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 BAA02g28980 A02 16461136 C T missense_variant MODERATE c.515C>T|p.Pro172Leu S122
2 BAA02g28980 A02 16461347 G A synonymous_variant LOW c.726G>A|p.Leu242Leu S62
3 BAA02g28980 A02 16462165 G A downstream_gene_variant MODIFIER c.*527G>A| S247
4 BAA02g28980 A02 16462808 G A downstream_gene_variant MODIFIER c.*1170G>A| S209
5 BAA02g28980 A02 16462816 C T downstream_gene_variant MODIFIER c.*1178C>T| S112
6 BAA02g28980 A02 16463031 G A downstream_gene_variant MODIFIER c.*1393G>A| S207
7 BAA02g28980 A02 16463608 C T downstream_gene_variant MODIFIER c.*1970C>T| S204
8 BAA02g28980 A02 16464307 G A downstream_gene_variant MODIFIER c.*2669G>A| S169
9 BAA02g28980 A02 16464381 G A downstream_gene_variant MODIFIER c.*2743G>A| S80
10 BAA02g28980 A02 16464499 C T downstream_gene_variant MODIFIER c.*2861C>T| S193
11 BAA02g28980 A02 16464645 G A downstream_gene_variant MODIFIER c.*3007G>A| S23
S293
12 BAA02g28980 A02 16464835 C T downstream_gene_variant MODIFIER c.*3197C>T| S283
13 BAA02g28980 A02 16464858 C T downstream_gene_variant MODIFIER c.*3220C>T| S2
14 BAA02g28980 A02 16464912 C T downstream_gene_variant MODIFIER c.*3274C>T| S51
15 BAA02g28980 A02 16465269 C T downstream_gene_variant MODIFIER c.*3631C>T| S167
16 BAA02g28980 A02 16465997 C T downstream_gene_variant MODIFIER c.*4359C>T| S308
17 BAA02g28980 A02 16466214 G A downstream_gene_variant MODIFIER c.*4576G>A| S116
S161
18 BAA02g28980 A02 16466458 C T downstream_gene_variant MODIFIER c.*4820C>T| S15