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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g16920 A02 8375170 G A upstream_gene_variant MODIFIER c.-4888G>A| S59
2 BAA02g16920 A02 8375197 G A upstream_gene_variant MODIFIER c.-4861G>A| S87
3 BAA02g16920 A02 8375239 C T upstream_gene_variant MODIFIER c.-4819C>T| S25
4 BAA02g16920 A02 8376035 G A upstream_gene_variant MODIFIER c.-4023G>A| S274
5 BAA02g16920 A02 8376140 G A upstream_gene_variant MODIFIER c.-3918G>A| S95
6 BAA02g16920 A02 8376319 G A upstream_gene_variant MODIFIER c.-3739G>A| S272
7 BAA02g16920 A02 8377186 C T upstream_gene_variant MODIFIER c.-2872C>T| S9
8 BAA02g16920 A02 8377627 G A upstream_gene_variant MODIFIER c.-2431G>A| S274
9 BAA02g16920 A02 8377978 C T upstream_gene_variant MODIFIER c.-2080C>T| S78
10 BAA02g16920 A02 8378145 C T upstream_gene_variant MODIFIER c.-1913C>T| S92
11 BAA02g16920 A02 8379499 C T upstream_gene_variant MODIFIER c.-559C>T| S81
S85
12 BAA02g16920 A02 8379776 G A upstream_gene_variant MODIFIER c.-282G>A| S269
13 BAA02g16920 A02 8380113 C T missense_variant MODERATE c.56C>T|p.Ser19Leu S275
14 BAA02g16920 A02 8380483 C T synonymous_variant LOW c.426C>T|p.Thr142Thr S208
S219
15 BAA02g16920 A02 8380828 G A synonymous_variant LOW c.771G>A|p.Glu257Glu S197
16 BAA02g16920 A02 8381483 G A downstream_gene_variant MODIFIER c.*412G>A| S43
17 BAA02g16920 A02 8381993 C T downstream_gene_variant MODIFIER c.*922C>T| S65
18 BAA02g16920 A02 8382229 C T downstream_gene_variant MODIFIER c.*1158C>T| S13
19 BAA02g16920 A02 8382524 G A downstream_gene_variant MODIFIER c.*1453G>A| S157
20 BAA02g16920 A02 8383379 C T downstream_gene_variant MODIFIER c.*2308C>T| S241
21 BAA02g16920 A02 8383435 C T downstream_gene_variant MODIFIER c.*2364C>T| S268
22 BAA02g16920 A02 8384849 G A downstream_gene_variant MODIFIER c.*3778G>A| S170
23 BAA02g16920 A02 8385943 G A downstream_gene_variant MODIFIER c.*4872G>A| S149