Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g30400 A02 17741662 C T upstream_gene_variant MODIFIER c.-1869C>T| S139
2 BAA02g30400 A02 17742171 C T upstream_gene_variant MODIFIER c.-1360C>T| S218
3 BAA02g30400 A02 17743143 C T upstream_gene_variant MODIFIER c.-388C>T| S64
4 BAA02g30400 A02 17743560 G A stop_gained HIGH c.30G>A|p.Trp10* S269
5 BAA02g30400 A02 17744137 G C missense_variant&splice_region_variant MODERATE c.425G>C|p.Ser142Thr S176
6 BAA02g30400 A02 17745362 C T intron_variant MODIFIER c.888-21C>T| S130
7 BAA02g30400 A02 17745786 C T missense_variant MODERATE c.1291C>T|p.Pro431Ser S177
8 BAA02g30400 A02 17745817 C T missense_variant MODERATE c.1322C>T|p.Ala441Val S2
9 BAA02g30400 A02 17745829 G A missense_variant MODERATE c.1334G>A|p.Arg445Lys S111
10 BAA02g30400 A02 17746189 C T downstream_gene_variant MODIFIER c.*248C>T| S65
11 BAA02g30400 A02 17747239 G A downstream_gene_variant MODIFIER c.*1298G>A| S55
12 BAA02g30400 A02 17747551 C T downstream_gene_variant MODIFIER c.*1610C>T| S92
13 BAA02g30400 A02 17748892 G A downstream_gene_variant MODIFIER c.*2951G>A| S298
14 BAA02g30400 A02 17748900 C T downstream_gene_variant MODIFIER c.*2959C>T| S246
15 BAA02g30400 A02 17749107 C T downstream_gene_variant MODIFIER c.*3166C>T| S66
16 BAA02g30400 A02 17749721 C T downstream_gene_variant MODIFIER c.*3780C>T| S100
17 BAA02g30400 A02 17750483 G A downstream_gene_variant MODIFIER c.*4542G>A| S12
18 BAA02g30400 A02 17750856 C T downstream_gene_variant MODIFIER c.*4915C>T| S157
S163