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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g36940 A06 24398583 C T synonymous_variant LOW c.117C>T|p.Ile39Ile S4
2 BAA06g36940 A06 24399055 G A missense_variant MODERATE c.490G>A|p.Asp164Asn S38
3 BAA06g36940 A06 24399829 C T missense_variant MODERATE c.781C>T|p.Pro261Ser S252
4 BAA06g36940 A06 24400030 G A synonymous_variant LOW c.864G>A|p.Lys288Lys S197
5 BAA06g36940 A06 24400323 G A splice_region_variant&intron_variant LOW c.967-4G>A| S103
6 BAA06g36940 A06 24400660 C T missense_variant MODERATE c.1220C>T|p.Pro407Leu S213
7 BAA06g36940 A06 24400846 C T missense_variant MODERATE c.1319C>T|p.Ser440Phe S207
8 BAA06g36940 A06 24400871 C T synonymous_variant LOW c.1344C>T|p.Tyr448Tyr S244
9 BAA06g36940 A06 24402611 G A downstream_gene_variant MODIFIER c.*1528G>A| S60
10 BAA06g36940 A06 24402853 G A downstream_gene_variant MODIFIER c.*1770G>A| S210
S225
11 BAA06g36940 A06 24403106 G A downstream_gene_variant MODIFIER c.*2023G>A| S56
12 BAA06g36940 A06 24403829 C T downstream_gene_variant MODIFIER c.*2746C>T| S104
S52
13 BAA06g36940 A06 24404100 C T downstream_gene_variant MODIFIER c.*3017C>T| S133