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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g26970 A01 15244308 C T missense_variant&splice_region_variant MODERATE c.3067G>A|p.Gly1023Arg S99
2 BAA01g26970 A01 15244362 G A stop_gained HIGH c.3013C>T|p.Gln1005* S197
3 BAA01g26970 A01 15245180 C T missense_variant MODERATE c.2492G>A|p.Arg831Lys S20
4 BAA01g26970 A01 15248452 G A missense_variant MODERATE c.1423C>T|p.His475Tyr S23
5 BAA01g26970 A01 15249672 C T synonymous_variant LOW c.369G>A|p.Glu123Glu S132
S137
S215
6 BAA01g26970 A01 15249870 C T missense_variant MODERATE c.275G>A|p.Gly92Glu S120
7 BAA01g26970 A01 15250486 C T upstream_gene_variant MODIFIER c.-239G>A| S89
8 BAA01g26970 A01 15252800 G A upstream_gene_variant MODIFIER c.-2553C>T| S63
9 BAA01g26970 A01 15252816 C T upstream_gene_variant MODIFIER c.-2569G>A| S42
10 BAA01g26970 A01 15252997 C T upstream_gene_variant MODIFIER c.-2750G>A| S302
11 BAA01g26970 A01 15253481 G A upstream_gene_variant MODIFIER c.-3234C>T| S294
12 BAA01g26970 A01 15254310 C A upstream_gene_variant MODIFIER c.-4063G>T| S86
13 BAA01g26970 A01 15254640 G A upstream_gene_variant MODIFIER c.-4393C>T| S172