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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g45030 A02 36985611 T A missense_variant MODERATE c.3772A>T|p.Arg1258Trp
2 BAA02g45030 A02 36985764 C T missense_variant MODERATE c.3619G>A|p.Glu1207Lys S190
3 BAA02g45030 A02 36985807 G A synonymous_variant LOW c.3576C>T|p.Val1192Val S126
4 BAA02g45030 A02 36986059 A C missense_variant MODERATE c.3401T>G|p.Leu1134Arg S114
S137
S223
S306
S54
5 BAA02g45030 A02 36986191 G A missense_variant MODERATE c.3269C>T|p.Ala1090Val S155
S211
6 BAA02g45030 A02 36986544 G A synonymous_variant LOW c.2916C>T|p.Asp972Asp S2
7 BAA02g45030 A02 36986583 G A splice_region_variant&synonymous_variant LOW c.2877C>T|p.Ala959Ala S223
8 BAA02g45030 A02 36987138 C T missense_variant MODERATE c.2513G>A|p.Arg838Lys S242
9 BAA02g45030 A02 36990095 C T missense_variant MODERATE c.1073G>A|p.Arg358His S299
10 BAA02g45030 A02 36991007 C T missense_variant MODERATE c.619G>A|p.Gly207Ser S228
11 BAA02g45030 A02 36991445 C T splice_region_variant&intron_variant LOW c.259-5G>A| S64
12 BAA02g45030 A02 36993298 G A upstream_gene_variant MODIFIER c.-788C>T| S36
13 BAA02g45030 A02 36993580 G A upstream_gene_variant MODIFIER c.-1070C>T| S292
14 BAA02g45030 A02 36993976 G A upstream_gene_variant MODIFIER c.-1466C>T| S111
15 BAA02g45030 A02 36995475 C T upstream_gene_variant MODIFIER c.-2965G>A| S115
16 BAA02g45030 A02 36997438 G A upstream_gene_variant MODIFIER c.-4928C>T| S155
S211