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 BAA02g31320 A02 18818862 G A missense_variant MODERATE c.665C>T|p.Pro222Leu S55
2 BAA02g31320 A02 18819389 C T missense_variant MODERATE c.372G>A|p.Met124Ile S277
3 BAA02g31320 A02 18819713 C T missense_variant MODERATE c.175G>A|p.Asp59Asn S165
4 BAA02g31320 A02 18819758 C T missense_variant MODERATE c.130G>A|p.Gly44Arg S152
5 BAA02g31320 A02 18819762 G A splice_region_variant&synonymous_variant LOW c.126C>T|p.Asp42Asp S188
6 BAA02g31320 A02 18820447 G A upstream_gene_variant MODIFIER c.-437C>T| S41
7 BAA02g31320 A02 18820645 C T upstream_gene_variant MODIFIER c.-635G>A| S54
8 BAA02g31320 A02 18820724 C T upstream_gene_variant MODIFIER c.-714G>A| S282
9 BAA02g31320 A02 18820750 G A upstream_gene_variant MODIFIER c.-740C>T| S160
10 BAA02g31320 A02 18821344 G A upstream_gene_variant MODIFIER c.-1334C>T| S271
11 BAA02g31320 A02 18821769 G T upstream_gene_variant MODIFIER c.-1759C>A| S178
12 BAA02g31320 A02 18821806 G A upstream_gene_variant MODIFIER c.-1796C>T| S134
13 BAA02g31320 A02 18822184 G A upstream_gene_variant MODIFIER c.-2174C>T| S210
14 BAA02g31320 A02 18822200 C T upstream_gene_variant MODIFIER c.-2190G>A| S257
15 BAA02g31320 A02 18822285 C T upstream_gene_variant MODIFIER c.-2275G>A| S232
16 BAA02g31320 A02 18822912 G A upstream_gene_variant MODIFIER c.-2902C>T| S153
S213
17 BAA02g31320 A02 18822928 G A upstream_gene_variant MODIFIER c.-2918C>T| S228
18 BAA02g31320 A02 18822945 G A upstream_gene_variant MODIFIER c.-2935C>T| S302
19 BAA02g31320 A02 18823312 G A upstream_gene_variant MODIFIER c.-3302C>T| S293
20 BAA02g31320 A02 18823610 C T upstream_gene_variant MODIFIER c.-3600G>A| S142
21 BAA02g31320 A02 18823705 G A upstream_gene_variant MODIFIER c.-3695C>T| S236
22 BAA02g31320 A02 18824930 C T upstream_gene_variant MODIFIER c.-4920G>A| S53
23 BAA02g31320 A02 18824939 C T upstream_gene_variant MODIFIER c.-4929G>A| S282