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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g08350 A10 10078952 G A downstream_gene_variant MODIFIER c.*3456C>T| S206
2 BAA10g08350 A10 10079131 C T downstream_gene_variant MODIFIER c.*3277G>A| S193
3 BAA10g08350 A10 10079325 G A downstream_gene_variant MODIFIER c.*3083C>T| S18
4 BAA10g08350 A10 10079934 G A downstream_gene_variant MODIFIER c.*2474C>T| S66
5 BAA10g08350 A10 10080617 C T downstream_gene_variant MODIFIER c.*1791G>A| S68
6 BAA10g08350 A10 10081392 G A downstream_gene_variant MODIFIER c.*1016C>T| S251
7 BAA10g08350 A10 10082342 G A downstream_gene_variant MODIFIER c.*66C>T| S15
S3
8 BAA10g08350 A10 10082760 C T missense_variant MODERATE c.1052G>A|p.Gly351Glu S25
9 BAA10g08350 A10 10083711 C T intron_variant MODIFIER c.902-801G>A| S270
10 BAA10g08350 A10 10083987 C T intron_variant MODIFIER c.902-1077G>A| S169
11 BAA10g08350 A10 10084127 G A intron_variant MODIFIER c.902-1217C>T| S234
12 BAA10g08350 A10 10084569 C T intron_variant MODIFIER c.901+867G>A| S144
13 BAA10g08350 A10 10085481 G A missense_variant MODERATE c.856C>T|p.Pro286Ser S221
14 BAA10g08350 A10 10085865 C T missense_variant MODERATE c.472G>A|p.Val158Ile S188
S265
15 BAA10g08350 A10 10086204 G A missense_variant MODERATE c.133C>T|p.Pro45Ser S172
S217