Item | Value |
---|---|
geneid | 7490 |
ensemblid | ENSG00000184937.16 |
hgncid | 12796 |
symbol | WT1 |
name | WT1 transcription factor |
refseq_nuc | NM_024426.6 |
refseq_prot | NP_077744.4 |
ensembl_nuc | ENST00000452863.10 |
ensembl_prot | ENSP00000415516.5 |
mane_status | MANE Select |
chr | chr11 |
start | 32387775 |
end | 32435539 |
strand | - |
ver | v1.2 |
region | chr11:32387775-32435539 |
region5000 | chr11:32382775-32440539 |
regionname0 | WT1_chr11_32387775_32435539 |
regionname5000 | WT1_chr11_32382775_32440539 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1566 | 94 | 1 | 15 | 61 | 2 | 15 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0002 | 1/1 | 1566 | 89 | 8 | 25 | 40 | 2 | 12 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0003 | 0/0 | 1566 | 47 | 28 | 8 | 4 | 0 | 7 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0004 | 0/0 | 1566 | 32 | 23 | 3 | 5 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0005 | 0/0 | 1566 | 15 | 3 | 0 | 5 | 0 | 7 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0006 | 0/0 | 1566 | 14 | 1 | 1 | 8 | 0 | 4 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0007 | 0/0 | 1566 | 9 | 1 | 5 | 2 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0008 | 0/0 | 1566 | 7 | 6 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0009 | 0/0 | 1566 | 6 | 6 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0010 | 0/0 | 1566 | 6 | 5 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0011 | 0/0 | 1566 | 3 | 0 | 3 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0012 | 0/0 | 1566 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0013 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0014 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0015 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 | ||
a0001c0016 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | CTGGA others(1561): Show |
chr11 | 32382775 | 32440539 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 3026 | 82 | 1 | 13 | 54 | 2 | 12 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3021): Show |
chr11 | 32382775 | 32440539 |
a0001c0001t0005 | 0/0 | 3025 | 5 | 0 | 0 | 5 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0001t0012 | 0/0 | 3028 | 3 | 0 | 1 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3023): Show |
chr11 | 32382775 | 32440539 |
a0001c0001t0013 | 0/0 | 3026 | 3 | 0 | 1 | 0 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3021): Show |
chr11 | 32382775 | 32440539 |
a0001c0001t0019 | 0/0 | 3026 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3021): Show |
chr11 | 32382775 | 32440539 |
a0001c0002t0001 | 1/1 | 3031 | 73 | 1 | 19 | 38 | 1 | 12 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0002t0003 | 0/0 | 3027 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0002t0004 | 0/0 | 3025 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0002t0007 | 0/0 | 3033 | 4 | 0 | 4 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3028): Show |
chr11 | 32382775 | 32440539 |
a0001c0002t0011 | 0/0 | 3025 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0002t0015 | 0/0 | 3029 | 3 | 0 | 2 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3024): Show |
chr11 | 32382775 | 32440539 |
a0001c0002t0026 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0002t0027 | 0/0 | 3025 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0001 | 0/0 | 3031 | 6 | 1 | 1 | 2 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0002 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3021): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0003 | 0/0 | 3027 | 11 | 2 | 4 | 0 | 0 | 5 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0004 | 0/0 | 3025 | 11 | 11 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0006 | 0/0 | 3027 | 7 | 7 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0009 | 0/0 | 3029 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3024): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0010 | 0/0 | 3029 | 3 | 2 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3024): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0016 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0024 | 0/0 | 3025 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0025 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3016): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0029 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3024): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0031 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3028): Show |
chr11 | 32382775 | 32440539 |
a0001c0003t0032 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0001 | 0/0 | 3031 | 5 | 2 | 2 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0003 | 0/0 | 3027 | 7 | 6 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0004 | 0/0 | 3025 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0006 | 0/0 | 3027 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0007 | 0/0 | 3033 | 6 | 1 | 0 | 5 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3028): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0009 | 0/0 | 3029 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3024): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0017 | 0/0 | 3027 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0018 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0020 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0004t0030 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0005t0002 | 0/0 | 3026 | 6 | 3 | 0 | 2 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3021): Show |
chr11 | 32382775 | 32440539 |
a0001c0005t0005 | 0/0 | 3025 | 8 | 0 | 0 | 2 | 0 | 6 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0005t0022 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0006t0001 | 0/0 | 3031 | 10 | 1 | 0 | 7 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0006t0002 | 0/0 | 3026 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3021): Show |
chr11 | 32382775 | 32440539 |
a0001c0006t0003 | 0/0 | 3027 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0006t0009 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3024): Show |
chr11 | 32382775 | 32440539 |
a0001c0006t0018 | 0/0 | 3031 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0007t0001 | 0/0 | 3031 | 2 | 0 | 2 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0007t0002 | 0/0 | 3026 | 5 | 0 | 3 | 1 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3021): Show |
chr11 | 32382775 | 32440539 |
a0001c0007t0005 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3020): Show |
chr11 | 32382775 | 32440539 |
a0001c0007t0028 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3024): Show |
chr11 | 32382775 | 32440539 |
a0001c0008t0003 | 0/0 | 3027 | 7 | 6 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0009t0008 | 0/0 | 3031 | 5 | 5 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0009t0033 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3024): Show |
chr11 | 32382775 | 32440539 |
a0001c0010t0006 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0010t0008 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0010t0014 | 0/0 | 3033 | 2 | 1 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3028): Show |
chr11 | 32382775 | 32440539 |
a0001c0010t0016 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
a0001c0010t0021 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3016): Show |
chr11 | 32382775 | 32440539 |
a0001c0011t0001 | 0/0 | 3031 | 3 | 0 | 3 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0012t0014 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3028): Show |
chr11 | 32382775 | 32440539 |
a0001c0012t0023 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3024): Show |
chr11 | 32382775 | 32440539 |
a0001c0013t0001 | 0/0 | 3031 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0014t0008 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0015t0001 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3026): Show |
chr11 | 32382775 | 32440539 |
a0001c0016t0016 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | AGGCA others(3022): Show |
chr11 | 32382775 | 32440539 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0005g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0012g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0012g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0012g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0013g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0013g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0013g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0019g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0007g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0007g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0007g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0015g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0015g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0015g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0026g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0027g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0009g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0010g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0016g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0024g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0025g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0029g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0031g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0032g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0006g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0017g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0017g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0020g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0030g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0022g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0018g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0028g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0033g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0014g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0014g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0016g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0021g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0011t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0011t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0011t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0012t0014g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0012t0023g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0013t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0014t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0015t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0016t0016g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | GBR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0100 | EUR | GBR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00408 | hp1 | a0001 | c0007 | t0002 | g0045 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00438 | hp1 | a0001 | c0015 | t0001 | g0046 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00642 | hp1 | a0001 | c0008 | t0003 | g0286 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00733 | hp2 | a0001 | c0003 | t0003 | g0245 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00735 | hp1 | a0001 | c0004 | t0003 | g0017 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00735 | hp2 | a0001 | c0002 | t0007 | g0071 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00741 | hp2 | a0001 | c0004 | t0001 | g0279 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01074 | hp1 | a0001 | c0002 | t0007 | g0087 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01074 | hp2 | a0001 | c0006 | t0018 | g0125 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01099 | hp1 | a0001 | c0003 | t0025 | g0233 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01109 | hp2 | a0001 | c0010 | t0014 | g0268 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0231 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01175 | hp1 | a0001 | c0003 | t0024 | g0232 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01175 | hp2 | a0001 | c0007 | t0001 | g0054 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01243 | hp1 | a0001 | c0007 | t0002 | g0033 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01256 | hp1 | a0001 | c0004 | t0001 | g0281 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01256 | hp2 | a0001 | c0007 | t0001 | g0072 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01261 | hp2 | a0001 | c0003 | t0003 | g0246 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01346 | hp1 | a0001 | c0001 | t0013 | g0174 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01358 | hp1 | a0001 | c0002 | t0015 | g0051 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01358 | hp2 | a0001 | c0002 | t0015 | g0056 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01361 | hp1 | a0001 | c0003 | t0003 | g0243 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01496 | hp1 | a0001 | c0003 | t0010 | g0020 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01884 | hp1 | a0001 | c0005 | t0002 | g0252 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01884 | hp2 | a0001 | c0004 | t0020 | g0301 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01891 | hp1 | a0001 | c0004 | t0003 | g0017 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01891 | hp2 | a0001 | c0004 | t0009 | g0295 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01928 | hp2 | a0001 | c0011 | t0001 | g0024 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01975 | hp1 | a0001 | c0001 | t0012 | g0151 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01975 | hp2 | a0001 | c0011 | t0001 | g0022 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01978 | hp2 | a0001 | c0011 | t0001 | g0023 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01981 | hp2 | a0001 | c0007 | t0002 | g0106 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01993 | hp1 | a0001 | c0002 | t0007 | g0044 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02055 | hp1 | a0001 | c0004 | t0017 | g0282 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02055 | hp2 | a0001 | c0004 | t0003 | g0292 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02129 | hp2 | a0001 | c0005 | t0005 | g0255 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02145 | hp1 | a0001 | c0004 | t0003 | g0272 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02145 | hp2 | a0001 | c0003 | t0016 | g0223 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02148 | hp2 | a0001 | c0007 | t0002 | g0103 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | CDX | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CDX | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02257 | hp1 | a0001 | c0006 | t0001 | g0211 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02257 | hp2 | a0001 | c0003 | t0004 | g0239 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02280 | hp1 | a0001 | c0009 | t0033 | g0305 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02280 | hp2 | a0001 | c0010 | t0021 | g0215 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02300 | hp1 | a0001 | c0003 | t0003 | g0244 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02300 | hp2 | a0001 | c0002 | t0007 | g0086 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02451 | hp1 | a0001 | c0010 | t0006 | g0216 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02451 | hp2 | a0001 | c0003 | t0010 | g0019 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02572 | hp1 | a0001 | c0002 | t0011 | g0030 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02572 | hp2 | a0001 | c0009 | t0008 | g0035 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02602 | hp2 | a0001 | c0006 | t0001 | g0150 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02622 | hp1 | a0001 | c0008 | t0003 | g0284 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02622 | hp2 | a0001 | c0003 | t0004 | g0240 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02630 | hp1 | a0001 | c0008 | t0003 | g0288 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02630 | hp2 | a0001 | c0014 | t0008 | g0036 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02647 | hp1 | a0001 | c0003 | t0004 | g0228 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02647 | hp2 | a0001 | c0004 | t0007 | g0285 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0092 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02683 | hp2 | a0001 | c0001 | t0019 | g0021 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02717 | hp1 | a0001 | c0004 | t0004 | g0274 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02717 | hp2 | a0001 | c0002 | t0011 | g0027 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02723 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02723 | hp2 | a0001 | c0008 | t0003 | g0291 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0230 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02818 | hp1 | a0001 | c0003 | t0010 | g0018 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02818 | hp2 | a0001 | c0004 | t0017 | g0278 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02886 | hp1 | a0001 | c0004 | t0006 | g0016 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02886 | hp2 | a0001 | c0004 | t0004 | g0273 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02895 | hp1 | a0001 | c0003 | t0004 | g0238 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02895 | hp2 | a0001 | c0003 | t0006 | g0225 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02896 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02896 | hp2 | a0001 | c0012 | t0023 | g0209 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0028 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02897 | hp2 | a0001 | c0003 | t0006 | g0226 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02965 | hp1 | a0001 | c0010 | t0014 | g0270 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02965 | hp2 | a0001 | c0004 | t0018 | g0294 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02970 | hp1 | a0001 | c0003 | t0004 | g0012 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02970 | hp2 | a0001 | c0007 | t0028 | g0034 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02976 | hp1 | a0001 | c0004 | t0030 | g0300 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02976 | hp2 | a0001 | c0004 | t0009 | g0293 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03017 | hp1 | a0001 | c0013 | t0001 | g0025 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03017 | hp2 | a0001 | c0003 | t0003 | g0237 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03098 | hp1 | a0001 | c0009 | t0008 | g0031 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03098 | hp2 | a0001 | c0009 | t0008 | g0004 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03130 | hp2 | a0001 | c0002 | t0011 | g0026 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0214 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03139 | hp2 | a0001 | c0003 | t0006 | g0224 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03195 | hp1 | a0001 | c0003 | t0006 | g0218 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03209 | hp1 | a0001 | c0003 | t0004 | g0014 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03209 | hp2 | a0001 | c0004 | t0006 | g0016 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03225 | hp1 | a0001 | c0004 | t0009 | g0287 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03225 | hp2 | a0001 | c0003 | t0006 | g0219 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03239 | hp2 | a0001 | c0004 | t0001 | g0283 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03453 | hp1 | a0001 | c0008 | t0003 | g0296 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0069 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03486 | hp1 | a0001 | c0009 | t0008 | g0032 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03486 | hp2 | a0001 | c0010 | t0008 | g0217 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03490 | hp2 | a0001 | c0005 | t0005 | g0266 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03491 | hp1 | a0001 | c0001 | t0013 | g0141 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03491 | hp2 | a0001 | c0003 | t0003 | g0250 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03492 | hp1 | a0001 | c0001 | t0013 | g0147 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03516 | hp1 | a0001 | c0003 | t0006 | g0251 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03516 | hp2 | a0001 | c0002 | t0003 | g0060 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03540 | hp1 | a0001 | c0004 | t0006 | g0290 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03540 | hp2 | a0001 | c0009 | t0008 | g0004 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03579 | hp1 | a0001 | c0003 | t0004 | g0012 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03579 | hp2 | a0001 | c0003 | t0004 | g0014 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03654 | hp1 | a0001 | c0005 | t0005 | g0258 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03654 | hp2 | a0001 | c0003 | t0003 | g0248 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03688 | hp2 | a0001 | c0003 | t0003 | g0247 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03704 | hp1 | a0001 | c0007 | t0002 | g0041 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03704 | hp2 | a0001 | c0005 | t0005 | g0257 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03710 | hp2 | a0001 | c0006 | t0002 | g0180 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03927 | hp1 | a0001 | c0005 | t0005 | g0259 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03942 | hp2 | a0001 | c0005 | t0005 | g0254 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04115 | hp2 | a0001 | c0005 | t0002 | g0264 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04184 | hp1 | a0001 | c0006 | t0001 | g0113 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04199 | hp1 | a0001 | c0006 | t0003 | g0169 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0267 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04204 | hp1 | a0001 | c0005 | t0005 | g0260 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04228 | hp2 | a0001 | c0003 | t0003 | g0242 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18522 | hp1 | a0001 | c0003 | t0032 | g0229 | AFR | YRI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | YRI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18940 | hp1 | a0001 | c0005 | t0002 | g0241 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18942 | hp1 | a0001 | c0005 | t0002 | g0262 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18942 | hp2 | a0001 | c0004 | t0007 | g0276 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18947 | hp1 | a0001 | c0004 | t0007 | g0303 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0263 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18953 | hp2 | a0001 | c0002 | t0026 | g0094 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18956 | hp1 | a0001 | c0004 | t0007 | g0304 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18960 | hp2 | a0001 | c0002 | t0015 | g0053 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18961 | hp2 | a0001 | c0006 | t0009 | g0177 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18963 | hp2 | a0001 | c0006 | t0001 | g0167 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18964 | hp1 | a0001 | c0004 | t0007 | g0275 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18973 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18979 | hp2 | a0001 | c0004 | t0007 | g0277 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18982 | hp2 | a0001 | c0006 | t0001 | g0163 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18985 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18987 | hp2 | a0001 | c0003 | t0009 | g0234 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18991 | hp1 | a0001 | c0005 | t0022 | g0265 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18992 | hp2 | a0001 | c0001 | t0012 | g0195 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18995 | hp1 | a0001 | c0006 | t0001 | g0145 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19003 | hp2 | a0001 | c0006 | t0001 | g0198 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19005 | hp2 | a0001 | c0006 | t0001 | g0197 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19010 | hp1 | a0001 | c0003 | t0009 | g0235 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19030 | hp1 | a0001 | c0012 | t0014 | g0210 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19030 | hp2 | a0001 | c0003 | t0006 | g0222 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19043 | hp1 | a0001 | c0003 | t0031 | g0249 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19043 | hp2 | a0001 | c0008 | t0003 | g0280 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19056 | hp2 | a0001 | c0005 | t0005 | g0261 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19063 | hp2 | a0001 | c0001 | t0012 | g0200 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0256 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19084 | hp1 | a0001 | c0006 | t0001 | g0153 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19240 | hp1 | a0001 | c0004 | t0004 | g0297 | AFR | YRI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19240 | hp2 | a0001 | c0004 | t0003 | g0299 | AFR | YRI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20129 | hp1 | a0001 | c0005 | t0002 | g0212 | AFR | ASW | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0227 | AFR | ASW | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0139 | EUR | TSI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20752 | hp2 | a0001 | c0002 | t0027 | g0091 | EUR | TSI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | GIH | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | GIH | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02109 | hp1 | a0001 | c0004 | t0003 | g0271 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0253 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02486 | hp1 | a0001 | c0010 | t0016 | g0269 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02486 | hp2 | a0001 | c0004 | t0003 | g0302 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02559 | hp1 | a0001 | c0003 | t0003 | g0213 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02559 | hp2 | a0001 | c0003 | t0029 | g0220 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03471 | hp1 | a0001 | c0016 | t0016 | g0298 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03471 | hp2 | a0001 | c0008 | t0003 | g0289 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18955 | hp1 | a0001 | c0007 | t0005 | g0043 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18955 | hp2 | a0001 | c0006 | t0001 | g0115 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA21309 | hp1 | a0001 | c0005 | t0002 | g0221 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA21309 | hp2 | a0001 | c0003 | t0004 | g0236 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0089 | REF | REF | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0105 | REF | REF | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:32392048 | C | T | 1 | a0001c0014 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.1371G>A | p.Gln457Gln | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/10 | 1550/3031 | 1371/1569 | 457/522 | chr11 | 32392048 | |||
chr11:32396399 | T | C | 4 | a0001c0001 a0001c0005 a0001c0007 others(1): Show |
125 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(122): Show |
synonymous_variant | LOW | c.1122A>G | p.Arg374Arg | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/10 | 1301/3031 | 1122/1569 | 374/522 | chr11 | 32396399 | |||
chr11:32399987 | T | C | 5 | a0001c0009 a0001c0010 a0001c0012 others(2): Show |
16 | HG01109.hp2 HG02280.hp1 HG02280.hp2 others(13): Show |
synonymous_variant | LOW | c.1074A>G | p.Gln358Gln | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/10 | 1253/3031 | 1074/1569 | 358/522 | chr11 | 32399987 | |||
chr11:32428585 | G | A | 1 | a0001c0015 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.696C>T | p.Ser232Ser | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/10 | 875/3031 | 696/1569 | 232/522 | chr11 | 32428585 | |||
chr11:32434752 | G | A | 3 | a0001c0004 a0001c0008 a0001c0016 |
40 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(37): Show |
synonymous_variant | LOW | c.609C>T | p.Asn203Asn | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 788/3031 | 609/1569 | 203/522 | chr11 | 32434752 | |||
chr11:32434848 | G | T | 1 | a0001c0013 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.513C>A | p.Gly171Gly | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 692/3031 | 513/1569 | 171/522 | chr11 | 32434848 | |||
chr11:32435016 | G | A | 3 | a0001c0001 a0001c0006 a0001c0012 |
110 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(107): Show |
synonymous_variant | LOW | c.345C>T | p.Pro115Pro | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 524/3031 | 345/1569 | 115/522 | chr11 | 32435016 | |||
chr11:32435148 | C | A | 6 | a0001c0003 a0001c0004 a0001c0005 others(3): Show |
108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
synonymous_variant | LOW | c.213G>T | p.Pro71Pro | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 392/3031 | 213/1569 | 71/522 | chr11 | 32435148 | |||
chr11:32435180 | G | T | 1 | a0001c0011 | 3 | HG01928.hp2 HG01975.hp2 HG01978.hp2 |
synonymous_variant | LOW | c.181C>A | p.Arg61Arg | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 360/3031 | 181/1569 | 61/522 | chr11 | 32435180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:32387849 | T | C | 2 | a0001c0002t0011 a0001c0004t0020 |
4 | HG01884.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1209A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1209 | chr11 | 32387849 | ||||||
chr11:32387926 | T | A | 1 | a0001c0001t0013 | 3 | HG01346.hp1 HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1132A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1132 | chr11 | 32387926 | ||||||
chr11:32387960 | G | A | 4 | a0001c0003t0016 a0001c0010t0016 a0001c0010t0021 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1098C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1098 | chr11 | 32387960 | ||||||
chr11:32388003 | A | AAC | 5 | a0001c0002t0007 a0001c0003t0031 a0001c0004t0007 others(2): Show |
14 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1054dupGT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1054 | chr11 | 32388003 | ||||||
chr11:32388003 | AAC | A | 9 | a0001c0002t0015 a0001c0003t0009 a0001c0003t0010 others(6): Show |
16 | HG01358.hp1 HG01358.hp2 HG01496.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1054delGT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1053 | chr11 | 32388003 | ||||||
chr11:32388003 | AACAC | A | 14 | a0001c0001t0012 a0001c0002t0003 a0001c0002t0026 others(11): Show |
48 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1051_*1054delGTGT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1051 | chr11 | 32388003 | ||||||
chr11:32388003 | AACACAC | A | 19 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(16): Show |
137 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1049_*1054delGTGT others(2): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1049 | chr11 | 32388003 | ||||||
chr11:32388003 | AACACACA others(3): Show |
A | 2 | a0001c0003t0025 a0001c0010t0021 |
2 | HG01099.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1045_*1054delGTGT others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1045 | chr11 | 32388003 | ||||||
chr11:32388079 | A | AT | 8 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0013 others(5): Show |
102 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*978dupA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 978 | chr11 | 32388079 | ||||||
chr11:32388155 | C | T | 1 | a0001c0007t0028 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*903G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 903 | chr11 | 32388155 | ||||||
chr11:32388194 | A | C | 4 | a0001c0003t0016 a0001c0010t0016 a0001c0010t0021 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*864T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 864 | chr11 | 32388194 | ||||||
chr11:32388223 | T | C | 2 | a0001c0003t0024 a0001c0003t0025 |
2 | HG01099.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*835A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 835 | chr11 | 32388223 | ||||||
chr11:32388238 | C | G | 3 | a0001c0002t0004 a0001c0003t0004 a0001c0004t0004 |
16 | HG02257.hp2 HG02622.hp2 HG02647.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*820G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 820 | chr11 | 32388238 | ||||||
chr11:32388456 | T | C | 47 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(44): Show |
205 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*602A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 602 | chr11 | 32388456 | ||||||
chr11:32388516 | C | T | 1 | a0001c0004t0030 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*542G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 542 | chr11 | 32388516 | ||||||
chr11:32388713 | C | T | 1 | a0001c0002t0011 | 3 | HG02572.hp1 HG02717.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*345G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 345 | chr11 | 32388713 | ||||||
chr11:32388791 | C | G | 49 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(46): Show |
210 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*267G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 267 | chr11 | 32388791 | ||||||
chr11:32388834 | T | C | 13 | a0001c0002t0003 a0001c0003t0003 a0001c0003t0009 others(10): Show |
39 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*224A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 224 | chr11 | 32388834 | ||||||
chr11:32388920 | C | T | 1 | a0001c0004t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 138 | chr11 | 32388920 | ||||||
chr11:32388970 | T | C | 16 | a0001c0002t0003 a0001c0003t0003 a0001c0003t0009 others(13): Show |
44 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*88A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 88 | chr11 | 32388970 | ||||||
chr11:32389042 | C | A | 3 | a0001c0003t0016 a0001c0010t0016 a0001c0016t0016 |
3 | HG02145.hp2 HG02486.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*16G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 16 | chr11 | 32389042 | ||||||
chr11:32435420 | G | T | 1 | a0001c0001t0019 | 1 | HG02683.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 60 | chr11 | 32435420 | ||||||
chr11:32435423 | G | A | 1 | a0001c0009t0033 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 63 | chr11 | 32435423 | ||||||
chr11:32435435 | G | T | 1 | a0001c0003t0010 | 3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 75 | chr11 | 32435435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:32389189 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1448-10G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389189 | |||||||
chr11:32389228 | A | G | 176 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(173): Show |
184 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1448-49T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389228 | |||||||
chr11:32389408 | C | A | 2 | a0001c0005t0005g0254 a0001c0005t0005g0266 |
2 | HG03490.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1448-229G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389408 | |||||||
chr11:32389554 | G | A | 48 | a0001c0002t0001g0049 a0001c0002t0003g0060 a0001c0002t0003g0069 others(45): Show |
49 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1448-375C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389554 | |||||||
chr11:32389694 | T | A | 94 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(91): Show |
97 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1448-515A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389694 | |||||||
chr11:32389795 | G | C | 1 | a0001c0003t0004g0228 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1448-616C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389795 | |||||||
chr11:32389826 | C | G | 2 | a0001c0003t0024g0232 a0001c0003t0025g0233 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1448-647G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389826 | |||||||
chr11:32389874 | T | C | 2 | a0001c0003t0024g0232 a0001c0003t0025g0233 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1448-695A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389874 | |||||||
chr11:32389902 | A | G | 1 | a0001c0002t0001g0078 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1448-723T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389902 | |||||||
chr11:32390089 | G | T | 4 | a0001c0010t0014g0268 a0001c0010t0014g0270 a0001c0012t0014g0210 others(1): Show |
4 | HG01109.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1448-910C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390089 | |||||||
chr11:32390414 | C | T | 4 | a0001c0003t0016g0223 a0001c0010t0016g0269 a0001c0010t0021g0215 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1448-1235G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390414 | |||||||
chr11:32390458 | C | G | 1 | a0001c0004t0001g0279 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1448-1279G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390458 | |||||||
chr11:32390483 | A | G | 4 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0010t0008g0217 others(1): Show |
5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1448-1304T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390483 | |||||||
chr11:32390487 | C | T | 3 | a0001c0004t0006g0016 a0001c0004t0006g0290 a0001c0010t0006g0216 |
4 | HG02451.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1448-1308G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390487 | |||||||
chr11:32390494 | T | C | 49 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(46): Show |
50 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1448-1315A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390494 | |||||||
chr11:32390520 | G | A | 10 | a0001c0001t0002g0011 a0001c0001t0002g0134 a0001c0001t0002g0165 others(7): Show |
11 | HG00642.hp2 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1448-1341C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390520 | |||||||
chr11:32390952 | A | T | 1 | a0001c0002t0001g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1447+1020T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390952 | |||||||
chr11:32390971 | TTGTTTG | T | 44 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(41): Show |
45 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1447+995_1447+1000 others(9): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390971 | |||||||
chr11:32390973 | GTTTGT | G | 133 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(130): Show |
140 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1447+994_1447+998d others(7): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390973 | |||||||
chr11:32390978 | T | G | 44 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(41): Show |
45 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1447+994A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390978 | |||||||
chr11:32391089 | C | T | 1 | a0001c0009t0033g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1447+883G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391089 | |||||||
chr11:32391090 | G | A | 4 | a0001c0003t0016g0223 a0001c0010t0016g0269 a0001c0010t0021g0215 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447+882C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391090 | |||||||
chr11:32391141 | T | C | 1 | a0001c0001t0002g0127 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1447+831A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391141 | |||||||
chr11:32391237 | A | AACC | 44 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(41): Show |
45 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1447+734_1447+735i others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391237 | |||||||
chr11:32391262 | A | G | 1 | a0001c0001t0002g0143 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1447+710T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391262 | |||||||
chr11:32391277 | C | T | 4 | a0001c0003t0016g0223 a0001c0010t0016g0269 a0001c0010t0021g0215 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447+695G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391277 | |||||||
chr11:32391337 | T | C | 4 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0010t0008g0217 others(1): Show |
5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447+635A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391337 | |||||||
chr11:32391361 | A | G | 3 | a0001c0011t0001g0022 a0001c0011t0001g0023 a0001c0011t0001g0024 |
3 | HG01928.hp2 HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1447+611T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391361 | |||||||
chr11:32391523 | C | T | 2 | a0001c0002t0003g0060 a0001c0002t0003g0069 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1447+449G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391523 | |||||||
chr11:32391572 | A | G | 1 | a0001c0004t0003g0292 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1447+400T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391572 | |||||||
chr11:32392096 | C | T | 1 | a0001c0003t0003g0243 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1355-32G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 8/9 | chr11 | 32392096 | |||||||
chr11:32392151 | C | T | 10 | a0001c0001t0002g0011 a0001c0001t0002g0134 a0001c0001t0002g0165 others(7): Show |
11 | HG00642.hp2 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1355-87G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 8/9 | chr11 | 32392151 | |||||||
chr11:32392787 | G | T | 35 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(32): Show |
36 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1265-32C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392787 | |||||||
chr11:32392896 | A | C | 4 | a0001c0010t0014g0268 a0001c0010t0014g0270 a0001c0012t0014g0210 others(1): Show |
4 | HG01109.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265-141T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392896 | |||||||
chr11:32392928 | G | A | 4 | a0001c0003t0010g0018 a0001c0003t0010g0019 a0001c0003t0010g0020 others(1): Show |
4 | HG01496.hp1 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1265-173C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392928 | |||||||
chr11:32392936 | G | C | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1265-181C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392936 | |||||||
chr11:32392972 | T | TA | 44 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(41): Show |
49 | HG00558.hp1 HG02129.hp2 HG02257.hp2 others(46): Show |
intron_variant | MODIFIER | c.1265-218dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392972 | |||||||
chr11:32393004 | G | A | 14 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(11): Show |
15 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(12): Show |
intron_variant | MODIFIER | c.1265-249C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393004 | |||||||
chr11:32393041 | A | G | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1265-286T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393041 | |||||||
chr11:32393100 | C | T | 7 | a0001c0003t0006g0218 a0001c0003t0006g0219 a0001c0003t0006g0222 others(4): Show |
7 | HG02895.hp2 HG02897.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1265-345G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393100 | |||||||
chr11:32393101 | G | A | 10 | a0001c0001t0002g0122 a0001c0001t0002g0130 a0001c0001t0002g0131 others(7): Show |
10 | HG00558.hp2 HG00621.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1265-346C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393101 | |||||||
chr11:32393330 | G | T | 1 | a0001c0006t0001g0211 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1265-575C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393330 | |||||||
chr11:32393406 | C | T | 3 | a0001c0001t0002g0120 a0001c0001t0002g0186 a0001c0001t0002g0207 |
3 | NA18947.hp2 NA18950.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1265-651G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393406 | |||||||
chr11:32393564 | CA | C | 137 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(134): Show |
141 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1265-810delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393564 | |||||||
chr11:32393763 | A | G | 1 | a0001c0005t0005g0266 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1265-1008T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393763 | |||||||
chr11:32393929 | G | A | 2 | a0001c0005t0005g0258 a0001c0005t0005g0260 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1265-1174C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393929 | |||||||
chr11:32393941 | A | G | 109 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(106): Show |
112 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1265-1186T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393941 | |||||||
chr11:32393983 | C | T | 35 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(32): Show |
36 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1265-1228G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393983 | |||||||
chr11:32394140 | G | A | 1 | a0001c0010t0021g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1265-1385C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394140 | |||||||
chr11:32394145 | C | T | 4 | a0001c0003t0010g0018 a0001c0003t0010g0019 a0001c0003t0010g0020 others(1): Show |
4 | HG01496.hp1 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1265-1390G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394145 | |||||||
chr11:32394146 | G | A | 1 | a0001c0005t0002g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1265-1391C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394146 | |||||||
chr11:32394276 | T | C | 14 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(11): Show |
15 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(12): Show |
intron_variant | MODIFIER | c.1265-1521A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394276 | |||||||
chr11:32394339 | C | T | 2 | a0001c0002t0001g0052 a0001c0002t0001g0076 |
2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1265-1584G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394339 | |||||||
chr11:32394391 | T | C | 4 | a0001c0003t0016g0223 a0001c0010t0016g0269 a0001c0010t0021g0215 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265-1636A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394391 | |||||||
chr11:32394539 | C | T | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1264+1718G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394539 | |||||||
chr11:32395042 | A | T | 4 | a0001c0003t0016g0223 a0001c0010t0016g0269 a0001c0010t0021g0215 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264+1215T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395042 | |||||||
chr11:32395329 | G | A | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(99): Show |
105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1264+928C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395329 | |||||||
chr11:32395438 | C | T | 2 | a0001c0003t0003g0242 a0001c0007t0028g0034 |
2 | HG02970.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1264+819G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395438 | |||||||
chr11:32395477 | C | CT | 6 | a0001c0001t0012g0195 a0001c0002t0001g0090 a0001c0002t0001g0092 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264+779dupA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395477 | |||||||
chr11:32395514 | C | T | 97 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(94): Show |
100 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1264+743G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395514 | |||||||
chr11:32395622 | C | T | 1 | a0001c0007t0002g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1264+635G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395622 | |||||||
chr11:32395633 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1264+624A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395633 | |||||||
chr11:32395687 | C | T | 3 | a0001c0010t0014g0270 a0001c0012t0014g0210 a0001c0012t0023g0209 |
3 | HG02896.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1264+570G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395687 | |||||||
chr11:32395708 | C | T | 1 | a0001c0016t0016g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1264+549G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395708 | |||||||
chr11:32395761 | CT | C | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(99): Show |
105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1264+495delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395761 | |||||||
chr11:32395802 | C | T | 1 | a0001c0005t0002g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1264+455G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395802 | |||||||
chr11:32395886 | A | G | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(99): Show |
105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1264+371T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395886 | |||||||
chr11:32395901 | G | A | 31 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(28): Show |
35 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(32): Show |
intron_variant | MODIFIER | c.1264+356C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395901 | |||||||
chr11:32395980 | A | C | 57 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(54): Show |
60 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1264+277T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395980 | |||||||
chr11:32396122 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1264+135T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32396122 | |||||||
chr11:32396123 | A | T | 101 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(98): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1264+134T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32396123 | |||||||
chr11:32396144 | A | C | 2 | a0001c0003t0024g0232 a0001c0003t0025g0233 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1264+113T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32396144 | |||||||
chr11:32396567 | C | T | 9 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0003t0002g0227 others(6): Show |
11 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1114-160G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32396567 | |||||||
chr11:32396688 | A | G | 1 | a0001c0003t0010g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1114-281T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32396688 | |||||||
chr11:32396880 | A | G | 1 | a0001c0009t0033g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1114-473T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32396880 | |||||||
chr11:32396931 | G | A | 7 | a0001c0010t0014g0268 a0001c0010t0014g0270 a0001c0010t0016g0269 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114-524C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32396931 | |||||||
chr11:32397059 | T | A | 100 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(97): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1114-652A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397059 | |||||||
chr11:32397345 | C | G | 7 | a0001c0009t0008g0004 a0001c0009t0008g0031 a0001c0009t0008g0032 others(4): Show |
8 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114-938G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397345 | |||||||
chr11:32397413 | T | C | 2 | a0001c0009t0008g0031 a0001c0009t0008g0032 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1114-1006A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397413 | |||||||
chr11:32397482 | A | AT | 147 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(144): Show |
154 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.1114-1076dupA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397482 | |||||||
chr11:32397482 | A | ATT | 33 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0003t0001g0230 others(30): Show |
36 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1114-1077_1114-107 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397482 | |||||||
chr11:32397493 | T | G | 1 | a0001c0004t0007g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1114-1086A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397493 | |||||||
chr11:32397500 | G | A | 4 | a0001c0001t0002g0133 a0001c0001t0002g0164 a0001c0001t0002g0168 others(1): Show |
4 | HG02602.hp1 HG02683.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-1093C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397500 | |||||||
chr11:32397504 | G | A | 3 | a0001c0001t0002g0137 a0001c0001t0002g0139 a0001c0001t0002g0162 |
3 | HG03239.hp1 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1114-1097C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397504 | |||||||
chr11:32397606 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1114-1199G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397606 | |||||||
chr11:32397806 | A | T | 100 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(97): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1114-1399T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397806 | |||||||
chr11:32398230 | C | T | 3 | a0001c0003t0004g0236 a0001c0003t0004g0239 a0001c0003t0004g0240 |
3 | HG02257.hp2 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1113+1718G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398230 | |||||||
chr11:32398235 | C | T | 4 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+1713G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398235 | |||||||
chr11:32398349 | G | A | 15 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(12): Show |
16 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.1113+1599C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398349 | |||||||
chr11:32398505 | T | C | 3 | a0001c0003t0009g0234 a0001c0003t0009g0235 a0001c0006t0009g0177 |
3 | NA18961.hp2 NA18987.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1113+1443A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398505 | |||||||
chr11:32398669 | A | T | 2 | a0001c0005t0002g0212 a0001c0005t0002g0252 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1113+1279T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398669 | |||||||
chr11:32398674 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1113+1274A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398674 | |||||||
chr11:32398773 | A | T | 8 | a0001c0003t0006g0218 a0001c0003t0006g0219 a0001c0003t0006g0222 others(5): Show |
8 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+1175T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398773 | |||||||
chr11:32398790 | A | G | 1 | a0001c0002t0001g0062 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1113+1158T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398790 | |||||||
chr11:32398946 | G | A | 100 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(97): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1113+1002C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398946 | |||||||
chr11:32398971 | AC | A | 11 | a0001c0003t0006g0218 a0001c0003t0006g0219 a0001c0003t0006g0222 others(8): Show |
12 | HG02145.hp2 HG02451.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+976delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398971 | |||||||
chr11:32399016 | C | T | 1 | a0001c0010t0006g0216 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1113+932G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399016 | |||||||
chr11:32399024 | T | C | 104 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(101): Show |
107 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1113+924A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399024 | |||||||
chr11:32399025 | G | A | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+923C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399025 | |||||||
chr11:32399086 | G | A | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1113+862C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399086 | |||||||
chr11:32399153 | T | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+795A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399153 | |||||||
chr11:32399348 | C | T | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1113+600G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399348 | |||||||
chr11:32399354 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+594A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399354 | |||||||
chr11:32399429 | A | G | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+519T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399429 | |||||||
chr11:32399444 | T | C | 1 | a0001c0001t0002g0178 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1113+504A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399444 | |||||||
chr11:32399727 | C | G | 1 | a0001c0004t0020g0301 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1113+221G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399727 | |||||||
chr11:32399727 | C | T | 7 | a0001c0009t0008g0004 a0001c0009t0008g0031 a0001c0009t0008g0032 others(4): Show |
8 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+221G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399727 | |||||||
chr11:32400105 | T | C | 1 | a0001c0004t0020g0301 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1017-61A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400105 | |||||||
chr11:32400108 | T | C | 7 | a0001c0002t0001g0047 a0001c0002t0001g0063 a0001c0002t0001g0068 others(4): Show |
7 | HG00621.hp2 HG02015.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017-64A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400108 | |||||||
chr11:32400291 | C | T | 1 | a0001c0005t0002g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1017-247G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400291 | |||||||
chr11:32400295 | G | T | 1 | a0001c0002t0011g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1017-251C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400295 | |||||||
chr11:32400431 | G | A | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
99 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1017-387C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400431 | |||||||
chr11:32400446 | G | A | 15 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(12): Show |
16 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.1017-402C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400446 | |||||||
chr11:32400526 | G | A | 1 | a0001c0001t0002g0160 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1017-482C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400526 | |||||||
chr11:32400646 | C | T | 3 | a0001c0010t0014g0270 a0001c0012t0014g0210 a0001c0012t0023g0209 |
3 | HG02896.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1017-602G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400646 | |||||||
chr11:32400740 | C | T | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1017-696G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400740 | |||||||
chr11:32400966 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1017-922A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400966 | |||||||
chr11:32401178 | G | T | 34 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(31): Show |
35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1017-1134C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401178 | |||||||
chr11:32401274 | T | G | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1017-1230A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401274 | |||||||
chr11:32401472 | G | A | 7 | a0001c0008t0003g0280 a0001c0008t0003g0284 a0001c0008t0003g0286 others(4): Show |
7 | HG00642.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017-1428C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401472 | |||||||
chr11:32401505 | CG | C | 148 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(145): Show |
153 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1017-1462delC | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401505 | |||||||
chr11:32401507 | G | T | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-1463C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401507 | |||||||
chr11:32401523 | G | T | 1 | a0001c0006t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1017-1479C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401523 | |||||||
chr11:32401653 | C | A | 11 | a0001c0003t0006g0218 a0001c0003t0006g0219 a0001c0003t0006g0222 others(8): Show |
12 | HG02145.hp2 HG02451.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017-1609G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401653 | |||||||
chr11:32401654 | C | T | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-1610G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401654 | |||||||
chr11:32401827 | A | G | 32 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(29): Show |
36 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(33): Show |
intron_variant | MODIFIER | c.1017-1783T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401827 | |||||||
chr11:32401906 | C | T | 1 | a0001c0003t0003g0247 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1017-1862G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401906 | |||||||
chr11:32401962 | G | A | 3 | a0001c0010t0014g0270 a0001c0012t0014g0210 a0001c0012t0023g0209 |
3 | HG02896.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1017-1918C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401962 | |||||||
chr11:32402045 | G | C | 1 | a0001c0004t0020g0301 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1017-2001C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402045 | |||||||
chr11:32402117 | G | A | 1 | a0001c0005t0002g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1017-2073C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402117 | |||||||
chr11:32402206 | T | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-2162A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402206 | |||||||
chr11:32402302 | C | A | 1 | a0001c0012t0014g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1017-2258G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402302 | |||||||
chr11:32402368 | A | G | 1 | a0001c0005t0005g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1017-2324T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402368 | |||||||
chr11:32402580 | C | G | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-2536G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402580 | |||||||
chr11:32402590 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1017-2546C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402590 | |||||||
chr11:32402750 | A | C | 1 | a0001c0008t0003g0291 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1017-2706T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402750 | |||||||
chr11:32402750 | A | T | 141 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(138): Show |
145 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1017-2706T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402750 | |||||||
chr11:32402843 | C | A | 57 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(54): Show |
62 | HG01099.hp1 HG01109.hp2 HG01169.hp2 others(59): Show |
intron_variant | MODIFIER | c.1017-2799G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402843 | |||||||
chr11:32402843 | C | G | 132 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(129): Show |
136 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1017-2799G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402843 | |||||||
chr11:32402940 | G | C | 1 | a0001c0004t0020g0301 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1017-2896C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402940 | |||||||
chr11:32403058 | T | C | 184 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(181): Show |
193 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.1017-3014A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403058 | |||||||
chr11:32403278 | C | G | 5 | a0001c0002t0001g0090 a0001c0002t0001g0092 a0001c0002t0001g0096 others(2): Show |
5 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017-3234G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403278 | |||||||
chr11:32403329 | A | C | 1 | a0001c0002t0001g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1017-3285T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403329 | |||||||
chr11:32403555 | C | A | 1 | a0001c0004t0018g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1017-3511G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403555 | |||||||
chr11:32403572 | CT | C | 20 | a0001c0001t0002g0120 a0001c0002t0001g0102 a0001c0003t0010g0018 others(17): Show |
21 | HG01109.hp2 HG01169.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1017-3529delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403572 | |||||||
chr11:32403572 | CTT | C | 111 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(108): Show |
115 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1017-3530_1017-352 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403572 | |||||||
chr11:32403572 | CTTT | C | 24 | a0001c0001t0002g0178 a0001c0001t0002g0186 a0001c0001t0012g0195 others(21): Show |
24 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.1017-3531_1017-352 others(7): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403572 | |||||||
chr11:32403601 | G | A | 1 | a0001c0002t0001g0085 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1017-3557C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403601 | |||||||
chr11:32403614 | G | A | 2 | a0001c0003t0002g0227 a0001c0003t0004g0013 |
3 | HG02723.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1017-3570C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403614 | |||||||
chr11:32403736 | G | A | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-3692C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403736 | |||||||
chr11:32403762 | A | C | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-3718T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403762 | |||||||
chr11:32403951 | ACTCT | A | 5 | a0001c0003t0003g0213 a0001c0003t0003g0214 a0001c0003t0031g0249 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017-3911_1017-390 others(8): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403951 | |||||||
chr11:32404101 | TC | T | 32 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(29): Show |
36 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(33): Show |
intron_variant | MODIFIER | c.1017-4058delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404101 | |||||||
chr11:32404195 | G | A | 7 | a0001c0003t0003g0237 a0001c0003t0003g0242 a0001c0003t0003g0250 others(4): Show |
7 | HG03017.hp2 HG03491.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017-4151C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404195 | |||||||
chr11:32404252 | G | C | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-4208C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404252 | |||||||
chr11:32404268 | C | CA | 11 | a0001c0002t0001g0048 a0001c0002t0001g0055 a0001c0002t0001g0095 others(8): Show |
12 | HG00558.hp1 HG01099.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1017-4225dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404268 | |||||||
chr11:32404268 | CA | C | 62 | a0001c0001t0002g0148 a0001c0001t0002g0165 a0001c0001t0002g0207 others(59): Show |
66 | HG01109.hp2 HG01496.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.1017-4225delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404268 | |||||||
chr11:32404268 | CAA | C | 124 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(121): Show |
128 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1017-4226_1017-422 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404268 | |||||||
chr11:32404316 | T | C | 1 | a0001c0006t0002g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1017-4272A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404316 | |||||||
chr11:32404457 | G | T | 2 | a0001c0007t0001g0054 a0001c0007t0001g0072 |
2 | HG01175.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1017-4413C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404457 | |||||||
chr11:32404563 | C | T | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-4519G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404563 | |||||||
chr11:32404608 | C | A | 32 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(29): Show |
36 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(33): Show |
intron_variant | MODIFIER | c.1017-4564G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404608 | |||||||
chr11:32404923 | G | A | 1 | a0001c0004t0001g0279 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1017-4879C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404923 | |||||||
chr11:32405023 | A | G | 2 | a0001c0002t0001g0084 a0001c0002t0001g0095 |
2 | HG00558.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1017-4979T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405023 | |||||||
chr11:32405077 | T | A | 1 | a0001c0001t0002g0172 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1017-5033A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405077 | |||||||
chr11:32405130 | A | T | 1 | a0001c0004t0004g0274 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1017-5086T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405130 | |||||||
chr11:32405158 | C | T | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-5114G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405158 | |||||||
chr11:32405323 | G | A | 2 | a0001c0004t0004g0273 a0001c0004t0004g0274 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1017-5279C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405323 | |||||||
chr11:32405376 | G | A | 1 | a0001c0002t0007g0087 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1017-5332C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405376 | |||||||
chr11:32405407 | C | G | 130 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(127): Show |
134 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1017-5363G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405407 | |||||||
chr11:32405455 | A | C | 5 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0009t0033g0305 others(2): Show |
6 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017-5411T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405455 | |||||||
chr11:32405490 | A | G | 95 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(92): Show |
98 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1017-5446T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405490 | |||||||
chr11:32405510 | T | A | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-5466A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405510 | |||||||
chr11:32405634 | C | CAT | 179 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(176): Show |
187 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.1017-5591_1017-559 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405634 | |||||||
chr11:32405768 | T | A | 1 | a0001c0001t0002g0178 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1017-5724A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405768 | |||||||
chr11:32405816 | A | G | 1 | a0001c0002t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1017-5772T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405816 | |||||||
chr11:32405821 | G | A | 2 | a0001c0011t0001g0023 a0001c0011t0001g0024 |
2 | HG01928.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1017-5777C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405821 | |||||||
chr11:32405875 | C | T | 3 | a0001c0010t0014g0268 a0001c0010t0016g0269 a0001c0016t0016g0298 |
3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-5831G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405875 | |||||||
chr11:32405882 | T | G | 144 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(141): Show |
148 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1017-5838A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405882 | |||||||
chr11:32405937 | G | A | 1 | a0001c0005t0002g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1017-5893C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405937 | |||||||
chr11:32405966 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1017-5922C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405966 | |||||||
chr11:32406133 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1017-6089C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406133 | |||||||
chr11:32406191 | A | C | 1 | a0001c0002t0001g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1017-6147T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406191 | |||||||
chr11:32406277 | G | A | 144 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(141): Show |
148 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1017-6233C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406277 | |||||||
chr11:32406283 | C | T | 3 | a0001c0010t0014g0268 a0001c0010t0016g0269 a0001c0016t0016g0298 |
3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-6239G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406283 | |||||||
chr11:32406319 | A | T | 2 | a0001c0002t0001g0075 a0001c0006t0001g0198 |
2 | HG00408.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1017-6275T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406319 | |||||||
chr11:32406459 | G | A | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-6415C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406459 | |||||||
chr11:32406486 | A | C | 138 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(135): Show |
142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1017-6442T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406486 | |||||||
chr11:32406618 | C | T | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-6574G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406618 | |||||||
chr11:32406628 | A | AT | 137 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(134): Show |
141 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1017-6585_1017-658 others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406628 | |||||||
chr11:32406630 | A | AT | 3 | a0001c0002t0001g0042 a0001c0002t0001g0095 a0001c0004t0017g0278 |
3 | HG00558.hp1 HG02818.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1017-6587_1017-658 others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406630 | |||||||
chr11:32406630 | A | T | 182 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(179): Show |
190 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1017-6586T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406630 | |||||||
chr11:32406632 | T | A | 1 | a0001c0002t0001g0080 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1017-6588A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406632 | |||||||
chr11:32406642 | T | C | 1 | a0001c0009t0008g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1017-6598A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406642 | |||||||
chr11:32406771 | C | T | 10 | a0001c0003t0006g0218 a0001c0003t0006g0219 a0001c0003t0006g0222 others(7): Show |
11 | HG02145.hp2 HG02559.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1017-6727G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406771 | |||||||
chr11:32406816 | C | T | 2 | a0001c0005t0002g0212 a0001c0005t0002g0252 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1017-6772G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406816 | |||||||
chr11:32406956 | G | A | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-6912C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406956 | |||||||
chr11:32406999 | T | C | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-6955A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406999 | |||||||
chr11:32407170 | G | A | 2 | a0001c0005t0002g0212 a0001c0005t0002g0252 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1017-7126C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407170 | |||||||
chr11:32407238 | GAAAAACA others(1): Show |
G | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-7202_1017-719 others(12): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407238 | |||||||
chr11:32407252 | CA | C | 5 | a0001c0002t0001g0002 a0001c0002t0001g0048 a0001c0002t0001g0050 others(2): Show |
8 | NA18960.hp2 NA18961.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1017-7209delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407252 | |||||||
chr11:32407405 | CAGA | C | 7 | a0001c0003t0003g0237 a0001c0003t0003g0242 a0001c0003t0003g0250 others(4): Show |
7 | HG03017.hp2 HG03491.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017-7364_1017-736 others(7): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407405 | |||||||
chr11:32407432 | A | G | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-7388T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407432 | |||||||
chr11:32407510 | C | T | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-7466G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407510 | |||||||
chr11:32407549 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1017-7505G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407549 | |||||||
chr11:32407550 | C | T | 34 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(31): Show |
35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1017-7506G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407550 | |||||||
chr11:32407553 | C | T | 176 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(173): Show |
184 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1017-7509G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407553 | |||||||
chr11:32407558 | T | C | 3 | a0001c0010t0014g0268 a0001c0010t0016g0269 a0001c0016t0016g0298 |
3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-7514A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407558 | |||||||
chr11:32407713 | T | C | 138 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(135): Show |
142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1017-7669A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407713 | |||||||
chr11:32407715 | T | C | 3 | a0001c0010t0014g0268 a0001c0010t0016g0269 a0001c0016t0016g0298 |
3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-7671A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407715 | |||||||
chr11:32407912 | C | T | 12 | a0001c0003t0006g0218 a0001c0003t0006g0219 a0001c0003t0006g0222 others(9): Show |
13 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1017-7868G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407912 | |||||||
chr11:32407949 | G | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0202 |
2 | HG00597.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1017-7905C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407949 | |||||||
chr11:32407957 | T | C | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-7913A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407957 | |||||||
chr11:32407971 | C | T | 12 | a0001c0003t0006g0218 a0001c0003t0006g0219 a0001c0003t0006g0222 others(9): Show |
13 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1017-7927G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407971 | |||||||
chr11:32408116 | G | C | 3 | a0001c0010t0014g0268 a0001c0010t0016g0269 a0001c0016t0016g0298 |
3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-8072C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408116 | |||||||
chr11:32408120 | G | A | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-8076C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408120 | |||||||
chr11:32408121 | G | T | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-8077C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408121 | |||||||
chr11:32408127 | G | A | 2 | a0001c0002t0001g0073 a0001c0006t0001g0163 |
2 | NA18944.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1017-8083C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408127 | |||||||
chr11:32408161 | T | C | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-8117A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408161 | |||||||
chr11:32408203 | C | T | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1017-8159G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408203 | |||||||
chr11:32408213 | G | GA | 11 | a0001c0002t0001g0052 a0001c0002t0001g0066 a0001c0003t0029g0220 others(8): Show |
11 | HG01884.hp1 HG02559.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1017-8170dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408213 | |||||||
chr11:32408213 | G | GAA | 94 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(91): Show |
97 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1017-8171_1017-817 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408213 | |||||||
chr11:32408213 | G | GAAA | 33 | a0001c0001t0002g0111 a0001c0001t0002g0136 a0001c0001t0002g0148 others(30): Show |
34 | HG00642.hp1 HG00735.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1017-8172_1017-817 others(7): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408213 | |||||||
chr11:32408213 | G | GAAAA | 6 | a0001c0003t0003g0245 a0001c0003t0003g0246 a0001c0003t0003g0247 others(3): Show |
6 | HG00733.hp2 HG01261.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017-8173_1017-817 others(8): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408213 | |||||||
chr11:32408330 | T | G | 1 | a0001c0002t0007g0044 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1016+8160A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408330 | |||||||
chr11:32408356 | A | T | 2 | a0001c0005t0002g0212 a0001c0005t0002g0252 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+8134T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408356 | |||||||
chr11:32408514 | T | TA | 33 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(30): Show |
41 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1016+7975dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | |||||||
chr11:32408514 | TA | T | 8 | a0001c0002t0001g0061 a0001c0002t0001g0074 a0001c0002t0001g0092 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+7975delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | |||||||
chr11:32408514 | TAAAA | T | 16 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(13): Show |
17 | HG01496.hp1 HG02129.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1016+7972_1016+797 others(8): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | |||||||
chr11:32408514 | TAAAAA | T | 20 | a0001c0002t0004g0029 a0001c0002t0011g0026 a0001c0002t0011g0027 others(17): Show |
23 | HG01099.hp1 HG01175.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1016+7971_1016+797 others(9): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | |||||||
chr11:32408514 | TAAAAAA | T | 20 | a0001c0002t0004g0028 a0001c0003t0001g0230 a0001c0003t0001g0231 others(17): Show |
21 | HG00733.hp2 HG01109.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1016+7970_1016+797 others(10): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | |||||||
chr11:32408514 | TAAAAAAA | T | 28 | a0001c0001t0002g0173 a0001c0001t0002g0208 a0001c0002t0001g0070 others(25): Show |
29 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1016+7969_1016+797 others(11): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | |||||||
chr11:32408514 | TAAAAAAA others(1): Show |
T | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
99 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1016+7968_1016+797 others(12): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | |||||||
chr11:32408514 | TAAAAAAA others(3): Show |
T | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+7966_1016+797 others(14): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | |||||||
chr11:32408514 | TAAAAAAA others(8): Show |
T | 2 | a0001c0002t0001g0064 a0001c0006t0001g0115 |
2 | NA18955.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1016+7961_1016+797 others(19): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | |||||||
chr11:32408536 | A | G | 2 | a0001c0001t0013g0141 a0001c0001t0013g0147 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1016+7954T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408536 | |||||||
chr11:32408540 | A | G | 140 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(137): Show |
144 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1016+7950T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408540 | |||||||
chr11:32408829 | T | C | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+7661A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408829 | |||||||
chr11:32408851 | G | A | 2 | a0001c0005t0002g0212 a0001c0005t0002g0252 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+7639C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408851 | |||||||
chr11:32408939 | T | C | 138 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(135): Show |
142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1016+7551A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408939 | |||||||
chr11:32408955 | T | C | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+7535A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408955 | |||||||
chr11:32409055 | G | A | 201 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(198): Show |
211 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.1016+7435C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409055 | |||||||
chr11:32409083 | T | C | 2 | a0001c0005t0002g0212 a0001c0005t0002g0252 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+7407A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409083 | |||||||
chr11:32409109 | G | A | 3 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0015g0056 |
8 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+7381C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409109 | |||||||
chr11:32409192 | T | A | 1 | a0001c0002t0001g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1016+7298A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409192 | |||||||
chr11:32409193 | G | T | 1 | a0001c0002t0001g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1016+7297C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409193 | |||||||
chr11:32409194 | T | G | 1 | a0001c0002t0001g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1016+7296A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409194 | |||||||
chr11:32409232 | A | T | 97 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(94): Show |
100 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1016+7258T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409232 | |||||||
chr11:32409240 | C | T | 32 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(29): Show |
36 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(33): Show |
intron_variant | MODIFIER | c.1016+7250G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409240 | |||||||
chr11:32409301 | G | T | 2 | a0001c0008t0003g0284 a0001c0008t0003g0288 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1016+7189C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409301 | |||||||
chr11:32409543 | C | A | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+6947G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409543 | |||||||
chr11:32409731 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1016+6759G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409731 | |||||||
chr11:32409798 | G | A | 140 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(137): Show |
144 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1016+6692C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409798 | |||||||
chr11:32409894 | AT | A | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+6595delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409894 | |||||||
chr11:32410028 | G | A | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1016+6462C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410028 | |||||||
chr11:32410133 | G | A | 9 | a0001c0003t0006g0218 a0001c0003t0006g0219 a0001c0003t0006g0222 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1016+6357C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410133 | |||||||
chr11:32410183 | G | A | 3 | a0001c0010t0014g0268 a0001c0010t0016g0269 a0001c0016t0016g0298 |
3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1016+6307C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410183 | |||||||
chr11:32410243 | C | A | 5 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0009t0033g0305 others(2): Show |
6 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+6247G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410243 | |||||||
chr11:32410264 | A | G | 1 | a0001c0005t0005g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1016+6226T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410264 | |||||||
chr11:32410338 | C | T | 1 | a0001c0005t0005g0261 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1016+6152G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410338 | |||||||
chr11:32410399 | C | T | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1016+6091G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410399 | |||||||
chr11:32410463 | C | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0146 |
2 | NA18995.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1016+6027G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410463 | |||||||
chr11:32410477 | G | A | 138 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(135): Show |
142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1016+6013C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410477 | |||||||
chr11:32410513 | T | C | 3 | a0001c0003t0010g0018 a0001c0003t0010g0019 a0001c0003t0010g0020 |
3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1016+5977A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410513 | |||||||
chr11:32410598 | C | T | 4 | a0001c0003t0010g0018 a0001c0003t0010g0019 a0001c0003t0010g0020 others(1): Show |
4 | HG01496.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+5892G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410598 | |||||||
chr11:32410620 | T | A | 1 | a0001c0010t0008g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1016+5870A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410620 | |||||||
chr11:32410847 | G | A | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+5643C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410847 | |||||||
chr11:32411068 | T | TAC | 8 | a0001c0002t0001g0095 a0001c0002t0001g0110 a0001c0002t0011g0026 others(5): Show |
8 | HG00558.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+5420_1016+542 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(3): Show |
6 | a0001c0001t0002g0160 a0001c0001t0002g0188 a0001c0004t0009g0287 others(3): Show |
6 | HG00438.hp2 HG01891.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+5412_1016+542 others(14): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(5): Show |
13 | a0001c0001t0002g0010 a0001c0001t0002g0124 a0001c0001t0002g0127 others(10): Show |
14 | HG02074.hp2 HG03453.hp2 HG03516.hp2 others(11): Show |
intron_variant | MODIFIER | c.1016+5410_1016+542 others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(7): Show |
76 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0111 others(73): Show |
78 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1016+5408_1016+542 others(18): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(9): Show |
8 | a0001c0001t0002g0120 a0001c0001t0002g0122 a0001c0001t0002g0178 others(5): Show |
8 | HG01884.hp1 HG01934.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+5406_1016+542 others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(11): Show |
8 | a0001c0003t0032g0229 a0001c0004t0003g0017 a0001c0004t0003g0272 others(5): Show |
9 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1016+5404_1016+542 others(22): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(13): Show |
9 | a0001c0003t0024g0232 a0001c0008t0003g0284 a0001c0008t0003g0286 others(6): Show |
9 | HG00642.hp1 HG01175.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1016+5402_1016+542 others(24): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(15): Show |
5 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0025g0233 others(2): Show |
5 | HG01099.hp1 HG01169.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016+5400_1016+542 others(26): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(17): Show |
6 | a0001c0003t0003g0237 a0001c0003t0003g0247 a0001c0003t0003g0250 others(3): Show |
6 | HG03017.hp2 HG03491.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+5398_1016+542 others(28): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(19): Show |
6 | a0001c0003t0003g0243 a0001c0003t0003g0244 a0001c0003t0003g0245 others(3): Show |
6 | HG00733.hp2 HG01361.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+5396_1016+542 others(30): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(21): Show |
1 | a0001c0003t0003g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1016+5421_1016+542 others(32): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(23): Show |
1 | a0001c0003t0003g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1016+5421_1016+542 others(34): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACACA others(27): Show |
1 | a0001c0003t0003g0248 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1016+5421_1016+542 others(38): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | T | TACACAGA others(7): Show |
1 | a0001c0001t0002g0171 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1016+5421_1016+542 others(18): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411068 | TAC | T | 4 | a0001c0004t0007g0285 a0001c0010t0014g0268 a0001c0010t0016g0269 others(1): Show |
4 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1016+5420_1016+542 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | |||||||
chr11:32411351 | C | G | 2 | a0001c0002t0011g0026 a0001c0002t0011g0027 |
2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1016+5139G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411351 | |||||||
chr11:32411497 | G | T | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
99 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1016+4993C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411497 | |||||||
chr11:32411498 | T | C | 1 | a0001c0004t0017g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1016+4992A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411498 | |||||||
chr11:32411616 | C | A | 3 | a0001c0003t0003g0243 a0001c0003t0003g0244 a0001c0003t0003g0245 |
3 | HG00733.hp2 HG01361.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1016+4874G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411616 | |||||||
chr11:32411653 | C | T | 2 | a0001c0005t0002g0212 a0001c0005t0002g0252 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+4837G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411653 | |||||||
chr11:32411698 | A | G | 1 | a0001c0002t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1016+4792T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411698 | |||||||
chr11:32411775 | A | G | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1016+4715T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411775 | |||||||
chr11:32411879 | T | C | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+4611A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411879 | |||||||
chr11:32411883 | G | GA | 6 | a0001c0002t0001g0048 a0001c0003t0001g0230 a0001c0003t0001g0231 others(3): Show |
6 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+4606dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411883 | |||||||
chr11:32411901 | T | C | 34 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(31): Show |
35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1016+4589A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411901 | |||||||
chr11:32411924 | G | A | 1 | a0001c0009t0033g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1016+4566C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411924 | |||||||
chr11:32411933 | T | G | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+4557A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411933 | |||||||
chr11:32411951 | G | T | 1 | a0001c0001t0002g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1016+4539C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411951 | |||||||
chr11:32411958 | G | C | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1016+4532C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411958 | |||||||
chr11:32411973 | G | T | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+4517C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411973 | |||||||
chr11:32411983 | T | C | 1 | a0001c0002t0001g0081 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1016+4507A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411983 | |||||||
chr11:32411998 | G | C | 34 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(31): Show |
35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1016+4492C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411998 | |||||||
chr11:32412032 | G | T | 1 | a0001c0001t0002g0122 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1016+4458C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412032 | |||||||
chr11:32412326 | T | C | 138 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(135): Show |
142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1016+4164A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412326 | |||||||
chr11:32412496 | T | C | 1 | a0001c0003t0004g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1016+3994A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412496 | |||||||
chr11:32412560 | G | C | 2 | a0001c0003t0004g0236 a0001c0003t0004g0240 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1016+3930C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412560 | |||||||
chr11:32412606 | T | C | 31 | a0001c0001t0005g0008 a0001c0001t0005g0116 a0001c0001t0005g0118 others(28): Show |
35 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(32): Show |
intron_variant | MODIFIER | c.1016+3884A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412606 | |||||||
chr11:32412634 | G | A | 134 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(131): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1016+3856C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412634 | |||||||
chr11:32412711 | C | T | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+3779G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412711 | |||||||
chr11:32412717 | T | TAAAAATC others(303): Show |
2 | a0001c0001t0002g0134 a0001c0007t0002g0041 |
2 | HG03704.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1016+3772_1016+377 others(314): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | |||||||
chr11:32412717 | T | TAAAAATC others(304): Show |
87 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0111 others(84): Show |
89 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1016+3772_1016+377 others(315): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | |||||||
chr11:32412717 | T | TAAAAATC others(305): Show |
7 | a0001c0001t0002g0009 a0001c0001t0002g0114 a0001c0001t0002g0140 others(4): Show |
8 | HG01346.hp1 HG02258.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+3772_1016+377 others(316): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | |||||||
chr11:32412717 | T | TAAAAATC others(313): Show |
1 | a0001c0004t0009g0293 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1016+3772_1016+377 others(324): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | |||||||
chr11:32412717 | T | TAAAAATC others(315): Show |
2 | a0001c0004t0009g0287 a0001c0004t0009g0295 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1016+3772_1016+377 others(326): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | |||||||
chr11:32412717 | T | TAAAAATC others(307): Show |
1 | a0001c0005t0002g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1016+3772_1016+377 others(318): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | |||||||
chr11:32412720 | A | AAATCTAA others(302): Show |
1 | a0001c0003t0032g0229 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1016+3769_1016+377 others(313): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412720 | |||||||
chr11:32412720 | A | AAATCTAA others(303): Show |
4 | a0001c0003t0003g0237 a0001c0003t0003g0242 a0001c0003t0003g0246 others(1): Show |
4 | HG01261.hp2 HG03017.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1016+3769_1016+377 others(314): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412720 | |||||||
chr11:32412720 | A | AAATCTAA others(302): Show |
29 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(26): Show |
30 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1016+3769_1016+377 others(313): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412720 | |||||||
chr11:32412768 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1016+3722C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412768 | |||||||
chr11:32413015 | G | T | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1016+3475C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413015 | |||||||
chr11:32413028 | A | T | 2 | a0001c0005t0002g0212 a0001c0005t0002g0252 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+3462T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413028 | |||||||
chr11:32413059 | T | A | 4 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0010t0008g0217 others(1): Show |
5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1016+3431A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413059 | |||||||
chr11:32413080 | G | A | 128 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(125): Show |
132 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1016+3410C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413080 | |||||||
chr11:32413355 | G | A | 34 | a0001c0002t0003g0060 a0001c0002t0003g0069 a0001c0003t0003g0213 others(31): Show |
35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1016+3135C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413355 | |||||||
chr11:32413446 | C | T | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+3044G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413446 | |||||||
chr11:32413501 | AT | A | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+2988delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413501 | |||||||
chr11:32413530 | A | G | 1 | a0001c0002t0001g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1016+2960T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413530 | |||||||
chr11:32413637 | A | G | 1 | a0001c0001t0002g0159 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1016+2853T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413637 | |||||||
chr11:32413643 | A | G | 4 | a0001c0002t0011g0026 a0001c0004t0009g0287 a0001c0004t0009g0293 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1016+2847T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413643 | |||||||
chr11:32413939 | C | T | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1016+2551G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413939 | |||||||
chr11:32413978 | G | A | 1 | a0001c0005t0002g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1016+2512C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413978 | |||||||
chr11:32413983 | G | A | 30 | a0001c0001t0002g0138 a0001c0001t0005g0008 a0001c0001t0005g0116 others(27): Show |
34 | HG02129.hp2 HG02257.hp2 HG02622.hp2 others(31): Show |
intron_variant | MODIFIER | c.1016+2507C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413983 | |||||||
chr11:32413998 | A | G | 4 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+2492T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413998 | |||||||
chr11:32414011 | T | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+2479A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414011 | |||||||
chr11:32414016 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1016+2474G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414016 | |||||||
chr11:32414026 | G | A | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+2464C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414026 | |||||||
chr11:32414078 | T | C | 1 | a0001c0012t0014g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1016+2412A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414078 | |||||||
chr11:32414084 | C | T | 4 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0010t0008g0217 others(1): Show |
5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1016+2406G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414084 | |||||||
chr11:32414085 | G | A | 15 | a0001c0001t0002g0138 a0001c0001t0005g0008 a0001c0001t0005g0116 others(12): Show |
16 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.1016+2405C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414085 | |||||||
chr11:32414129 | T | C | 1 | a0001c0006t0001g0197 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1016+2361A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414129 | |||||||
chr11:32414192 | C | G | 3 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0002g0159 |
3 | HG02074.hp2 NA18952.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1016+2298G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414192 | |||||||
chr11:32414307 | C | T | 2 | a0001c0002t0001g0090 a0001c0002t0001g0096 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1016+2183G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414307 | |||||||
chr11:32414325 | T | C | 1 | a0001c0001t0019g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1016+2165A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414325 | |||||||
chr11:32414454 | T | C | 5 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0009t0033g0305 others(2): Show |
6 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+2036A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414454 | |||||||
chr11:32414519 | C | T | 2 | a0001c0003t0006g0218 a0001c0003t0006g0222 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1016+1971G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414519 | |||||||
chr11:32414599 | G | A | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+1891C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414599 | |||||||
chr11:32414602 | G | A | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+1888C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414602 | |||||||
chr11:32414648 | G | A | 2 | a0001c0001t0002g0114 a0001c0005t0002g0221 |
2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1016+1842C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414648 | |||||||
chr11:32414868 | A | G | 165 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(162): Show |
173 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.1016+1622T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414868 | |||||||
chr11:32414872 | C | CA | 18 | a0001c0001t0002g0168 a0001c0001t0019g0021 a0001c0002t0001g0052 others(15): Show |
19 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1016+1617dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414872 | |||||||
chr11:32414872 | CA | C | 11 | a0001c0001t0002g0191 a0001c0002t0001g0063 a0001c0002t0001g0097 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.1016+1617delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414872 | |||||||
chr11:32414873 | A | C | 6 | a0001c0003t0003g0243 a0001c0003t0003g0244 a0001c0003t0003g0245 others(3): Show |
6 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+1617T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414873 | |||||||
chr11:32415345 | AC | A | 5 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0009t0033g0305 others(2): Show |
6 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+1144delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415345 | |||||||
chr11:32415386 | C | T | 1 | a0001c0003t0006g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1016+1104G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415386 | |||||||
chr11:32415417 | G | C | 1 | a0001c0004t0004g0274 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1016+1073C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415417 | |||||||
chr11:32415439 | G | A | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+1051C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415439 | |||||||
chr11:32415555 | G | A | 2 | a0001c0003t0003g0213 a0001c0003t0003g0214 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1016+935C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415555 | |||||||
chr11:32415572 | C | T | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+918G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415572 | |||||||
chr11:32415643 | G | A | 32 | a0001c0003t0003g0213 a0001c0003t0003g0214 a0001c0003t0003g0237 others(29): Show |
33 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1016+847C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415643 | |||||||
chr11:32415663 | T | C | 168 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(165): Show |
176 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.1016+827A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415663 | |||||||
chr11:32415764 | A | T | 6 | a0001c0003t0003g0243 a0001c0003t0003g0244 a0001c0003t0003g0245 others(3): Show |
6 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+726T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415764 | |||||||
chr11:32415981 | T | G | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+509A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415981 | |||||||
chr11:32416079 | G | C | 1 | a0001c0002t0001g0084 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1016+411C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416079 | |||||||
chr11:32416086 | A | G | 5 | a0001c0003t0004g0014 a0001c0003t0004g0236 a0001c0003t0004g0238 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+404T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416086 | |||||||
chr11:32416131 | G | C | 166 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(163): Show |
174 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1016+359C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416131 | |||||||
chr11:32416153 | T | C | 294 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(291): Show |
317 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.1016+337A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416153 | |||||||
chr11:32416270 | T | A | 1 | a0001c0002t0001g0104 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1016+220A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416270 | |||||||
chr11:32416295 | A | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+195T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416295 | |||||||
chr11:32416326 | T | A | 27 | a0001c0001t0002g0186 a0001c0002t0004g0028 a0001c0002t0004g0029 others(24): Show |
30 | HG02129.hp2 HG02257.hp2 HG02622.hp2 others(27): Show |
intron_variant | MODIFIER | c.1016+164A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416326 | |||||||
chr11:32416327 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1016+163C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416327 | |||||||
chr11:32416356 | G | A | 32 | a0001c0003t0003g0213 a0001c0003t0003g0214 a0001c0003t0003g0237 others(29): Show |
33 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1016+134C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416356 | |||||||
chr11:32416368 | T | G | 162 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(159): Show |
170 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.1016+122A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416368 | |||||||
chr11:32416409 | G | A | 3 | a0001c0003t0010g0018 a0001c0003t0010g0019 a0001c0003t0010g0020 |
3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1016+81C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416409 | |||||||
chr11:32416564 | A | G | 1 | a0001c0005t0002g0221 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.966-24T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416564 | |||||||
chr11:32416708 | G | A | 1 | a0001c0005t0005g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.966-168C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416708 | |||||||
chr11:32416784 | T | G | 1 | a0001c0004t0004g0297 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.966-244A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416784 | |||||||
chr11:32416931 | T | C | 169 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(166): Show |
177 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.966-391A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416931 | |||||||
chr11:32416973 | A | C | 2 | a0001c0005t0002g0212 a0001c0005t0002g0252 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.966-433T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416973 | |||||||
chr11:32417032 | T | C | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.966-492A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417032 | |||||||
chr11:32417138 | C | T | 100 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(97): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.965+439G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417138 | |||||||
chr11:32417148 | T | C | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.965+429A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417148 | |||||||
chr11:32417153 | G | A | 167 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(164): Show |
175 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.965+424C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417153 | |||||||
chr11:32417207 | C | T | 199 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(196): Show |
209 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.965+370G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417207 | |||||||
chr11:32417208 | G | C | 1 | a0001c0004t0001g0015 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.965+369C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417208 | |||||||
chr11:32417242 | T | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+335A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417242 | |||||||
chr11:32417322 | A | G | 1 | a0001c0002t0001g0007 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.965+255T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417322 | |||||||
chr11:32417447 | T | G | 1 | a0001c0010t0021g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.965+130A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417447 | |||||||
chr11:32417455 | T | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+122A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417455 | |||||||
chr11:32417492 | T | C | 167 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(164): Show |
175 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.965+85A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417492 | |||||||
chr11:32417752 | C | T | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-98G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32417752 | |||||||
chr11:32417946 | G | A | 2 | a0001c0002t0001g0090 a0001c0002t0001g0096 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.888-292C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32417946 | |||||||
chr11:32418242 | A | ATG | 6 | a0001c0007t0002g0033 a0001c0007t0028g0034 a0001c0010t0014g0270 others(3): Show |
6 | HG01243.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.888-589_888-588ins others(2): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418242 | |||||||
chr11:32418243 | T | TG | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(119): Show |
126 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.888-590_888-589ins others(1): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418243 | |||||||
chr11:32418244 | T | A | 5 | a0001c0007t0028g0034 a0001c0010t0014g0270 a0001c0010t0021g0215 others(2): Show |
5 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.888-590A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418244 | |||||||
chr11:32418244 | T | G | 39 | a0001c0001t0002g0204 a0001c0002t0004g0028 a0001c0002t0004g0029 others(36): Show |
43 | HG00642.hp1 HG00735.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.888-590A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418244 | |||||||
chr11:32418244 | T | TA | 103 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(100): Show |
117 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.888-591dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418244 | |||||||
chr11:32418245 | A | T | 39 | a0001c0001t0002g0204 a0001c0002t0004g0028 a0001c0002t0004g0029 others(36): Show |
43 | HG00642.hp1 HG00735.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.888-591T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418245 | |||||||
chr11:32418253 | A | G | 3 | a0001c0002t0011g0026 a0001c0002t0011g0027 a0001c0002t0011g0030 |
3 | HG02572.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.888-599T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418253 | |||||||
chr11:32418278 | C | T | 167 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(164): Show |
175 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.888-624G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418278 | |||||||
chr11:32418334 | G | A | 32 | a0001c0003t0003g0213 a0001c0003t0003g0214 a0001c0003t0003g0237 others(29): Show |
33 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.888-680C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418334 | |||||||
chr11:32418492 | A | C | 46 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0003t0002g0227 others(43): Show |
50 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.888-838T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418492 | |||||||
chr11:32418581 | A | T | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
100 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.888-927T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418581 | |||||||
chr11:32418692 | C | A | 1 | a0001c0002t0001g0068 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.888-1038G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418692 | |||||||
chr11:32418727 | A | G | 1 | a0001c0005t0005g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.888-1073T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418727 | |||||||
chr11:32418801 | C | T | 1 | a0001c0002t0001g0006 | 2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.888-1147G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418801 | |||||||
chr11:32418803 | G | A | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.888-1149C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418803 | |||||||
chr11:32418810 | G | A | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-1156C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418810 | |||||||
chr11:32418830 | C | A | 1 | a0001c0007t0002g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.888-1176G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418830 | |||||||
chr11:32419095 | T | C | 7 | a0001c0003t0003g0237 a0001c0003t0003g0242 a0001c0003t0003g0250 others(4): Show |
7 | HG03017.hp2 HG03491.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.888-1441A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419095 | |||||||
chr11:32419109 | C | T | 3 | a0001c0003t0010g0018 a0001c0003t0010g0019 a0001c0003t0010g0020 |
3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.888-1455G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419109 | |||||||
chr11:32419195 | T | G | 1 | a0001c0003t0003g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.888-1541A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419195 | |||||||
chr11:32419479 | A | T | 1 | a0001c0004t0003g0292 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.888-1825T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419479 | |||||||
chr11:32419565 | C | T | 58 | a0001c0001t0002g0186 a0001c0002t0004g0028 a0001c0002t0004g0029 others(55): Show |
62 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.888-1911G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419565 | |||||||
chr11:32419577 | C | A | 1 | a0001c0002t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.888-1923G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419577 | |||||||
chr11:32419710 | G | A | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-2056C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419710 | |||||||
chr11:32419743 | G | C | 3 | a0001c0001t0002g0193 a0001c0001t0002g0202 a0001c0005t0002g0241 |
3 | HG00597.hp2 NA18940.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.888-2089C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419743 | |||||||
chr11:32419825 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.888-2171G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419825 | |||||||
chr11:32419831 | C | T | 201 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(198): Show |
211 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.888-2177G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419831 | |||||||
chr11:32420166 | G | A | 3 | a0001c0010t0014g0268 a0001c0010t0016g0269 a0001c0016t0016g0298 |
3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.888-2512C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420166 | |||||||
chr11:32420364 | T | C | 14 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0003t0002g0227 others(11): Show |
17 | HG02257.hp2 HG02622.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.888-2710A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420364 | |||||||
chr11:32420453 | C | T | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-2799G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420453 | |||||||
chr11:32420456 | T | C | 1 | a0001c0005t0022g0265 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.888-2802A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420456 | |||||||
chr11:32420504 | A | G | 13 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0003t0004g0012 others(10): Show |
16 | HG02257.hp2 HG02622.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.888-2850T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420504 | |||||||
chr11:32420551 | G | C | 1 | a0001c0009t0033g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.888-2897C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420551 | |||||||
chr11:32420555 | C | T | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-2901G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420555 | |||||||
chr11:32420588 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.888-2934T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420588 | |||||||
chr11:32420618 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.888-2964G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420618 | |||||||
chr11:32420641 | A | G | 2 | a0001c0006t0001g0145 a0001c0006t0001g0153 |
2 | NA18995.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.888-2987T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420641 | |||||||
chr11:32420729 | A | G | 166 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(163): Show |
174 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.888-3075T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420729 | |||||||
chr11:32420922 | G | T | 6 | a0001c0003t0003g0243 a0001c0003t0003g0244 a0001c0003t0003g0245 others(3): Show |
6 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.888-3268C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420922 | |||||||
chr11:32420992 | A | C | 1 | a0001c0001t0005g0158 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.888-3338T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420992 | |||||||
chr11:32420994 | A | C | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.888-3340T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420994 | |||||||
chr11:32421042 | C | T | 1 | a0001c0003t0032g0229 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.888-3388G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421042 | |||||||
chr11:32421090 | A | G | 168 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(165): Show |
176 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.888-3436T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421090 | |||||||
chr11:32421109 | C | T | 3 | a0001c0003t0001g0263 a0001c0005t0005g0261 a0001c0005t0022g0265 |
3 | NA18950.hp2 NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.888-3455G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421109 | |||||||
chr11:32421187 | T | C | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-3533A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421187 | |||||||
chr11:32421301 | G | C | 4 | a0001c0010t0014g0270 a0001c0010t0021g0215 a0001c0012t0014g0210 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-3647C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421301 | |||||||
chr11:32421360 | C | A | 1 | a0001c0004t0003g0302 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.888-3706G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421360 | |||||||
chr11:32421498 | T | A | 4 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0010t0008g0217 others(1): Show |
5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.888-3844A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421498 | |||||||
chr11:32421775 | G | C | 1 | a0001c0006t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.888-4121C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421775 | |||||||
chr11:32422153 | G | A | 2 | a0001c0003t0024g0232 a0001c0003t0025g0233 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.888-4499C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422153 | |||||||
chr11:32422244 | C | T | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.888-4590G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422244 | |||||||
chr11:32422474 | A | G | 176 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(173): Show |
186 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.888-4820T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422474 | |||||||
chr11:32422489 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.888-4835C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422489 | |||||||
chr11:32422543 | G | T | 1 | a0001c0009t0008g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.888-4889C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422543 | |||||||
chr11:32422547 | A | G | 3 | a0001c0003t0010g0018 a0001c0003t0010g0019 a0001c0003t0010g0020 |
3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.888-4893T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422547 | |||||||
chr11:32422600 | C | T | 2 | a0001c0002t0003g0060 a0001c0002t0003g0069 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.888-4946G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422600 | |||||||
chr11:32422601 | G | A | 175 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(172): Show |
185 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.888-4947C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422601 | |||||||
chr11:32422656 | G | A | 3 | a0001c0003t0001g0253 a0001c0005t0002g0212 a0001c0005t0002g0252 |
3 | HG01884.hp1 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.888-5002C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422656 | |||||||
chr11:32422698 | G | T | 2 | a0001c0010t0014g0268 a0001c0010t0016g0269 |
2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.888-5044C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422698 | |||||||
chr11:32422757 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.888-5103A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422757 | |||||||
chr11:32422811 | C | G | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.887+5145G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422811 | |||||||
chr11:32422829 | T | C | 176 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(173): Show |
186 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.887+5127A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422829 | |||||||
chr11:32422861 | G | A | 9 | a0001c0006t0001g0211 a0001c0009t0008g0004 a0001c0009t0008g0035 others(6): Show |
10 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.887+5095C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422861 | |||||||
chr11:32422953 | C | T | 7 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0055 others(4): Show |
12 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+5003G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422953 | |||||||
chr11:32423134 | C | A | 1 | a0001c0010t0008g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.887+4822G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423134 | |||||||
chr11:32423219 | G | A | 33 | a0001c0004t0001g0015 a0001c0004t0001g0279 a0001c0004t0001g0281 others(30): Show |
35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+4737C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423219 | |||||||
chr11:32423240 | C | T | 3 | a0001c0004t0009g0287 a0001c0004t0009g0293 a0001c0004t0009g0295 |
3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.887+4716G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423240 | |||||||
chr11:32423262 | G | A | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+4694C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423262 | |||||||
chr11:32423436 | G | C | 4 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0010t0008g0217 others(1): Show |
5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+4520C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423436 | |||||||
chr11:32423649 | T | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+4307A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423649 | |||||||
chr11:32423679 | T | C | 1 | a0001c0007t0002g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.887+4277A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423679 | |||||||
chr11:32423701 | C | A | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.887+4255G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423701 | |||||||
chr11:32423860 | T | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+4096A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423860 | |||||||
chr11:32424066 | G | A | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+3890C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424066 | |||||||
chr11:32424086 | C | T | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+3870G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424086 | |||||||
chr11:32424160 | C | CA | 7 | a0001c0003t0006g0226 a0001c0006t0001g0211 a0001c0010t0014g0270 others(4): Show |
7 | HG02257.hp1 HG02280.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+3795dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | |||||||
chr11:32424160 | C | CAA | 18 | a0001c0001t0002g0128 a0001c0001t0002g0133 a0001c0001t0002g0157 others(15): Show |
19 | HG00438.hp1 HG00639.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.887+3794_887+3795d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | |||||||
chr11:32424160 | C | CAAA | 116 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(113): Show |
124 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.887+3793_887+3795d others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | |||||||
chr11:32424160 | C | CAAAA | 39 | a0001c0001t0002g0121 a0001c0001t0002g0136 a0001c0001t0002g0137 others(36): Show |
40 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.887+3792_887+3795d others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | |||||||
chr11:32424160 | CA | C | 43 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(40): Show |
54 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.887+3795delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | |||||||
chr11:32424160 | CAA | C | 7 | a0001c0002t0001g0108 a0001c0003t0001g0230 a0001c0003t0001g0231 others(4): Show |
7 | HG01099.hp1 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+3794_887+3795d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | |||||||
chr11:32424160 | CAAA | C | 17 | a0001c0003t0001g0256 a0001c0003t0001g0263 a0001c0005t0002g0252 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.887+3793_887+3795d others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | |||||||
chr11:32424165 | A | T | 6 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.887+3791T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424165 | |||||||
chr11:32424187 | C | G | 1 | a0001c0003t0001g0267 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.887+3769G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424187 | |||||||
chr11:32424296 | T | C | 1 | a0001c0005t0002g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.887+3660A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424296 | |||||||
chr11:32424312 | C | T | 3 | a0001c0004t0006g0016 a0001c0004t0006g0290 a0001c0010t0006g0216 |
4 | HG02451.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+3644G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424312 | |||||||
chr11:32424334 | A | T | 1 | a0001c0001t0002g0187 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.887+3622T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424334 | |||||||
chr11:32424462 | C | G | 1 | a0001c0012t0023g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.887+3494G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424462 | |||||||
chr11:32424484 | T | G | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+3472A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424484 | |||||||
chr11:32424527 | G | A | 33 | a0001c0004t0001g0015 a0001c0004t0001g0279 a0001c0004t0001g0281 others(30): Show |
35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+3429C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424527 | |||||||
chr11:32424542 | T | C | 5 | a0001c0006t0001g0211 a0001c0010t0014g0270 a0001c0010t0021g0215 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+3414A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424542 | |||||||
chr11:32424589 | G | C | 78 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(75): Show |
83 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.887+3367C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424589 | |||||||
chr11:32424594 | T | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+3362A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424594 | |||||||
chr11:32424613 | G | A | 33 | a0001c0004t0001g0015 a0001c0004t0001g0279 a0001c0004t0001g0281 others(30): Show |
35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+3343C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424613 | |||||||
chr11:32424790 | G | A | 152 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(149): Show |
160 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.887+3166C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424790 | |||||||
chr11:32424868 | G | A | 5 | a0001c0001t0002g0149 a0001c0001t0002g0156 a0001c0001t0002g0166 others(2): Show |
5 | HG02698.hp1 HG02735.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+3088C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424868 | |||||||
chr11:32424938 | G | C | 11 | a0001c0003t0002g0227 a0001c0003t0004g0012 a0001c0003t0004g0013 others(8): Show |
14 | HG02257.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.887+3018C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424938 | |||||||
chr11:32424998 | T | C | 3 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0014t0008g0036 |
4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+2958A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424998 | |||||||
chr11:32425155 | C | A | 72 | a0001c0002t0001g0085 a0001c0002t0004g0028 a0001c0002t0004g0029 others(69): Show |
77 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.887+2801G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425155 | |||||||
chr11:32425155 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.887+2801G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425155 | |||||||
chr11:32425180 | GA | G | 107 | a0001c0001t0002g0156 a0001c0001t0012g0195 a0001c0002t0001g0001 others(104): Show |
120 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.887+2775delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425180 | |||||||
chr11:32425180 | GAA | G | 60 | a0001c0002t0001g0090 a0001c0002t0003g0060 a0001c0002t0004g0028 others(57): Show |
62 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.887+2774_887+2775d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425180 | |||||||
chr11:32425297 | G | T | 19 | a0001c0003t0003g0213 a0001c0003t0003g0214 a0001c0003t0006g0218 others(16): Show |
20 | HG01496.hp1 HG02145.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.887+2659C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425297 | |||||||
chr11:32425328 | GA | G | 67 | a0001c0002t0001g0099 a0001c0002t0011g0030 a0001c0003t0001g0253 others(64): Show |
72 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.887+2627delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425328 | |||||||
chr11:32425439 | C | A | 24 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(21): Show |
25 | HG01243.hp1 HG02129.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.887+2517G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425439 | |||||||
chr11:32425465 | A | G | 33 | a0001c0004t0001g0015 a0001c0004t0001g0279 a0001c0004t0001g0281 others(30): Show |
35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+2491T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425465 | |||||||
chr11:32425497 | G | A | 1 | a0001c0010t0016g0269 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.887+2459C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425497 | |||||||
chr11:32425505 | A | G | 4 | a0001c0004t0003g0017 a0001c0004t0003g0272 a0001c0004t0003g0299 others(1): Show |
5 | HG00735.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.887+2451T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425505 | |||||||
chr11:32425590 | A | C | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+2366T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425590 | |||||||
chr11:32425729 | A | G | 24 | a0001c0003t0002g0227 a0001c0003t0003g0237 a0001c0003t0003g0242 others(21): Show |
27 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.887+2227T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425729 | |||||||
chr11:32425801 | C | G | 221 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(218): Show |
232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.887+2155G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425801 | |||||||
chr11:32426055 | T | A | 2 | a0001c0004t0004g0273 a0001c0004t0004g0274 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.887+1901A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426055 | |||||||
chr11:32426169 | A | T | 1 | a0001c0002t0001g0073 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.887+1787T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426169 | |||||||
chr11:32426234 | G | A | 4 | a0001c0003t0001g0267 a0001c0010t0014g0268 a0001c0010t0014g0270 others(1): Show |
4 | HG01109.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+1722C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426234 | |||||||
chr11:32426296 | G | C | 1 | a0001c0007t0002g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.887+1660C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426296 | |||||||
chr11:32426318 | G | T | 67 | a0001c0003t0001g0253 a0001c0003t0001g0267 a0001c0003t0002g0227 others(64): Show |
72 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.887+1638C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426318 | |||||||
chr11:32426659 | A | G | 24 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(21): Show |
25 | HG01243.hp1 HG02129.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.887+1297T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426659 | |||||||
chr11:32426660 | A | ATT | 34 | a0001c0004t0001g0015 a0001c0004t0001g0279 a0001c0004t0001g0281 others(31): Show |
36 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.887+1295_887+1296i others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426660 | |||||||
chr11:32426672 | G | T | 21 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(18): Show |
21 | HG01243.hp1 HG02129.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.887+1284C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426672 | |||||||
chr11:32426693 | G | A | 68 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(65): Show |
73 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.887+1263C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426693 | |||||||
chr11:32426693 | G | GA | 24 | a0001c0001t0002g0112 a0001c0002t0001g0088 a0001c0002t0004g0028 others(21): Show |
24 | HG01243.hp1 HG02129.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.887+1262dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426693 | |||||||
chr11:32426709 | T | C | 218 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(215): Show |
229 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(226): Show |
intron_variant | MODIFIER | c.887+1247A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426709 | |||||||
chr11:32426754 | C | T | 1 | a0001c0004t0020g0301 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.887+1202G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426754 | |||||||
chr11:32426773 | C | A | 3 | a0001c0003t0001g0263 a0001c0005t0002g0262 a0001c0005t0022g0265 |
3 | NA18942.hp1 NA18950.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.887+1183G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426773 | |||||||
chr11:32426808 | C | T | 1 | a0001c0003t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.887+1148G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426808 | |||||||
chr11:32427023 | A | C | 221 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(218): Show |
232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.887+933T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427023 | |||||||
chr11:32427272 | G | T | 1 | a0001c0001t0002g0143 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.887+684C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427272 | |||||||
chr11:32427275 | G | A | 1 | a0001c0010t0014g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.887+681C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427275 | |||||||
chr11:32427283 | A | G | 1 | a0001c0003t0001g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.887+673T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427283 | |||||||
chr11:32427349 | C | G | 221 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(218): Show |
232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.887+607G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427349 | |||||||
chr11:32427413 | G | A | 1 | a0001c0001t0002g0193 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.887+543C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427413 | |||||||
chr11:32427552 | G | A | 4 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0024g0232 others(1): Show |
4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+404C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427552 | |||||||
chr11:32427727 | C | T | 1 | a0001c0007t0002g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.887+229G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427727 | |||||||
chr11:32427728 | G | C | 90 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(87): Show |
96 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.887+228C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427728 | |||||||
chr11:32427871 | C | G | 131 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(128): Show |
136 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.887+85G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427871 | |||||||
chr11:32427874 | C | A | 131 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(128): Show |
136 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.887+82G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427874 | |||||||
chr11:32427940 | C | T | 86 | a0001c0003t0001g0253 a0001c0003t0001g0267 a0001c0003t0002g0227 others(83): Show |
92 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.887+16G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427940 | |||||||
chr11:32428078 | C | A | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.785-20G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428078 | |||||||
chr11:32428115 | G | A | 131 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(128): Show |
136 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.785-57C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428115 | |||||||
chr11:32428218 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.785-160T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428218 | |||||||
chr11:32428230 | T | G | 2 | a0001c0004t0006g0016 a0001c0004t0006g0290 |
3 | HG02886.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.785-172A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428230 | |||||||
chr11:32428253 | G | T | 71 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(68): Show |
76 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.785-195C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428253 | |||||||
chr11:32428329 | G | A | 1 | a0001c0006t0001g0163 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.784+168C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428329 | |||||||
chr11:32428330 | G | A | 1 | a0001c0007t0002g0106 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.784+167C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428330 | |||||||
chr11:32428695 | G | A | 1 | a0001c0002t0001g0042 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.662-76C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428695 | |||||||
chr11:32428698 | C | CG | 80 | a0001c0001t0002g0114 a0001c0001t0002g0199 a0001c0003t0001g0253 others(77): Show |
86 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.662-80dupC | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428698 | |||||||
chr11:32428698 | CG | C | 10 | a0001c0002t0001g0005 a0001c0002t0001g0037 a0001c0002t0001g0039 others(7): Show |
11 | HG00408.hp1 HG00438.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.662-80delC | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428698 | |||||||
chr11:32428703 | G | A | 1 | a0001c0009t0033g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.662-84C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428703 | |||||||
chr11:32428704 | G | T | 2 | a0001c0007t0001g0054 a0001c0007t0001g0072 |
2 | HG01175.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.662-85C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428704 | |||||||
chr11:32428830 | C | G | 3 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0014t0008g0036 |
4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-211G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428830 | |||||||
chr11:32428865 | A | G | 1 | a0001c0016t0016g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.662-246T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428865 | |||||||
chr11:32429109 | T | C | 3 | a0001c0003t0010g0018 a0001c0003t0010g0019 a0001c0003t0010g0020 |
3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.662-490A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429109 | |||||||
chr11:32429119 | G | A | 5 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(2): Show |
5 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-500C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429119 | |||||||
chr11:32429187 | T | A | 3 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0014t0008g0036 |
4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-568A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429187 | |||||||
chr11:32429260 | C | A | 35 | a0001c0004t0001g0015 a0001c0004t0001g0279 a0001c0004t0001g0281 others(32): Show |
37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.662-641G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429260 | |||||||
chr11:32429279 | C | T | 70 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(67): Show |
75 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.662-660G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429279 | |||||||
chr11:32429293 | C | T | 1 | a0001c0004t0020g0301 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.662-674G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429293 | |||||||
chr11:32429304 | G | A | 4 | a0001c0003t0002g0227 a0001c0003t0004g0012 a0001c0003t0004g0013 others(1): Show |
6 | HG02647.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.662-685C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429304 | |||||||
chr11:32429330 | G | C | 1 | a0001c0007t0028g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.662-711C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429330 | |||||||
chr11:32429344 | A | G | 221 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(218): Show |
232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.662-725T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429344 | |||||||
chr11:32429457 | A | G | 221 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(218): Show |
232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.662-838T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429457 | |||||||
chr11:32429462 | T | TC | 21 | a0001c0001t0002g0132 a0001c0001t0002g0140 a0001c0001t0002g0186 others(18): Show |
22 | HG00558.hp1 HG00642.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.662-844dupG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429462 | |||||||
chr11:32429462 | TC | T | 125 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0111 others(122): Show |
128 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.662-844delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429462 | |||||||
chr11:32429462 | TCC | T | 51 | a0001c0001t0002g0124 a0001c0001t0002g0128 a0001c0001t0002g0142 others(48): Show |
56 | HG01070.hp2 HG01243.hp1 HG02129.hp2 others(53): Show |
intron_variant | MODIFIER | c.662-845_662-844del others(2): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429462 | |||||||
chr11:32429462 | TCCC | T | 23 | a0001c0002t0001g0005 a0001c0002t0001g0037 a0001c0002t0001g0038 others(20): Show |
24 | HG00408.hp1 HG00438.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.662-846_662-844del others(3): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429462 | |||||||
chr11:32429472 | C | G | 3 | a0001c0001t0002g0117 a0001c0001t0005g0008 a0001c0001t0005g0118 |
4 | HG02015.hp1 NA18973.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-853G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429472 | |||||||
chr11:32429547 | T | G | 89 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(86): Show |
95 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.662-928A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429547 | |||||||
chr11:32429553 | T | A | 221 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(218): Show |
232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.662-934A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429553 | |||||||
chr11:32429558 | C | T | 5 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(2): Show |
5 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-939G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429558 | |||||||
chr11:32429608 | C | T | 1 | a0001c0009t0033g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.662-989G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429608 | |||||||
chr11:32429709 | A | G | 1 | a0001c0005t0005g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.662-1090T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429709 | |||||||
chr11:32429796 | C | T | 1 | a0001c0002t0001g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.662-1177G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429796 | |||||||
chr11:32429978 | G | GA | 12 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(9): Show |
13 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-1360dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429978 | |||||||
chr11:32429978 | G | GAAA | 102 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(99): Show |
106 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.662-1362_662-1360d others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429978 | |||||||
chr11:32429986 | A | AG | 102 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(99): Show |
108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.662-1368_662-1367i others(3): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429986 | |||||||
chr11:32429998 | G | GA | 75 | a0001c0001t0002g0164 a0001c0001t0019g0021 a0001c0003t0002g0227 others(72): Show |
81 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.662-1380dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429998 | |||||||
chr11:32429998 | GA | G | 7 | a0001c0001t0002g0178 a0001c0002t0001g0097 a0001c0009t0008g0004 others(4): Show |
8 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.662-1380delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429998 | |||||||
chr11:32430004 | A | G | 2 | a0001c0010t0014g0268 a0001c0010t0016g0269 |
2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.662-1385T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430004 | |||||||
chr11:32430005 | A | C | 1 | a0001c0009t0033g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.662-1386T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430005 | |||||||
chr11:32430293 | A | G | 1 | a0001c0002t0001g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.662-1674T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430293 | |||||||
chr11:32430374 | T | G | 221 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(218): Show |
232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.662-1755A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430374 | |||||||
chr11:32430375 | G | C | 102 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(99): Show |
108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.662-1756C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430375 | |||||||
chr11:32430404 | A | C | 119 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(116): Show |
124 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.662-1785T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430404 | |||||||
chr11:32430432 | C | CAGAGAGA others(19): Show |
1 | a0001c0006t0001g0198 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(28): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(27): Show |
1 | a0001c0001t0002g0202 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(36): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(29): Show |
1 | a0001c0001t0002g0201 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(38): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(16): Show |
1 | a0001c0001t0002g0165 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(25): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(18): Show |
1 | a0001c0001t0002g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(27): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(30): Show |
1 | a0001c0006t0001g0211 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(39): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(17): Show |
12 | a0001c0001t0002g0009 a0001c0001t0002g0117 a0001c0001t0002g0155 others(9): Show |
13 | HG00639.hp1 HG02015.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(26): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(19): Show |
14 | a0001c0001t0002g0119 a0001c0001t0002g0121 a0001c0001t0002g0166 others(11): Show |
14 | HG00099.hp1 HG01346.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(28): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(21): Show |
11 | a0001c0001t0002g0011 a0001c0001t0002g0178 a0001c0001t0002g0179 others(8): Show |
12 | HG01071.hp2 HG01106.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(30): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(23): Show |
10 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0001t0002g0189 others(7): Show |
10 | HG00438.hp2 HG00642.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(32): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(25): Show |
4 | a0001c0001t0002g0120 a0001c0001t0002g0196 a0001c0001t0012g0195 others(1): Show |
4 | HG01361.hp2 NA18947.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(34): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(29): Show |
1 | a0001c0001t0012g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(38): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(18): Show |
1 | a0001c0001t0019g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(27): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(22): Show |
1 | a0001c0006t0009g0177 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(31): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430432 | C | CAGAGAGA others(28): Show |
1 | a0001c0001t0002g0199 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(37): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | |||||||
chr11:32430433 | A | AGAGAGAG others(14): Show |
1 | a0001c0001t0002g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.662-1815_662-1814i others(23): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430433 | |||||||
chr11:32430433 | A | AGAGAGAG others(15): Show |
17 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0001t0002g0144 others(14): Show |
17 | HG01975.hp1 HG02071.hp1 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.662-1815_662-1814i others(24): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430433 | |||||||
chr11:32430435 | A | AGAGAGAG others(13): Show |
13 | a0001c0001t0002g0010 a0001c0001t0002g0133 a0001c0001t0002g0134 others(10): Show |
15 | HG00733.hp1 HG02896.hp2 HG03669.hp1 others(12): Show |
intron_variant | MODIFIER | c.662-1817_662-1816i others(22): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430435 | |||||||
chr11:32430437 | A | AGAGAGAG others(10): Show |
1 | a0001c0001t0002g0132 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.662-1819_662-1818i others(19): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430437 | |||||||
chr11:32430437 | A | AGAGAGAG others(11): Show |
3 | a0001c0001t0002g0114 a0001c0001t0002g0131 a0001c0009t0008g0031 |
3 | HG00558.hp2 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.662-1819_662-1818i others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430437 | |||||||
chr11:32430439 | A | AGAGAGAG others(9): Show |
5 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(2): Show |
5 | HG01070.hp2 HG01243.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-1821_662-1820i others(18): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430439 | |||||||
chr11:32430441 | A | AGAGAGAG others(7): Show |
4 | a0001c0001t0002g0126 a0001c0002t0004g0028 a0001c0002t0004g0029 others(1): Show |
4 | HG01943.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-1823_662-1822i others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430441 | |||||||
chr11:32430443 | A | AGAGAGGG others(5): Show |
2 | a0001c0001t0002g0124 a0001c0006t0018g0125 |
2 | HG01074.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.662-1825_662-1824i others(14): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430443 | |||||||
chr11:32430445 | A | AGAGGGAG others(3): Show |
2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | NA18983.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.662-1827_662-1826i others(12): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430445 | |||||||
chr11:32430445 | A | AGAGGGAG others(4): Show |
2 | a0001c0002t0011g0026 a0001c0002t0011g0027 |
2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.662-1827_662-1826i others(13): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430445 | |||||||
chr11:32430448 | G | GGGAGGGG others(1): Show |
3 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0014t0008g0036 |
4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1830_662-1829i others(10): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430448 | |||||||
chr11:32430449 | A | G | 2 | a0001c0001t0002g0111 a0001c0001t0002g0112 |
2 | NA18965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.662-1830T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430449 | |||||||
chr11:32430451 | G | A | 118 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(115): Show |
123 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.662-1832C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430451 | |||||||
chr11:32430451 | G | GAGGGAGA others(6): Show |
1 | a0001c0001t0002g0127 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.662-1833_662-1832i others(15): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430451 | |||||||
chr11:32430453 | A | G | 2 | a0001c0001t0002g0111 a0001c0001t0002g0112 |
2 | NA18965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.662-1834T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430453 | |||||||
chr11:32430455 | G | A | 117 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(114): Show |
122 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.662-1836C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GAGAGAGA others(6): Show |
3 | a0001c0004t0009g0287 a0001c0008t0003g0288 a0001c0008t0003g0289 |
3 | HG02630.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.662-1837_662-1836i others(15): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GAGAGAGA others(8): Show |
2 | a0001c0003t0003g0246 a0001c0004t0003g0292 |
2 | HG01261.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.662-1837_662-1836i others(17): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GAGAGAGA others(10): Show |
1 | a0001c0003t0006g0224 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.662-1837_662-1836i others(19): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GAGAGAGA others(12): Show |
1 | a0001c0010t0014g0268 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.662-1837_662-1836i others(21): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GAGAGAGA others(14): Show |
1 | a0001c0004t0003g0272 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.662-1837_662-1836i others(23): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GAGAGAGA others(22): Show |
1 | a0001c0004t0004g0297 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.662-1837_662-1836i others(31): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGA | 3 | a0001c0002t0001g0007 a0001c0003t0003g0213 a0001c0003t0032g0229 |
4 | HG00639.hp2 HG01243.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-1838_662-1837d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGA | 6 | a0001c0002t0015g0056 a0001c0004t0001g0015 a0001c0004t0001g0279 others(3): Show |
7 | HG00741.hp2 HG01358.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-1840_662-1837d others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGA | 8 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0003g0214 others(5): Show |
8 | HG01169.hp2 HG01256.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.662-1842_662-1837d others(8): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGAG others(1): Show |
11 | a0001c0003t0009g0234 a0001c0003t0009g0235 a0001c0003t0010g0018 others(8): Show |
11 | HG01099.hp1 HG01175.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.662-1844_662-1837d others(10): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGAG others(3): Show |
2 | a0001c0003t0003g0237 a0001c0003t0004g0236 |
2 | HG03017.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.662-1846_662-1837d others(12): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGAG others(5): Show |
4 | a0001c0003t0004g0238 a0001c0003t0004g0239 a0001c0004t0007g0304 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-1848_662-1837d others(14): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGAG others(7): Show |
9 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0004g0240 others(6): Show |
10 | HG00642.hp1 HG01361.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.662-1850_662-1837d others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGAG others(9): Show |
13 | a0001c0002t0001g0107 a0001c0003t0001g0267 a0001c0003t0003g0244 others(10): Show |
14 | HG00733.hp2 HG01261.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.662-1852_662-1837d others(18): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGAG others(11): Show |
6 | a0001c0003t0003g0247 a0001c0003t0006g0222 a0001c0003t0006g0251 others(3): Show |
6 | HG02145.hp2 HG02976.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.662-1854_662-1837d others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGAG others(13): Show |
6 | a0001c0003t0003g0248 a0001c0003t0006g0225 a0001c0003t0006g0226 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.662-1856_662-1837d others(22): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGAG others(15): Show |
4 | a0001c0003t0003g0250 a0001c0003t0031g0249 a0001c0010t0014g0270 others(1): Show |
4 | HG02486.hp1 HG02965.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1858_662-1837d others(24): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGAGAGAG others(17): Show |
1 | a0001c0008t0003g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.662-1860_662-1837d others(26): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGGGAGAG others(7): Show |
1 | a0001c0005t0002g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.662-1837_662-1836i others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGGGAGAG others(11): Show |
1 | a0001c0003t0001g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.662-1837_662-1836i others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | G | GGGGAGAG others(15): Show |
1 | a0001c0005t0002g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.662-1837_662-1836i others(24): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | GGA | G | 14 | a0001c0002t0001g0055 a0001c0002t0001g0097 a0001c0002t0001g0098 others(11): Show |
14 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(11): Show |
intron_variant | MODIFIER | c.662-1838_662-1837d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | GGAGA | G | 68 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0005 others(65): Show |
75 | HG00408.hp2 HG00558.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.662-1840_662-1837d others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430455 | GGAGAGAG others(1): Show |
G | 3 | a0001c0003t0002g0227 a0001c0003t0004g0012 a0001c0003t0004g0013 |
5 | HG02723.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-1844_662-1837d others(10): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | |||||||
chr11:32430459 | A | G | 1 | a0001c0002t0001g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.662-1840T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430459 | |||||||
chr11:32430463 | A | G | 1 | a0001c0002t0001g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.662-1844T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430463 | |||||||
chr11:32430477 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.662-1858T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430477 | |||||||
chr11:32430486 | G | C | 1 | a0001c0004t0003g0272 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.662-1867C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | |||||||
chr11:32430486 | G | GAGAGAGA others(7): Show |
1 | a0001c0016t0016g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.662-1868_662-1867i others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | |||||||
chr11:32430486 | G | GAGAGAGA others(11): Show |
1 | a0001c0004t0003g0302 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.662-1868_662-1867i others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | |||||||
chr11:32430486 | G | GAGAGAGA others(13): Show |
2 | a0001c0004t0003g0017 a0001c0004t0003g0299 |
3 | HG00735.hp1 HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.662-1868_662-1867i others(22): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | |||||||
chr11:32430486 | G | GAGAGAGA others(17): Show |
1 | a0001c0004t0030g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.662-1868_662-1867i others(26): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | |||||||
chr11:32430491 | A | G | 3 | a0001c0003t0001g0253 a0001c0005t0002g0212 a0001c0005t0002g0252 |
3 | HG01884.hp1 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.662-1872T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430491 | |||||||
chr11:32430492 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.662-1873G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430492 | |||||||
chr11:32430545 | AGC | A | 13 | a0001c0003t0003g0213 a0001c0003t0003g0214 a0001c0003t0006g0218 others(10): Show |
13 | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.662-1928_662-1927d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430545 | |||||||
chr11:32430694 | GC | G | 107 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(104): Show |
111 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.662-2076delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430694 | |||||||
chr11:32430792 | C | T | 12 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(9): Show |
13 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-2173G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430792 | |||||||
chr11:32430929 | G | A | 11 | a0001c0002t0001g0005 a0001c0002t0001g0037 a0001c0002t0001g0038 others(8): Show |
12 | HG00408.hp1 HG00438.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.662-2310C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430929 | |||||||
chr11:32430978 | G | C | 107 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(104): Show |
111 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.662-2359C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430978 | |||||||
chr11:32431032 | C | T | 1 | a0001c0013t0001g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.662-2413G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431032 | |||||||
chr11:32431052 | G | C | 1 | a0001c0005t0002g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.662-2433C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431052 | |||||||
chr11:32431143 | C | A | 1 | a0001c0005t0002g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.662-2524G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431143 | |||||||
chr11:32431288 | G | T | 12 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(9): Show |
13 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-2669C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431288 | |||||||
chr11:32431342 | C | T | 102 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(99): Show |
108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.662-2723G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431342 | |||||||
chr11:32431379 | C | G | 232 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(229): Show |
244 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(241): Show |
intron_variant | MODIFIER | c.662-2760G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431379 | |||||||
chr11:32431399 | C | G | 102 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(99): Show |
108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.662-2780G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431399 | |||||||
chr11:32431426 | G | A | 4 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(1): Show |
4 | NA18964.hp2 NA18981.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-2807C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431426 | |||||||
chr11:32431434 | C | CT | 21 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(18): Show |
21 | HG01175.hp2 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.662-2816dupA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431434 | |||||||
chr11:32431444 | T | G | 1 | a0001c0004t0020g0301 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.662-2825A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431444 | |||||||
chr11:32431450 | TTTC | T | 36 | a0001c0002t0011g0027 a0001c0004t0001g0015 a0001c0004t0001g0279 others(33): Show |
39 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.662-2834_662-2832d others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431450 | |||||||
chr11:32431451 | TTC | T | 52 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0007g0044 others(49): Show |
55 | HG00408.hp1 HG00438.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.662-2834_662-2833d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431451 | |||||||
chr11:32431452 | TC | T | 121 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(118): Show |
126 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.662-2834delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431452 | |||||||
chr11:32431453 | C | T | 23 | a0001c0001t0002g0010 a0001c0001t0002g0142 a0001c0002t0001g0042 others(20): Show |
23 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.662-2834G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431453 | |||||||
chr11:32431476 | G | T | 2 | a0001c0010t0006g0216 a0001c0010t0021g0215 |
2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.662-2857C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431476 | |||||||
chr11:32431485 | G | T | 3 | a0001c0004t0007g0275 a0001c0004t0007g0276 a0001c0004t0007g0277 |
3 | NA18942.hp2 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.662-2866C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431485 | |||||||
chr11:32431603 | AT | A | 226 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(223): Show |
237 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.662-2985delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431603 | |||||||
chr11:32431643 | G | A | 1 | a0001c0004t0003g0302 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.662-3024C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431643 | |||||||
chr11:32431808 | C | A | 1 | a0001c0001t0002g0207 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.661+2892G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431808 | |||||||
chr11:32431867 | C | T | 2 | a0001c0010t0006g0216 a0001c0010t0021g0215 |
2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.661+2833G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431867 | |||||||
chr11:32431990 | C | T | 119 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(116): Show |
124 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.661+2710G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431990 | |||||||
chr11:32432057 | A | C | 1 | a0001c0001t0002g0120 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.661+2643T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432057 | |||||||
chr11:32432076 | G | A | 102 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(99): Show |
108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.661+2624C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432076 | |||||||
chr11:32432221 | T | C | 1 | a0001c0003t0001g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.661+2479A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432221 | |||||||
chr11:32432276 | C | T | 2 | a0001c0004t0004g0273 a0001c0004t0004g0274 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.661+2424G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432276 | |||||||
chr11:32432409 | G | C | 2 | a0001c0004t0007g0303 a0001c0004t0007g0304 |
2 | NA18947.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.661+2291C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432409 | |||||||
chr11:32432442 | C | T | 11 | a0001c0001t0002g0009 a0001c0001t0002g0111 a0001c0001t0002g0112 others(8): Show |
13 | HG02015.hp1 HG02258.hp2 HG04184.hp1 others(10): Show |
intron_variant | MODIFIER | c.661+2258G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432442 | |||||||
chr11:32432487 | G | C | 3 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0014t0008g0036 |
4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+2213C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432487 | |||||||
chr11:32432670 | C | T | 2 | a0001c0003t0003g0213 a0001c0003t0003g0214 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.661+2030G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432670 | |||||||
chr11:32432716 | G | A | 102 | a0001c0003t0001g0230 a0001c0003t0001g0231 a0001c0003t0001g0253 others(99): Show |
108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.661+1984C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432716 | |||||||
chr11:32432753 | G | A | 5 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0011t0001g0022 others(2): Show |
5 | HG01106.hp2 HG01928.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+1947C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432753 | |||||||
chr11:32432803 | A | G | 1 | a0001c0004t0003g0272 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.661+1897T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432803 | |||||||
chr11:32432996 | C | G | 2 | a0001c0009t0008g0031 a0001c0009t0008g0032 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.661+1704G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432996 | |||||||
chr11:32433056 | T | A | 1 | a0001c0001t0002g0208 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.661+1644A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433056 | |||||||
chr11:32433136 | C | T | 3 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0014t0008g0036 |
4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+1564G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433136 | |||||||
chr11:32433366 | C | T | 1 | a0001c0004t0003g0271 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.661+1334G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433366 | |||||||
chr11:32433371 | G | T | 5 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0011g0026 others(2): Show |
5 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+1329C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433371 | |||||||
chr11:32433464 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.661+1236G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433464 | |||||||
chr11:32433519 | C | T | 11 | a0001c0002t0001g0005 a0001c0002t0001g0037 a0001c0002t0001g0038 others(8): Show |
12 | HG00408.hp1 HG00438.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.661+1181G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433519 | |||||||
chr11:32433981 | C | A | 221 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(218): Show |
232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.661+719G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433981 | |||||||
chr11:32434015 | C | A | 3 | a0001c0006t0001g0211 a0001c0012t0014g0210 a0001c0012t0023g0209 |
3 | HG02257.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.661+685G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434015 | |||||||
chr11:32434037 | G | C | 3 | a0001c0009t0008g0004 a0001c0009t0008g0035 a0001c0014t0008g0036 |
4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+663C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434037 | |||||||
chr11:32434307 | G | T | 119 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(116): Show |
124 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.661+393C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434307 | |||||||
chr11:32434480 | C | T | 1 | a0001c0005t0002g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.661+220G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434480 | |||||||
chr11:32434539 | C | A | 17 | a0001c0003t0001g0256 a0001c0003t0001g0263 a0001c0003t0001g0267 others(14): Show |
17 | HG01109.hp2 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.661+161G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434539 |