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 BAA02g16480 A02 8037090 G A downstream_gene_variant MODIFIER c.*3263C>T| S124
2 BAA02g16480 A02 8040469 C T missense_variant MODERATE c.3283G>A|p.Gly1095Arg S233
3 BAA02g16480 A02 8040773 C T synonymous_variant LOW c.2979G>A|p.Arg993Arg S120
4 BAA02g16480 A02 8040878 C T synonymous_variant LOW c.2874G>A|p.Lys958Lys S58
5 BAA02g16480 A02 8040928 C T missense_variant MODERATE c.2824G>A|p.Glu942Lys S6
6 BAA02g16480 A02 8042583 C T intron_variant MODIFIER c.2542+664G>A| S245
7 BAA02g16480 A02 8043749 C T synonymous_variant LOW c.2040G>A|p.Arg680Arg S50
8 BAA02g16480 A02 8043750 C T missense_variant MODERATE c.2039G>A|p.Arg680Gln S187
9 BAA02g16480 A02 8044601 C T missense_variant MODERATE c.1352G>A|p.Arg451Lys S78
S83
10 BAA02g16480 A02 8045018 G A missense_variant MODERATE c.935C>T|p.Ser312Leu S74
11 BAA02g16480 A02 8045184 C T missense_variant MODERATE c.769G>A|p.Glu257Lys S255
12 BAA02g16480 A02 8045265 C T missense_variant MODERATE c.688G>A|p.Val230Ile S112
13 BAA02g16480 A02 8045589 G A missense_variant MODERATE c.364C>T|p.Pro122Ser S10
14 BAA02g16480 A02 8046627 G A upstream_gene_variant MODIFIER c.-675C>T| S190
15 BAA02g16480 A02 8047037 C T upstream_gene_variant MODIFIER c.-1085G>A| S44
16 BAA02g16480 A02 8048361 C T upstream_gene_variant MODIFIER c.-2409G>A| S42
17 BAA02g16480 A02 8050754 C T upstream_gene_variant MODIFIER c.-4802G>A| S78