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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g65990 A03 40305773 C T upstream_gene_variant MODIFIER c.-3732C>T| S164
2 BAA03g65990 A03 40305783 C T upstream_gene_variant MODIFIER c.-3722C>T| S241
3 BAA03g65990 A03 40305988 C T upstream_gene_variant MODIFIER c.-3517C>T| S20
4 BAA03g65990 A03 40306023 G A upstream_gene_variant MODIFIER c.-3482G>A| S202
5 BAA03g65990 A03 40306455 G A upstream_gene_variant MODIFIER c.-3050G>A| S111
6 BAA03g65990 A03 40306561 C T upstream_gene_variant MODIFIER c.-2944C>T| S195
7 BAA03g65990 A03 40307027 C T upstream_gene_variant MODIFIER c.-2478C>T| S172
S217
8 BAA03g65990 A03 40307233 G A upstream_gene_variant MODIFIER c.-2272G>A| S218
9 BAA03g65990 A03 40308181 G A upstream_gene_variant MODIFIER c.-1324G>A| S202
10 BAA03g65990 A03 40308496 G A upstream_gene_variant MODIFIER c.-1009G>A| S67
11 BAA03g65990 A03 40308704 C T upstream_gene_variant MODIFIER c.-801C>T| S180
12 BAA03g65990 A03 40310094 G A intron_variant MODIFIER c.352-50G>A| S308
13 BAA03g65990 A03 40310564 G A synonymous_variant LOW c.678G>A|p.Lys226Lys S56
14 BAA03g65990 A03 40310653 G A missense_variant MODERATE c.767G>A|p.Gly256Glu S135
15 BAA03g65990 A03 40310749 A T intron_variant MODIFIER c.825+38A>T| S197
16 BAA03g65990 A03 40312040 G A downstream_gene_variant MODIFIER c.*166G>A| S81
S85
17 BAA03g65990 A03 40312053 C T downstream_gene_variant MODIFIER c.*179C>T| S163