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 BAA02g41610 A02 34870977 G A upstream_gene_variant MODIFIER c.-2502G>A| S11
2 BAA02g41610 A02 34871670 C T upstream_gene_variant MODIFIER c.-1809C>T| S283
3 BAA02g41610 A02 34872344 G A upstream_gene_variant MODIFIER c.-1135G>A| S168
4 BAA02g41610 A02 34872801 C T upstream_gene_variant MODIFIER c.-678C>T| S68
5 BAA02g41610 A02 34873571 C T synonymous_variant LOW c.93C>T|p.Phe31Phe S201
6 BAA02g41610 A02 34873773 G A missense_variant MODERATE c.295G>A|p.Asp99Asn S255
7 BAA02g41610 A02 34873776 C T synonymous_variant LOW c.298C>T|p.Leu100Leu S63
8 BAA02g41610 A02 34874933 G A missense_variant MODERATE c.686G>A|p.Arg229Lys S36
9 BAA02g41610 A02 34875450 G A synonymous_variant LOW c.1203G>A|p.Glu401Glu S134
10 BAA02g41610 A02 34876453 G A intron_variant MODIFIER c.1875+215G>A| S36
11 BAA02g41610 A02 34877104 C T intron_variant MODIFIER c.1875+866C>T| S275
S301
S304
12 BAA02g41610 A02 34879193 G A intron_variant MODIFIER c.1876-2936G>A| S60
13 BAA02g41610 A02 34879671 C T intron_variant MODIFIER c.1876-2458C>T| S42
14 BAA02g41610 A02 34879839 G A intron_variant MODIFIER c.1876-2290G>A| S69
15 BAA02g41610 A02 34879940 G A intron_variant MODIFIER c.1876-2189G>A| S293
16 BAA02g41610 A02 34880577 C T intron_variant MODIFIER c.1876-1552C>T| S178
17 BAA02g41610 A02 34888343 G A downstream_gene_variant MODIFIER c.*3793G>A| S302