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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g02040 A02 903514 C T synonymous_variant LOW c.214C>T|p.Leu72Leu S262
2 BAA02g02040 A02 903976 G A synonymous_variant LOW c.411G>A|p.Ser137Ser S219
S72
3 BAA02g02040 A02 904710 C T synonymous_variant LOW c.687C>T|p.Gly229Gly S33
4 BAA02g02040 A02 904910 G A missense_variant MODERATE c.772G>A|p.Glu258Lys S176
5 BAA02g02040 A02 905183 G A missense_variant MODERATE c.808G>A|p.Val270Met S247
6 BAA02g02040 A02 905205 G A missense_variant MODERATE c.830G>A|p.Arg277His S202
7 BAA02g02040 A02 905208 C T missense_variant MODERATE c.833C>T|p.Ser278Phe S177
8 BAA02g02040 A02 905286 G A missense_variant MODERATE c.911G>A|p.Gly304Glu S255
9 BAA02g02040 A02 906105 G A missense_variant MODERATE c.991G>A|p.Glu331Lys S132
S137
S215
10 BAA02g02040 A02 907933 C T missense_variant MODERATE c.1775C>T|p.Ala592Val S56
11 BAA02g02040 A02 908400 G A missense_variant MODERATE c.1988G>A|p.Gly663Asp S67
12 BAA02g02040 A02 909043 C T splice_region_variant&intron_variant LOW c.2166-3C>T| S229
13 BAA02g02040 A02 910901 C T synonymous_variant LOW c.3150C>T|p.Phe1050Phe S94
14 BAA02g02040 A02 910914 G A downstream_gene_variant MODIFIER c.*1G>A| S293