(17): Show |
20 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.347-9543delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218395611 | ||||||
chr1:218395618 | T | C | 1 | a0001c0001t0004g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.347-9551T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395618 | |||||||
chr1:218395646 | C | T | 1 | a0001c0001t0003g0242 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.347-9523C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395646 | |||||||
chr1:218395685 | C | A | 49 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0085 others(46): Show |
49 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.347-9484C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395685 | |||||||
chr1:218395772 | T | C | 66 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(63): Show |
66 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.347-9397T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395772 | |||||||
chr1:218395816 | A | G | 2 | a0001c0001t0005g0089 a0001c0001t0005g0145 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.347-9353A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395816 | |||||||
chr1:218395836 | G | T | 1 | a0001c0001t0010g0020 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.347-9333G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395836 | |||||||
chr1:218395866 | G | A | 66 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(63): Show |
66 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.347-9303G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395866 | |||||||
chr1:218395883 | G | A | 1 | a0001c0001t0034g0254 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.347-9286G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395883 | |||||||
chr1:218395905 | C | T | 30 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0096 others(27): Show |
30 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.347-9264C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395905 | |||||||
chr1:218395999 | A | G | 1 | a0001c0001t0006g0192 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.347-9170A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218395999 | |||||||
chr1:218396128 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-9041C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396128 | |||||||
chr1:218396151 | C | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-9018C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396151 | |||||||
chr1:218396308 | GTGGAATT others(9): Show |
G | 1 | a0001c0001t0024g0005 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.347-8860_347-8845d others(18): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396308 | |||||||
chr1:218396349 | G | T | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-8820G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396349 | |||||||
chr1:218396541 | CTT | C | 13 | a0001c0001t0001g0087 a0001c0001t0004g0223 a0001c0001t0004g0224 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-8617_347-8616d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218396541 | ||||||
chr1:218396762 | C | G | 1 | a0001c0001t0020g0004 | 2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.347-8407C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396762 | |||||||
chr1:218396834 | C | T | 28 | a0001c0001t0006g0088 a0001c0001t0006g0119 a0001c0001t0006g0123 others(25): Show |
28 | HG01261.hp1 HG01346.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-8335C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396834 | |||||||
chr1:218396989 | C | T | 45 | a0001c0001t0001g0077 a0001c0001t0003g0218 a0001c0001t0003g0219 others(42): Show |
45 | HG01169.hp1 HG01261.hp1 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.347-8180C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218396989 | |||||||
chr1:218397128 | C | G | 5 | a0001c0001t0001g0061 a0001c0001t0001g0103 a0001c0001t0001g0158 others(2): Show |
5 | HG01891.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-8041C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397128 | |||||||
chr1:218397161 | A | C | 1 | a0001c0001t0004g0003 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.347-8008A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397161 | |||||||
chr1:218397185 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.347-7984G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397185 | |||||||
chr1:218397266 | T | TA | 13 | a0001c0001t0001g0128 a0001c0001t0002g0091 a0001c0001t0002g0173 others(10): Show |
13 | HG02056.hp1 HG02074.hp1 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.347-7888dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397266 | ||||||
chr1:218397266 | T | TAA | 43 | a0001c0001t0001g0077 a0001c0001t0003g0218 a0001c0001t0003g0219 others(40): Show |
43 | HG01169.hp1 HG01261.hp1 HG01261.hp2 others(40): Show |
intron_variant | MODIFIER | c.347-7889_347-7888d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397266 | ||||||
chr1:218397266 | TA | T | 21 | a0001c0001t0001g0087 a0001c0001t0003g0255 a0001c0001t0004g0223 others(18): Show |
21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.347-7888delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397266 | ||||||
chr1:218397290 | G | A | 13 | a0001c0001t0001g0087 a0001c0001t0004g0223 a0001c0001t0004g0224 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-7879G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397290 | |||||||
chr1:218397301 | T | G | 73 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(70): Show |
74 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.347-7868T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397301 | |||||||
chr1:218397421 | G | C | 6 | a0001c0001t0007g0111 a0001c0001t0007g0160 a0001c0001t0014g0174 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-7748G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397421 | |||||||
chr1:218397561 | C | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-7608C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397561 | |||||||
chr1:218397563 | C | CA | 9 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0002g0115 others(6): Show |
9 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.347-7587dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397563 | ||||||
chr1:218397563 | C | CAA | 52 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(49): Show |
52 | HG01109.hp2 HG01169.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.347-7588_347-7587d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397563 | ||||||
chr1:218397563 | CA | C | 87 | a0001c0001t0001g0061 a0001c0001t0001g0103 a0001c0001t0001g0158 others(84): Show |
88 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.347-7587delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218397563 | ||||||
chr1:218397583 | G | A | 8 | a0001c0001t0004g0224 a0001c0001t0004g0252 a0001c0001t0011g0225 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-7586G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397583 | |||||||
chr1:218397645 | T | C | 1 | a0001c0001t0082g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-7524T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397645 | |||||||
chr1:218397724 | A | G | 68 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(65): Show |
68 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.347-7445A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397724 | |||||||
chr1:218397738 | T | C | 1 | a0001c0001t0052g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.347-7431T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397738 | |||||||
chr1:218397903 | G | A | 1 | a0001c0001t0050g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.347-7266G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397903 | |||||||
chr1:218397972 | C | G | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-7197C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218397972 | |||||||
chr1:218398051 | A | G | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-7118A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398051 | |||||||
chr1:218398219 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.347-6950G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398219 | |||||||
chr1:218398249 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.347-6920G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398249 | |||||||
chr1:218398415 | A | T | 80 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0092 others(77): Show |
82 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.347-6754A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398415 | |||||||
chr1:218398572 | T | A | 1 | a0001c0001t0078g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.347-6597T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398572 | |||||||
chr1:218398662 | G | A | 80 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0092 others(77): Show |
82 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.347-6507G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398662 | |||||||
chr1:218398680 | C | T | 3 | a0001c0001t0049g0205 a0001c0001t0056g0141 a0001c0001t0061g0086 |
3 | HG02055.hp2 HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.347-6489C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398680 | |||||||
chr1:218398683 | G | A | 1 | a0001c0001t0009g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.347-6486G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398683 | |||||||
chr1:218398733 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-6436G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398733 | |||||||
chr1:218398760 | G | T | 10 | a0001c0001t0002g0091 a0001c0001t0002g0173 a0001c0001t0004g0030 others(7): Show |
10 | HG02074.hp1 NA18943.hp1 NA18986.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-6409G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398760 | |||||||
chr1:218398776 | C | T | 1 | a0001c0001t0017g0146 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.347-6393C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398776 | |||||||
chr1:218398895 | T | G | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-6274T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398895 | |||||||
chr1:218398925 | C | G | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-6244C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218398925 | |||||||
chr1:218399009 | A | G | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-6160A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399009 | |||||||
chr1:218399044 | C | T | 1 | a0001c0001t0038g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.347-6125C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399044 | |||||||
chr1:218399131 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.347-6038C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399131 | |||||||
chr1:218399238 | C | G | 26 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0102 others(23): Show |
26 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.347-5931C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399238 | |||||||
chr1:218399257 | C | T | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-5912C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399257 | |||||||
chr1:218399288 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.347-5881G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399288 | |||||||
chr1:218399353 | G | A | 19 | a0001c0001t0001g0087 a0001c0001t0003g0255 a0001c0001t0004g0223 others(16): Show |
19 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.347-5816G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399353 | |||||||
chr1:218399426 | T | G | 64 | a0001c0001t0001g0087 a0001c0001t0003g0253 a0001c0001t0003g0255 others(61): Show |
64 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.347-5743T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399426 | |||||||
chr1:218399466 | A | G | 67 | a0001c0001t0001g0087 a0001c0001t0003g0227 a0001c0001t0003g0253 others(64): Show |
67 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.347-5703A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399466 | |||||||
chr1:218399708 | A | G | 1 | a0001c0001t0003g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-5461A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399708 | |||||||
chr1:218399764 | T | G | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-5405T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399764 | |||||||
chr1:218399907 | G | A | 12 | a0001c0001t0001g0087 a0001c0001t0004g0223 a0001c0001t0004g0224 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-5262G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218399907 | |||||||
chr1:218400323 | G | A | 3 | a0001c0001t0011g0226 a0001c0001t0020g0004 a0001c0001t0065g0120 |
4 | HG01433.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-4846G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400323 | |||||||
chr1:218400358 | C | G | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-4811C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400358 | |||||||
chr1:218400399 | T | C | 175 | a0001c0001t0001g0061 a0001c0001t0001g0077 a0001c0001t0001g0087 others(172): Show |
177 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.347-4770T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400399 | |||||||
chr1:218400426 | C | A | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-4743C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400426 | |||||||
chr1:218400800 | CCTGACCC others(3): Show |
C | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-4365_347-4356d others(12): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218400800 | ||||||
chr1:218400816 | A | G | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-4353A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400816 | |||||||
chr1:218400824 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.347-4345G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400824 | |||||||
chr1:218400870 | T | C | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.347-4299T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218400870 | |||||||
chr1:218401090 | C | T | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-4079C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401090 | |||||||
chr1:218401100 | G | C | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-4069G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401100 | |||||||
chr1:218401133 | G | A | 1 | a0001c0001t0003g0028 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.347-4036G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401133 | |||||||
chr1:218401228 | A | G | 1 | a0001c0001t0061g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.347-3941A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401228 | |||||||
chr1:218401242 | A | AT | 42 | a0001c0001t0003g0253 a0001c0001t0004g0209 a0001c0001t0006g0088 others(39): Show |
42 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.347-3926dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218401242 | ||||||
chr1:218401447 | C | T | 72 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(69): Show |
72 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.347-3722C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401447 | |||||||
chr1:218401465 | G | A | 5 | a0001c0001t0007g0111 a0001c0001t0014g0174 a0001c0001t0014g0191 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-3704G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401465 | |||||||
chr1:218401530 | G | A | 1 | a0001c0001t0051g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.347-3639G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401530 | |||||||
chr1:218401576 | G | A | 10 | a0001c0001t0002g0091 a0001c0001t0002g0173 a0001c0001t0004g0030 others(7): Show |
10 | HG02074.hp1 NA18943.hp1 NA18986.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-3593G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401576 | |||||||
chr1:218401685 | C | T | 12 | a0001c0001t0001g0087 a0001c0001t0004g0223 a0001c0001t0004g0224 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-3484C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401685 | |||||||
chr1:218401828 | G | A | 5 | a0001c0001t0001g0077 a0001c0001t0003g0218 a0001c0001t0003g0219 others(2): Show |
5 | HG01169.hp1 HG02486.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-3341G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401828 | |||||||
chr1:218401829 | C | T | 1 | a0001c0001t0009g0250 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.347-3340C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401829 | |||||||
chr1:218401834 | C | T | 4 | a0001c0001t0002g0094 a0001c0001t0002g0115 a0001c0001t0004g0003 others(1): Show |
5 | HG00639.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-3335C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401834 | |||||||
chr1:218401860 | G | A | 93 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(90): Show |
95 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.347-3309G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401860 | |||||||
chr1:218401996 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.347-3173G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401996 | |||||||
chr1:218401998 | G | A | 12 | a0001c0001t0001g0087 a0001c0001t0004g0223 a0001c0001t0004g0224 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-3171G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218401998 | |||||||
chr1:218402051 | G | A | 1 | a0001c0001t0049g0205 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.347-3118G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402051 | |||||||
chr1:218402130 | A | G | 226 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(223): Show |
228 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.347-3039A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402130 | |||||||
chr1:218402285 | A | T | 1 | a0001c0001t0010g0020 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.347-2884A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402285 | |||||||
chr1:218402380 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.347-2789A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402380 | |||||||
chr1:218402544 | GA | G | 10 | a0001c0001t0001g0085 a0001c0001t0021g0221 a0001c0001t0021g0228 others(7): Show |
10 | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-2618delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218402544 | ||||||
chr1:218402545 | A | G | 103 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0002g0056 others(100): Show |
104 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.347-2624A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402545 | |||||||
chr1:218402683 | T | C | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-2486T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402683 | |||||||
chr1:218402853 | C | G | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.347-2316C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402853 | |||||||
chr1:218402862 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0027g0270 a0001c0001t0031g0284 |
3 | HG02717.hp2 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.347-2307G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402862 | |||||||
chr1:218402935 | C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.347-2234C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402935 | |||||||
chr1:218402987 | C | T | 1 | a0001c0001t0004g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.347-2182C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218402987 | |||||||
chr1:218403203 | T | G | 2 | a0001c0001t0001g0140 a0001c0001t0050g0168 |
2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.347-1966T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403203 | |||||||
chr1:218403207 | GT | G | 57 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0004g0209 others(54): Show |
57 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(54): Show |
intron_variant | MODIFIER | c.347-1955delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218403207 | ||||||
chr1:218403328 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0082g0286 |
2 | HG01071.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.347-1841G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403328 | |||||||
chr1:218403782 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0003g0256 |
3 | HG02109.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.347-1387G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403782 | |||||||
chr1:218403836 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.347-1333G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403836 | |||||||
chr1:218403953 | G | C | 50 | a0001c0001t0003g0253 a0001c0001t0004g0209 a0001c0001t0006g0088 others(47): Show |
50 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.347-1216G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403953 | |||||||
chr1:218403984 | G | A | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-1185G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218403984 | |||||||
chr1:218404051 | C | CA | 45 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0004g0209 others(42): Show |
45 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.347-1098dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218404051 | ||||||
chr1:218404051 | C | CAA | 9 | a0001c0001t0007g0111 a0001c0001t0007g0203 a0001c0001t0009g0038 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.347-1099_347-1098d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218404051 | ||||||
chr1:218404051 | CA | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0068 others(203): Show |
208 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.347-1098delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218404051 | ||||||
chr1:218404051 | CAA | C | 7 | a0001c0001t0001g0076 a0001c0001t0011g0226 a0001c0001t0011g0260 others(4): Show |
8 | HG01433.hp2 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-1099_347-1098d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 218404051 | ||||||
chr1:218404101 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.347-1068C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218404101 | |||||||
chr1:218404236 | C | T | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.347-933C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 1/6 | chr1 | 218404236 | |||||||
chr1:218405343 | T | TTTGTTG | 38 | a0001c0001t0006g0088 a0001c0001t0006g0119 a0001c0001t0006g0123 others(35): Show |
38 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.510+38_510+43dupGT others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405343 | ||||||
chr1:218405343 | T | TTTGTTGT others(2): Show |
6 | a0001c0001t0003g0253 a0001c0001t0007g0160 a0001c0001t0019g0283 others(3): Show |
6 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+35_510+43dupGT others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405343 | ||||||
chr1:218405343 | T | TTTGTTGT others(5): Show |
2 | a0001c0001t0004g0209 a0001c0001t0018g0277 |
2 | HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.510+32_510+43dupGT others(10): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405343 | ||||||
chr1:218405343 | TTTG | T | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+41_510+43delGT others(1): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405343 | ||||||
chr1:218405384 | A | ACT | 3 | a0001c0001t0003g0022 a0001c0001t0027g0270 a0001c0001t0031g0284 |
3 | HG02717.hp2 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.510+69_510+70dupCT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218405384 | ||||||
chr1:218405422 | T | G | 1 | a0001c0001t0002g0126 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.510+90T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218405422 | |||||||
chr1:218405872 | G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.510+540G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218405872 | |||||||
chr1:218406167 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.510+835C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406167 | |||||||
chr1:218406178 | G | A | 10 | a0001c0001t0007g0111 a0001c0001t0014g0174 a0001c0001t0014g0191 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.510+846G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406178 | |||||||
chr1:218406192 | T | TAC | 110 | a0001c0001t0001g0061 a0001c0001t0001g0077 a0001c0001t0001g0087 others(107): Show |
111 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.510+883_510+884dup others(2): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406192 | ||||||
chr1:218406192 | T | TACAC | 49 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0004g0236 others(46): Show |
49 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(46): Show |
intron_variant | MODIFIER | c.510+881_510+884dup others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406192 | ||||||
chr1:218406192 | T | TACACAC | 3 | a0001c0001t0004g0209 a0001c0001t0026g0278 a0001c0001t0052g0058 |
3 | HG02486.hp1 HG02922.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.510+879_510+884dup others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406192 | ||||||
chr1:218406192 | TAC | T | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+883_510+884del others(2): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406192 | ||||||
chr1:218406212 | C | G | 1 | a0001c0001t0029g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.510+880C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406212 | |||||||
chr1:218406302 | G | A | 57 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0004g0209 others(54): Show |
57 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(54): Show |
intron_variant | MODIFIER | c.510+970G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406302 | |||||||
chr1:218406338 | A | AT | 57 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0004g0209 others(54): Show |
57 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(54): Show |
intron_variant | MODIFIER | c.510+1010dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218406338 | ||||||
chr1:218406409 | G | A | 52 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0004g0209 others(49): Show |
52 | HG01261.hp1 HG01261.hp2 HG01346.hp1 others(49): Show |
intron_variant | MODIFIER | c.510+1077G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406409 | |||||||
chr1:218406511 | A | G | 44 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(41): Show |
44 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.510+1179A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406511 | |||||||
chr1:218406526 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.510+1194C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406526 | |||||||
chr1:218406643 | A | G | 162 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0001g0194 others(159): Show |
163 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(160): Show |
intron_variant | MODIFIER | c.510+1311A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406643 | |||||||
chr1:218406658 | G | T | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+1326G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406658 | |||||||
chr1:218406823 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.510+1491G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406823 | |||||||
chr1:218406850 | C | A | 1 | a0001c0001t0003g0242 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.510+1518C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406850 | |||||||
chr1:218406883 | G | A | 4 | a0001c0001t0006g0119 a0001c0001t0006g0123 a0001c0001t0006g0130 others(1): Show |
4 | HG01496.hp2 HG01928.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1551G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218406883 | |||||||
chr1:218407028 | A | G | 217 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(214): Show |
218 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(215): Show |
intron_variant | MODIFIER | c.510+1696A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407028 | |||||||
chr1:218407117 | A | T | 46 | a0001c0001t0003g0255 a0001c0001t0006g0088 a0001c0001t0006g0101 others(43): Show |
46 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.510+1785A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407117 | |||||||
chr1:218407141 | A | C | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.510+1809A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407141 | |||||||
chr1:218407159 | G | T | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.510+1827G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407159 | |||||||
chr1:218407174 | T | C | 3 | a0001c0001t0001g0108 a0001c0001t0003g0240 a0001c0001t0047g0241 |
3 | HG00741.hp2 HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.510+1842T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407174 | |||||||
chr1:218407426 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+2094C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407426 | |||||||
chr1:218407467 | C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.510+2135C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407467 | |||||||
chr1:218407709 | G | A | 4 | a0001c0001t0001g0103 a0001c0001t0034g0254 a0001c0001t0074g0281 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+2377G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407709 | |||||||
chr1:218407755 | A | G | 6 | a0001c0001t0007g0111 a0001c0001t0007g0160 a0001c0001t0014g0174 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+2423A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407755 | |||||||
chr1:218407760 | G | T | 47 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(44): Show |
47 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.510+2428G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218407760 | |||||||
chr1:218408088 | A | T | 7 | a0001c0001t0003g0253 a0001c0001t0018g0277 a0001c0001t0034g0254 others(4): Show |
7 | HG01884.hp2 HG02717.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+2756A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408088 | |||||||
chr1:218408105 | T | G | 52 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(49): Show |
52 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.510+2773T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408105 | |||||||
chr1:218408167 | T | C | 166 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(163): Show |
167 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.510+2835T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408167 | |||||||
chr1:218408180 | C | T | 6 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(3): Show |
6 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+2848C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408180 | |||||||
chr1:218408221 | G | A | 1 | a0001c0001t0006g0185 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.510+2889G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408221 | |||||||
chr1:218408253 | A | G | 39 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(36): Show |
39 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.510+2921A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408253 | |||||||
chr1:218408275 | T | C | 91 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(88): Show |
91 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.510+2943T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408275 | |||||||
chr1:218408349 | C | T | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.510+3017C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408349 | |||||||
chr1:218408516 | A | G | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+3184A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218408516 | |||||||
chr1:218409021 | C | T | 5 | a0001c0001t0002g0156 a0001c0001t0002g0198 a0001c0001t0004g0026 others(2): Show |
5 | NA18940.hp2 NA18993.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+3689C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409021 | |||||||
chr1:218409089 | G | A | 3 | a0001c0001t0034g0254 a0001c0001t0074g0281 a0001c0001t0085g0213 |
3 | HG02717.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.510+3757G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409089 | |||||||
chr1:218409202 | C | T | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.510+3870C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409202 | |||||||
chr1:218409273 | C | A | 1 | a0001c0001t0062g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510+3941C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409273 | |||||||
chr1:218409294 | A | G | 1 | a0001c0001t0011g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510+3962A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409294 | |||||||
chr1:218409301 | A | G | 1 | a0001c0001t0004g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.510+3969A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409301 | |||||||
chr1:218409436 | T | C | 99 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0002g0056 others(96): Show |
100 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.510+4104T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409436 | |||||||
chr1:218409447 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0003g0049 |
2 | NA19074.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.510+4115G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409447 | |||||||
chr1:218409499 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.510+4167T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409499 | |||||||
chr1:218409598 | A | G | 5 | a0001c0001t0002g0204 a0001c0001t0013g0211 a0001c0001t0013g0212 others(2): Show |
5 | HG02622.hp1 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+4266A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409598 | |||||||
chr1:218409618 | T | C | 1 | a0001c0001t0052g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.510+4286T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409618 | |||||||
chr1:218409665 | GA | G | 54 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(51): Show |
54 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.510+4343delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218409665 | ||||||
chr1:218409675 | A | C | 11 | a0001c0001t0007g0111 a0001c0001t0007g0160 a0001c0001t0014g0174 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+4343A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409675 | |||||||
chr1:218409889 | A | G | 3 | a0001c0001t0004g0209 a0001c0001t0019g0283 a0001c0001t0027g0269 |
3 | HG02559.hp2 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.510+4557A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218409889 | |||||||
chr1:218410075 | C | T | 2 | a0001c0001t0003g0253 a0001c0001t0018g0277 |
2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.510+4743C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410075 | |||||||
chr1:218410156 | C | A | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.510+4824C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410156 | |||||||
chr1:218410428 | C | G | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+5096C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410428 | |||||||
chr1:218410485 | C | T | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+5153C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410485 | |||||||
chr1:218410958 | A | G | 6 | a0001c0001t0002g0173 a0001c0001t0010g0020 a0001c0001t0030g0009 others(3): Show |
6 | NA18986.hp2 NA18991.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+5626A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410958 | |||||||
chr1:218410972 | G | T | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+5640G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410972 | |||||||
chr1:218410979 | T | C | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+5647T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218410979 | |||||||
chr1:218411033 | A | ATCC | 29 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0096 others(26): Show |
29 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.510+5703_510+5705d others(5): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411033 | ||||||
chr1:218411075 | A | G | 1 | a0001c0001t0016g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.510+5743A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411075 | |||||||
chr1:218411077 | C | T | 54 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(51): Show |
54 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.510+5745C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411077 | |||||||
chr1:218411125 | C | T | 1 | a0001c0001t0034g0254 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.510+5793C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411125 | |||||||
chr1:218411155 | T | G | 6 | a0001c0001t0001g0103 a0001c0001t0003g0255 a0001c0001t0004g0209 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+5823T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411155 | |||||||
chr1:218411250 | A | C | 1 | a0001c0001t0040g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.510+5918A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411250 | |||||||
chr1:218411381 | T | C | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+6049T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411381 | |||||||
chr1:218411610 | A | C | 117 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(114): Show |
117 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(114): Show |
intron_variant | MODIFIER | c.510+6278A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411610 | |||||||
chr1:218411640 | C | T | 1 | a0001c0001t0004g0040 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.510+6308C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411640 | |||||||
chr1:218411789 | C | T | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+6457C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411789 | |||||||
chr1:218411812 | C | CAGAG | 43 | a0001c0001t0001g0103 a0001c0001t0004g0209 a0001c0001t0006g0088 others(40): Show |
43 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(40): Show |
intron_variant | MODIFIER | c.510+6482_510+6485d others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411812 | ||||||
chr1:218411812 | C | T | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+6480C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411812 | |||||||
chr1:218411845 | A | T | 2 | a0001c0001t0018g0282 a0001c0001t0029g0267 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.510+6513A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411845 | |||||||
chr1:218411864 | C | CA | 43 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0175 others(40): Show |
43 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(40): Show |
intron_variant | MODIFIER | c.510+6550dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411864 | ||||||
chr1:218411864 | C | CAA | 8 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0035g0220 others(5): Show |
8 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+6549_510+6550d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411864 | ||||||
chr1:218411864 | CA | C | 29 | a0001c0001t0001g0061 a0001c0001t0001g0085 a0001c0001t0001g0158 others(26): Show |
30 | HG01109.hp1 HG01433.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.510+6550delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218411864 | ||||||
chr1:218411886 | C | T | 1 | a0001c0001t0010g0018 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.510+6554C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411886 | |||||||
chr1:218411906 | C | T | 39 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(36): Show |
39 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.510+6574C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218411906 | |||||||
chr1:218412071 | C | T | 1 | a0001c0001t0007g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.510+6739C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412071 | |||||||
chr1:218412479 | C | T | 92 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(89): Show |
92 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.510+7147C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412479 | |||||||
chr1:218412527 | G | A | 5 | a0001c0001t0007g0111 a0001c0001t0014g0174 a0001c0001t0014g0191 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+7195G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412527 | |||||||
chr1:218412573 | C | G | 9 | a0001c0001t0003g0022 a0001c0001t0011g0226 a0001c0001t0011g0260 others(6): Show |
10 | HG01433.hp2 HG01891.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.510+7241C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412573 | |||||||
chr1:218412599 | C | T | 1 | a0001c0001t0004g0040 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.510+7267C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412599 | |||||||
chr1:218412613 | C | A | 1 | a0001c0001t0074g0281 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510+7281C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412613 | |||||||
chr1:218412790 | A | G | 225 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(222): Show |
227 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(224): Show |
intron_variant | MODIFIER | c.510+7458A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412790 | |||||||
chr1:218412872 | A | T | 93 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(90): Show |
93 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.510+7540A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412872 | |||||||
chr1:218412886 | G | A | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+7554G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412886 | |||||||
chr1:218412955 | T | C | 4 | a0001c0001t0001g0103 a0001c0001t0004g0209 a0001c0001t0019g0283 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+7623T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412955 | |||||||
chr1:218412956 | T | C | 1 | a0001c0001t0065g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.510+7624T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412956 | |||||||
chr1:218412971 | T | C | 4 | a0001c0001t0001g0103 a0001c0001t0004g0209 a0001c0001t0019g0283 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+7639T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412971 | |||||||
chr1:218412991 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.510+7659T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218412991 | |||||||
chr1:218413180 | T | C | 39 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(36): Show |
39 | HG01258.hp1 HG01261.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.510+7848T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413180 | |||||||
chr1:218413363 | G | A | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+8031G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413363 | |||||||
chr1:218413515 | T | C | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+8183T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413515 | |||||||
chr1:218413552 | C | T | 1 | a0001c0001t0072g0064 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.510+8220C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413552 | |||||||
chr1:218413769 | C | T | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+8437C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413769 | |||||||
chr1:218413824 | T | C | 7 | a0001c0001t0001g0103 a0001c0001t0004g0209 a0001c0001t0019g0283 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+8492T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413824 | |||||||
chr1:218413940 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.510+8608G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218413940 | |||||||
chr1:218414024 | G | C | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+8692G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414024 | |||||||
chr1:218414145 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.510+8813G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414145 | |||||||
chr1:218414195 | A | T | 3 | a0001c0001t0049g0205 a0001c0001t0056g0141 a0001c0001t0061g0086 |
3 | HG02055.hp2 HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.510+8863A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414195 | |||||||
chr1:218414226 | T | TGC | 3 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0003g0256 |
3 | HG02109.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.510+8895_510+8896d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218414226 | ||||||
chr1:218414227 | G | GCA | 34 | a0001c0001t0001g0001 a0001c0001t0001g0083 a0001c0001t0001g0093 others(31): Show |
35 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.510+8921_510+8922d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218414227 | ||||||
chr1:218414227 | G | GCACACA | 3 | a0001c0001t0001g0114 a0001c0001t0004g0209 a0001c0001t0027g0269 |
3 | HG02615.hp2 HG02922.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.510+8917_510+8922d others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218414227 | ||||||
chr1:218414227 | GCA | G | 129 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(126): Show |
131 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.510+8921_510+8922d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218414227 | ||||||
chr1:218414229 | A | G | 46 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(43): Show |
46 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.510+8897A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414229 | |||||||
chr1:218414231 | A | G | 29 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0096 others(26): Show |
29 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.510+8899A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414231 | |||||||
chr1:218414254 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510+8922C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414254 | |||||||
chr1:218414294 | A | G | 225 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(222): Show |
227 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(224): Show |
intron_variant | MODIFIER | c.510+8962A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414294 | |||||||
chr1:218414685 | A | C | 9 | a0001c0001t0001g0103 a0001c0001t0003g0255 a0001c0001t0004g0209 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.510+9353A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414685 | |||||||
chr1:218414796 | CATGCAG | C | 92 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(89): Show |
92 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.510+9465_510+9470d others(8): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414796 | |||||||
chr1:218414937 | G | A | 108 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0002g0056 others(105): Show |
110 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.510+9605G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218414937 | |||||||
chr1:218415626 | C | G | 7 | a0001c0001t0003g0253 a0001c0001t0011g0208 a0001c0001t0018g0277 others(4): Show |
7 | HG01884.hp2 HG03471.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+10294C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415626 | |||||||
chr1:218415673 | C | T | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+10341C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415673 | |||||||
chr1:218415694 | C | CA | 61 | a0001c0001t0001g0117 a0001c0001t0001g0159 a0001c0001t0002g0057 others(58): Show |
62 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.510+10366dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218415694 | ||||||
chr1:218415694 | C | CAA | 40 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0002g0056 others(37): Show |
40 | HG00621.hp1 HG01071.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.510+10365_510+1036 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218415694 | ||||||
chr1:218415694 | C | CAAA | 7 | a0001c0001t0001g0087 a0001c0001t0002g0129 a0001c0001t0002g0131 others(4): Show |
7 | HG02055.hp2 HG02572.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+10364_510+1036 others(7): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218415694 | ||||||
chr1:218415697 | AAG | A | 41 | a0001c0001t0001g0096 a0001c0001t0006g0088 a0001c0001t0006g0101 others(38): Show |
41 | HG00738.hp1 HG01243.hp1 HG01258.hp1 others(38): Show |
intron_variant | MODIFIER | c.510+10367_510+1036 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218415697 | ||||||
chr1:218415698 | AG | A | 39 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(36): Show |
39 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.510+10367delG | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415698 | |||||||
chr1:218415699 | G | A | 145 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0001g0102 others(142): Show |
147 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.510+10367G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415699 | |||||||
chr1:218415722 | A | G | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+10390A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415722 | |||||||
chr1:218415776 | C | G | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.510+10444C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415776 | |||||||
chr1:218415855 | T | C | 225 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(222): Show |
227 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(224): Show |
intron_variant | MODIFIER | c.510+10523T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415855 | |||||||
chr1:218415860 | A | G | 3 | a0001c0001t0002g0173 a0001c0001t0010g0020 a0001c0001t0033g0044 |
3 | NA18986.hp2 NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.510+10528A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218415860 | |||||||
chr1:218416103 | T | C | 7 | a0001c0001t0001g0103 a0001c0001t0004g0209 a0001c0001t0019g0283 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+10771T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416103 | |||||||
chr1:218416124 | TG | T | 42 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(39): Show |
42 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.510+10797delG | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218416124 | ||||||
chr1:218416178 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0002g0129 |
2 | NA18995.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.510+10846C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416178 | |||||||
chr1:218416292 | C | CT | 10 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(7): Show |
10 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.510+10970dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218416292 | ||||||
chr1:218416296 | T | C | 1 | a0001c0001t0065g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.510+10964T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416296 | |||||||
chr1:218416375 | G | T | 3 | a0001c0001t0004g0209 a0001c0001t0019g0283 a0001c0001t0027g0269 |
3 | HG02559.hp2 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.510+11043G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416375 | |||||||
chr1:218416605 | C | T | 2 | a0001c0001t0021g0221 a0001c0001t0021g0228 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.510+11273C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416605 | |||||||
chr1:218416649 | C | T | 2 | a0001c0001t0021g0221 a0001c0001t0021g0228 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.510+11317C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416649 | |||||||
chr1:218416706 | C | G | 1 | a0003c0004t0003g0042 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.510+11374C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416706 | |||||||
chr1:218416813 | A | G | 52 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0081 others(49): Show |
52 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.510+11481A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416813 | |||||||
chr1:218416884 | A | G | 10 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0003g0218 others(7): Show |
10 | HG01169.hp1 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.510+11552A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218416884 | |||||||
chr1:218417156 | A | C | 7 | a0001c0001t0007g0111 a0001c0001t0007g0160 a0001c0001t0014g0174 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+11824A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417156 | |||||||
chr1:218417298 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.510+11966C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417298 | |||||||
chr1:218417303 | G | A | 1 | a0001c0001t0020g0004 | 2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.510+11971G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417303 | |||||||
chr1:218417313 | G | A | 27 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0096 others(24): Show |
27 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.510+11981G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417313 | |||||||
chr1:218417372 | T | G | 4 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0003g0256 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+12040T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417372 | |||||||
chr1:218417430 | A | G | 3 | a0001c0001t0011g0225 a0001c0001t0028g0275 a0001c0001t0028g0276 |
3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.510+12098A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417430 | |||||||
chr1:218417531 | G | T | 1 | a0001c0001t0063g0187 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.510+12199G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417531 | |||||||
chr1:218417705 | T | C | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+12373T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417705 | |||||||
chr1:218417805 | G | A | 1 | a0001c0001t0068g0132 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.510+12473G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417805 | |||||||
chr1:218417852 | T | G | 5 | a0001c0001t0002g0112 a0001c0001t0002g0195 a0001c0001t0004g0233 others(2): Show |
5 | HG01978.hp1 HG02056.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+12520T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417852 | |||||||
chr1:218417977 | G | A | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.510+12645G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218417977 | |||||||
chr1:218418200 | T | C | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.510+12868T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418200 | |||||||
chr1:218418281 | G | A | 166 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(163): Show |
169 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(166): Show |
intron_variant | MODIFIER | c.510+12949G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418281 | |||||||
chr1:218418349 | G | A | 1 | a0001c0001t0006g0176 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.510+13017G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418349 | |||||||
chr1:218418423 | G | A | 1 | a0001c0001t0011g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.510+13091G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418423 | |||||||
chr1:218418640 | G | T | 5 | a0001c0001t0002g0156 a0001c0001t0002g0198 a0001c0001t0004g0026 others(2): Show |
5 | NA18940.hp2 NA18993.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+13308G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418640 | |||||||
chr1:218418704 | G | C | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+13372G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418704 | |||||||
chr1:218418773 | G | A | 54 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(51): Show |
55 | HG01109.hp2 HG01243.hp1 HG01258.hp1 others(52): Show |
intron_variant | MODIFIER | c.510+13441G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418773 | |||||||
chr1:218418818 | G | T | 2 | a0001c0001t0037g0229 a0001c0001t0052g0058 |
2 | HG03669.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.510+13486G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418818 | |||||||
chr1:218418920 | C | T | 1 | a0001c0001t0038g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.510+13588C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418920 | |||||||
chr1:218418932 | T | C | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+13600T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218418932 | |||||||
chr1:218419192 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.510+13860T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419192 | |||||||
chr1:218419389 | G | A | 1 | a0001c0001t0018g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.510+14057G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419389 | |||||||
chr1:218419528 | T | C | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.510+14196T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419528 | |||||||
chr1:218419563 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.510+14231G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419563 | |||||||
chr1:218419645 | A | C | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+14313A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419645 | |||||||
chr1:218419695 | C | T | 101 | a0001c0001t0001g0151 a0001c0001t0002g0056 a0001c0001t0002g0057 others(98): Show |
103 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.510+14363C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218419695 | |||||||
chr1:218420080 | G | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-14002G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218420080 | |||||||
chr1:218420478 | A | T | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-13604A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218420478 | |||||||
chr1:218420740 | G | T | 3 | a0001c0001t0002g0173 a0001c0001t0010g0020 a0001c0001t0033g0044 |
3 | NA18986.hp2 NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.511-13342G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218420740 | |||||||
chr1:218420887 | GC | G | 3 | a0001c0001t0011g0225 a0001c0001t0028g0275 a0001c0001t0028g0276 |
3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.511-13194delC | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218420887 | |||||||
chr1:218421142 | G | A | 2 | a0001c0001t0002g0118 a0001c0001t0002g0167 |
2 | HG01346.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.511-12940G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421142 | |||||||
chr1:218421246 | T | C | 5 | a0001c0001t0011g0208 a0001c0001t0037g0229 a0001c0001t0050g0168 others(2): Show |
5 | HG03471.hp1 HG03669.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-12836T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421246 | |||||||
chr1:218421373 | G | GT | 49 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0085 others(46): Show |
49 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.511-12694dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218421373 | ||||||
chr1:218421373 | GT | G | 158 | a0001c0001t0001g0151 a0001c0001t0002g0056 a0001c0001t0002g0057 others(155): Show |
161 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.511-12694delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218421373 | ||||||
chr1:218421376 | T | G | 1 | a0001c0001t0004g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.511-12706T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421376 | |||||||
chr1:218421377 | T | G | 100 | a0001c0001t0001g0151 a0001c0001t0002g0056 a0001c0001t0002g0057 others(97): Show |
102 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.511-12705T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421377 | |||||||
chr1:218421406 | A | AT | 51 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(48): Show |
52 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.511-12674dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218421406 | ||||||
chr1:218421413 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.511-12669A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421413 | |||||||
chr1:218421578 | G | T | 168 | a0001c0001t0001g0151 a0001c0001t0002g0056 a0001c0001t0002g0057 others(165): Show |
171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.511-12504G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421578 | |||||||
chr1:218421613 | A | C | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-12469A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421613 | |||||||
chr1:218421653 | TA | T | 10 | a0001c0001t0011g0208 a0001c0001t0021g0221 a0001c0001t0021g0228 others(7): Show |
10 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-12421delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218421653 | ||||||
chr1:218421772 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.511-12310C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421772 | |||||||
chr1:218421984 | G | A | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-12098G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218421984 | |||||||
chr1:218422019 | G | C | 1 | a0001c0001t0030g0009 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.511-12063G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422019 | |||||||
chr1:218422244 | G | A | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-11838G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422244 | |||||||
chr1:218422257 | A | G | 1 | a0001c0001t0007g0113 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.511-11825A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422257 | |||||||
chr1:218422318 | A | G | 1 | a0001c0001t0060g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.511-11764A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422318 | |||||||
chr1:218422373 | A | G | 1 | a0001c0001t0018g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.511-11709A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422373 | |||||||
chr1:218422378 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.511-11704C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422378 | |||||||
chr1:218422458 | C | T | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-11624C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422458 | |||||||
chr1:218422565 | T | C | 1 | a0001c0001t0008g0182 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.511-11517T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422565 | |||||||
chr1:218422590 | G | A | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-11492G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422590 | |||||||
chr1:218422769 | C | T | 1 | a0001c0001t0006g0119 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.511-11313C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422769 | |||||||
chr1:218422872 | A | G | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.511-11210A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218422872 | |||||||
chr1:218423119 | A | G | 168 | a0001c0001t0001g0151 a0001c0001t0002g0056 a0001c0001t0002g0057 others(165): Show |
171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.511-10963A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423119 | |||||||
chr1:218423299 | G | T | 168 | a0001c0001t0001g0151 a0001c0001t0002g0056 a0001c0001t0002g0057 others(165): Show |
171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.511-10783G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423299 | |||||||
chr1:218423411 | T | C | 1 | a0001c0001t0003g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.511-10671T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423411 | |||||||
chr1:218423415 | G | A | 1 | a0001c0001t0009g0033 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.511-10667G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423415 | |||||||
chr1:218423657 | C | T | 1 | a0001c0001t0047g0241 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.511-10425C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423657 | |||||||
chr1:218423658 | G | A | 2 | a0001c0001t0074g0281 a0001c0001t0085g0213 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.511-10424G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423658 | |||||||
chr1:218423702 | G | A | 171 | a0001c0001t0001g0103 a0001c0001t0001g0151 a0001c0001t0002g0056 others(168): Show |
174 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(171): Show |
intron_variant | MODIFIER | c.511-10380G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423702 | |||||||
chr1:218423955 | C | G | 168 | a0001c0001t0001g0151 a0001c0001t0002g0056 a0001c0001t0002g0057 others(165): Show |
171 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.511-10127C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423955 | |||||||
chr1:218423963 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.511-10119C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423963 | |||||||
chr1:218423964 | G | A | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-10118G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218423964 | |||||||
chr1:218424075 | C | T | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-10007C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424075 | |||||||
chr1:218424290 | G | A | 91 | a0001c0001t0001g0151 a0001c0001t0002g0056 a0001c0001t0002g0057 others(88): Show |
93 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.511-9792G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424290 | |||||||
chr1:218424517 | C | T | 101 | a0001c0001t0001g0151 a0001c0001t0002g0056 a0001c0001t0002g0057 others(98): Show |
103 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-9565C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424517 | |||||||
chr1:218424747 | G | T | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-9335G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424747 | |||||||
chr1:218424971 | G | T | 1 | a0001c0001t0005g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.511-9111G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424971 | |||||||
chr1:218424986 | C | G | 155 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(152): Show |
158 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(155): Show |
intron_variant | MODIFIER | c.511-9096C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218424986 | |||||||
chr1:218425042 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0152 |
3 | NA18974.hp1 NA19080.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.511-9040A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425042 | |||||||
chr1:218425068 | G | T | 156 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(153): Show |
159 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.511-9014G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425068 | |||||||
chr1:218425127 | A | T | 156 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(153): Show |
159 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.511-8955A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425127 | |||||||
chr1:218425142 | C | T | 166 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(163): Show |
169 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(166): Show |
intron_variant | MODIFIER | c.511-8940C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425142 | |||||||
chr1:218425235 | T | G | 2 | a0001c0001t0001g0114 a0001c0001t0038g0041 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.511-8847T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425235 | |||||||
chr1:218425276 | C | T | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-8806C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425276 | |||||||
chr1:218425313 | T | C | 1 | a0001c0001t0065g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.511-8769T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425313 | |||||||
chr1:218425332 | C | G | 5 | a0001c0001t0011g0208 a0001c0001t0037g0229 a0001c0001t0050g0168 others(2): Show |
5 | HG03471.hp1 HG03669.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-8750C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425332 | |||||||
chr1:218425364 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.511-8718C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425364 | |||||||
chr1:218425399 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.511-8683G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425399 | |||||||
chr1:218425455 | C | T | 1 | a0001c0001t0012g0014 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.511-8627C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425455 | |||||||
chr1:218425477 | G | A | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-8605G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425477 | |||||||
chr1:218425733 | C | T | 1 | a0001c0001t0013g0245 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.511-8349C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425733 | |||||||
chr1:218425837 | C | A | 1 | a0001c0001t0002g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.511-8245C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425837 | |||||||
chr1:218425850 | A | C | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-8232A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218425850 | |||||||
chr1:218426047 | G | A | 2 | a0001c0001t0050g0168 a0001c0001t0051g0055 |
2 | HG04228.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.511-8035G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426047 | |||||||
chr1:218426252 | C | G | 1 | a0001c0001t0089g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.511-7830C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426252 | |||||||
chr1:218426490 | T | C | 3 | a0001c0001t0053g0186 a0001c0001t0054g0149 a0001c0001t0090g0012 |
3 | NA18967.hp2 NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.511-7592T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426490 | |||||||
chr1:218426577 | T | C | 7 | a0001c0001t0005g0072 a0001c0001t0005g0073 a0001c0001t0005g0074 others(4): Show |
7 | HG02040.hp2 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-7505T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426577 | |||||||
chr1:218426756 | A | G | 1 | a0001c0001t0037g0229 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-7326A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426756 | |||||||
chr1:218426951 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0188 a0001c0001t0003g0237 |
3 | HG00558.hp2 HG02523.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.511-7131C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218426951 | |||||||
chr1:218427059 | C | T | 1 | a0001c0001t0082g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511-7023C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427059 | |||||||
chr1:218427077 | C | T | 157 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(154): Show |
160 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.511-7005C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427077 | |||||||
chr1:218427477 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.511-6605C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427477 | |||||||
chr1:218427523 | C | T | 1 | a0001c0001t0016g0066 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.511-6559C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427523 | |||||||
chr1:218427581 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0009g0222 a0001c0001t0029g0267 others(1): Show |
4 | HG01169.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-6501G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427581 | |||||||
chr1:218427641 | A | G | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.511-6441A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427641 | |||||||
chr1:218427963 | G | A | 52 | a0001c0001t0002g0056 a0001c0001t0002g0071 a0001c0001t0002g0092 others(49): Show |
53 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.511-6119G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218427963 | |||||||
chr1:218428563 | GTT | G | 47 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(44): Show |
47 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.511-5516_511-5515d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218428563 | ||||||
chr1:218428622 | G | C | 1 | a0001c0001t0006g0101 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.511-5460G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218428622 | |||||||
chr1:218428739 | C | G | 4 | a0001c0001t0002g0095 a0001c0001t0002g0138 a0001c0001t0002g0179 others(1): Show |
4 | HG00621.hp1 NA18949.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-5343C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218428739 | |||||||
chr1:218428792 | T | C | 56 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(53): Show |
56 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.511-5290T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218428792 | |||||||
chr1:218428793 | G | A | 1 | a0001c0001t0019g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511-5289G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218428793 | |||||||
chr1:218428972 | C | CT | 95 | a0001c0001t0001g0061 a0001c0001t0001g0097 a0001c0001t0001g0103 others(92): Show |
97 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.511-5086dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218428972 | ||||||
chr1:218428972 | C | CTT | 10 | a0001c0001t0001g0158 a0001c0001t0002g0098 a0001c0001t0002g0179 others(7): Show |
10 | HG01891.hp1 HG02056.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.511-5087_511-5086d others(4): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218428972 | ||||||
chr1:218428972 | CT | C | 33 | a0001c0001t0003g0248 a0001c0001t0006g0088 a0001c0001t0006g0101 others(30): Show |
33 | HG01258.hp1 HG01261.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.511-5086delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218428972 | ||||||
chr1:218429058 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-5024G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429058 | |||||||
chr1:218429105 | C | T | 1 | a0001c0001t0018g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.511-4977C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429105 | |||||||
chr1:218429229 | C | A | 2 | a0001c0001t0009g0033 a0001c0001t0009g0038 |
2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.511-4853C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429229 | |||||||
chr1:218429250 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.511-4832G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429250 | |||||||
chr1:218429379 | A | G | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-4703A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429379 | |||||||
chr1:218429518 | C | G | 3 | a0001c0001t0005g0072 a0001c0001t0005g0073 a0001c0001t0005g0074 |
3 | NA18964.hp1 NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.511-4564C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429518 | |||||||
chr1:218429746 | C | T | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-4336C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429746 | |||||||
chr1:218429918 | T | C | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-4164T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218429918 | |||||||
chr1:218430132 | C | T | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.511-3950C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430132 | |||||||
chr1:218430251 | G | A | 6 | a0001c0001t0003g0022 a0001c0001t0027g0270 a0001c0001t0031g0284 others(3): Show |
6 | HG02717.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-3831G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430251 | |||||||
chr1:218430264 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-3818G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430264 | |||||||
chr1:218430274 | A | T | 1 | a0001c0001t0004g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.511-3808A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430274 | |||||||
chr1:218430401 | A | G | 1 | a0001c0001t0027g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-3681A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430401 | |||||||
chr1:218430500 | G | T | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-3582G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430500 | |||||||
chr1:218430570 | C | G | 1 | a0001c0001t0011g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.511-3512C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430570 | |||||||
chr1:218430654 | G | T | 1 | a0001c0001t0016g0062 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.511-3428G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430654 | |||||||
chr1:218430732 | C | T | 1 | a0001c0001t0079g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.511-3350C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430732 | |||||||
chr1:218430946 | G | A | 7 | a0001c0001t0009g0033 a0001c0001t0009g0038 a0001c0001t0009g0222 others(4): Show |
7 | HG01261.hp2 HG02630.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-3136G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218430946 | |||||||
chr1:218431050 | C | A | 52 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(49): Show |
53 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.511-3032C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431050 | |||||||
chr1:218431124 | A | G | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.511-2958A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431124 | |||||||
chr1:218431273 | A | G | 1 | a0001c0002t0002g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.511-2809A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431273 | |||||||
chr1:218431284 | C | T | 2 | a0001c0001t0002g0071 a0001c0001t0066g0171 |
2 | NA18944.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.511-2798C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431284 | |||||||
chr1:218431336 | G | A | 157 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(154): Show |
160 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.511-2746G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431336 | |||||||
chr1:218431367 | C | T | 90 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(87): Show |
92 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.511-2715C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431367 | |||||||
chr1:218431566 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0029g0266 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.511-2516A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431566 | |||||||
chr1:218431923 | A | G | 1 | a0001c0001t0003g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.511-2159A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431923 | |||||||
chr1:218431963 | T | C | 52 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(49): Show |
53 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.511-2119T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218431963 | |||||||
chr1:218432117 | T | C | 1 | a0001c0001t0003g0242 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.511-1965T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432117 | |||||||
chr1:218432119 | G | A | 157 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(154): Show |
160 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.511-1963G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432119 | |||||||
chr1:218432159 | A | G | 1 | a0001c0001t0037g0229 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-1923A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432159 | |||||||
chr1:218432262 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.511-1820A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432262 | |||||||
chr1:218432267 | G | A | 167 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(164): Show |
170 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.511-1815G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432267 | |||||||
chr1:218432270 | G | A | 2 | a0001c0001t0009g0222 a0001c0001t0089g0011 |
2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.511-1812G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432270 | |||||||
chr1:218432293 | T | C | 101 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(98): Show |
103 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-1789T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432293 | |||||||
chr1:218432379 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.511-1703G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432379 | |||||||
chr1:218432411 | A | C | 1 | a0001c0001t0049g0205 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.511-1671A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432411 | |||||||
chr1:218432437 | C | A | 3 | a0001c0001t0011g0225 a0001c0001t0028g0275 a0001c0001t0028g0276 |
3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.511-1645C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432437 | |||||||
chr1:218432450 | T | C | 1 | a0001c0001t0081g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-1632T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432450 | |||||||
chr1:218432504 | A | G | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-1578A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432504 | |||||||
chr1:218432608 | C | G | 4 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0003g0256 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-1474C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432608 | |||||||
chr1:218432614 | T | C | 95 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(92): Show |
97 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.511-1468T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432614 | |||||||
chr1:218432664 | A | G | 3 | a0001c0001t0011g0225 a0001c0001t0028g0275 a0001c0001t0028g0276 |
3 | HG01109.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.511-1418A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432664 | |||||||
chr1:218432810 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.511-1272C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432810 | |||||||
chr1:218432859 | C | T | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511-1223C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432859 | |||||||
chr1:218432881 | G | A | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.511-1201G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218432881 | |||||||
chr1:218433030 | T | A | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-1052T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433030 | |||||||
chr1:218433072 | A | AT | 5 | a0001c0001t0011g0208 a0001c0001t0011g0226 a0001c0001t0020g0004 others(2): Show |
6 | HG01433.hp2 HG01891.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-1002dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 218433072 | ||||||
chr1:218433126 | T | G | 4 | a0001c0001t0037g0229 a0001c0001t0050g0168 a0001c0001t0051g0055 others(1): Show |
4 | HG03669.hp1 HG04228.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-956T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433126 | |||||||
chr1:218433138 | G | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.511-944G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433138 | |||||||
chr1:218433405 | G | A | 6 | a0001c0001t0007g0160 a0001c0001t0014g0174 a0001c0001t0014g0191 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-677G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433405 | |||||||
chr1:218433533 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-549A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433533 | |||||||
chr1:218433578 | A | C | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.511-504A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433578 | |||||||
chr1:218433606 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0169 |
2 | HG00140.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.511-476G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433606 | |||||||
chr1:218433955 | C | A | 2 | a0001c0001t0007g0078 a0001c0001t0007g0079 |
2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.511-127C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218433955 | |||||||
chr1:218434009 | G | C | 5 | a0001c0001t0002g0204 a0001c0001t0013g0211 a0001c0001t0013g0212 others(2): Show |
5 | HG02622.hp1 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-73G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 2/6 | chr1 | 218434009 | |||||||
chr1:218434221 | A | C | 3 | a0001c0001t0001g0103 a0001c0001t0003g0255 a0001c0001t0083g0262 |
3 | HG02109.hp2 HG02257.hp2 HG02886.hp1 |
splice_region_variant&intron_variant | LOW | c.643+7A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 3/6 | chr1 | 218434221 | |||||||
chr1:218434506 | A | G | 5 | a0001c0001t0002g0204 a0001c0001t0013g0211 a0001c0001t0013g0212 others(2): Show |
5 | HG02622.hp1 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+58A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434506 | |||||||
chr1:218434519 | T | C | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.754+71T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434519 | |||||||
chr1:218434781 | G | T | 5 | a0001c0001t0011g0208 a0001c0001t0011g0226 a0001c0001t0020g0004 others(2): Show |
6 | HG01433.hp2 HG01891.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+333G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434781 | |||||||
chr1:218434782 | A | G | 1 | a0001c0001t0064g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.754+334A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434782 | |||||||
chr1:218434966 | A | G | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.754+518A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218434966 | |||||||
chr1:218435180 | C | T | 1 | a0001c0001t0004g0234 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.754+732C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218435180 | |||||||
chr1:218435215 | A | T | 1 | a0001c0001t0002g0127 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.755-755A>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218435215 | |||||||
chr1:218435300 | G | C | 1 | a0001c0001t0009g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.755-670G>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218435300 | |||||||
chr1:218435764 | C | A | 1 | a0001c0001t0032g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.755-206C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 4/6 | chr1 | 218435764 | |||||||
chr1:218436224 | T | G | 1 | a0001c0001t0003g0256 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.932+77T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436224 | |||||||
chr1:218436259 | T | G | 1 | a0001c0001t0073g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.932+112T>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436259 | |||||||
chr1:218436360 | A | G | 167 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(164): Show |
170 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.932+213A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436360 | |||||||
chr1:218436394 | G | A | 2 | a0001c0001t0043g0238 a0001c0001t0064g0134 |
2 | HG01081.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.932+247G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436394 | |||||||
chr1:218436586 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.932+439C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436586 | |||||||
chr1:218436730 | A | G | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.932+583A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436730 | |||||||
chr1:218436912 | C | T | 167 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(164): Show |
170 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.933-431C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218436912 | |||||||
chr1:218437022 | A | G | 1 | a0001c0001t0018g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.933-321A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218437022 | |||||||
chr1:218437092 | C | A | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-251C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | chr1 | 218437092 | |||||||
chr1:218437320 | C | CT | 6 | a0001c0001t0001g0103 a0001c0001t0003g0255 a0001c0001t0003g0256 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.933-6dupT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 218437320 | ||||||
chr1:218437320 | CT | C | 156 | a0001c0001t0001g0084 a0001c0001t0001g0140 a0001c0001t0002g0056 others(153): Show |
159 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(156): Show |
splice_region_variant&intron_variant | LOW | c.933-6delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 218437320 | ||||||
chr1:218437577 | T | C | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1086+81T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218437577 | |||||||
chr1:218437694 | C | T | 3 | a0001c0001t0049g0205 a0001c0001t0056g0141 a0001c0001t0061g0086 |
3 | HG02055.hp2 HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1086+198C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218437694 | |||||||
chr1:218437839 | C | A | 24 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(21): Show |
24 | HG01258.hp1 HG01496.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.1086+343C>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218437839 | |||||||
chr1:218437879 | G | T | 1 | a0001c0001t0019g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1086+383G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218437879 | |||||||
chr1:218438031 | A | G | 1 | a0001c0001t0007g0110 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1086+535A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438031 | |||||||
chr1:218438061 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1086+565T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438061 | |||||||
chr1:218438133 | C | G | 45 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(42): Show |
45 | HG01243.hp1 HG01258.hp1 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.1086+637C>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438133 | |||||||
chr1:218438281 | G | A | 1 | a0001c0001t0012g0014 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1086+785G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438281 | |||||||
chr1:218438387 | A | G | 6 | a0001c0001t0003g0022 a0001c0001t0027g0270 a0001c0001t0031g0284 others(3): Show |
6 | HG02717.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086+891A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438387 | |||||||
chr1:218438536 | A | G | 234 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0077 others(231): Show |
237 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(234): Show |
intron_variant | MODIFIER | c.1086+1040A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438536 | |||||||
chr1:218438558 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1086+1062G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438558 | |||||||
chr1:218438666 | A | G | 1 | a0001c0001t0019g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1086+1170A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438666 | |||||||
chr1:218438670 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1086+1174C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438670 | |||||||
chr1:218438830 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1086+1334C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438830 | |||||||
chr1:218438875 | G | A | 1 | a0001c0001t0058g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1086+1379G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438875 | |||||||
chr1:218438935 | C | T | 4 | a0001c0001t0037g0229 a0001c0001t0050g0168 a0001c0001t0051g0055 others(1): Show |
4 | HG03669.hp1 HG04228.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086+1439C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218438935 | |||||||
chr1:218439002 | G | A | 5 | a0001c0001t0004g0223 a0001c0001t0004g0224 a0001c0001t0004g0252 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1086+1506G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439002 | |||||||
chr1:218439107 | CA | C | 106 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0081 others(103): Show |
107 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.1086+1631delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218439107 | ||||||
chr1:218439107 | CAA | C | 111 | a0001c0001t0001g0103 a0001c0001t0002g0056 a0001c0001t0002g0057 others(108): Show |
113 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.1086+1630_1086+163 others(6): Show |
TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218439107 | ||||||
chr1:218439165 | C | T | 2 | a0001c0001t0005g0089 a0001c0001t0005g0145 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1086+1669C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439165 | |||||||
chr1:218439283 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1086+1787G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439283 | |||||||
chr1:218439336 | G | A | 2 | a0001c0001t0003g0255 a0001c0001t0083g0262 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1086+1840G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439336 | |||||||
chr1:218439502 | G | T | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1087-1702G>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439502 | |||||||
chr1:218439606 | C | T | 2 | a0001c0001t0006g0176 a0001c0001t0063g0187 |
2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1087-1598C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218439606 | |||||||
chr1:218440175 | C | T | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1087-1029C>T | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440175 | |||||||
chr1:218440278 | T | A | 7 | a0001c0001t0037g0229 a0001c0001t0050g0168 a0001c0001t0051g0055 others(4): Show |
7 | HG03669.hp1 HG04228.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.1087-926T>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440278 | |||||||
chr1:218440345 | CT | C | 167 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0071 others(164): Show |
170 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.1087-847delT | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218440345 | ||||||
chr1:218440353 | T | C | 1 | a0001c0001t0075g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1087-851T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440353 | |||||||
chr1:218440571 | A | C | 4 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0003g0256 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087-633A>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440571 | |||||||
chr1:218440680 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0197 a0001c0001t0040g0249 |
3 | HG00738.hp1 HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1087-524A>G | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440680 | |||||||
chr1:218440829 | TA | T | 4 | a0001c0001t0001g0077 a0001c0001t0003g0219 a0001c0001t0016g0062 others(1): Show |
4 | HG01169.hp1 HG02486.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087-373delA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218440829 | ||||||
chr1:218440924 | G | GA | 55 | a0001c0001t0006g0088 a0001c0001t0006g0101 a0001c0001t0006g0119 others(52): Show |
56 | HG01109.hp2 HG01243.hp1 HG01258.hp1 others(53): Show |
intron_variant | MODIFIER | c.1087-276dupA | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 218440924 | ||||||
chr1:218440987 | T | C | 1 | a0001c0001t0003g0232 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1087-217T>C | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440987 | |||||||
chr1:218440997 | G | A | 5 | a0001c0001t0021g0221 a0001c0001t0021g0228 a0001c0001t0049g0205 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087-207G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218440997 | |||||||
chr1:218441163 | G | A | 1 | a0001c0001t0009g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1087-41G>A | TGFB2 | ENSG00000092969.12 | transcript | ENST00000366930.9 | protein_coding | 6/6 | chr1 | 218441163 |