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 BAA09g17530 A09 10493041 C T upstream_gene_variant MODIFIER c.-4353C>T| S18
2 BAA09g17530 A09 10493871 G A upstream_gene_variant MODIFIER c.-3523G>A| S126
3 BAA09g17530 A09 10494348 G A upstream_gene_variant MODIFIER c.-3046G>A| S121
4 BAA09g17530 A09 10494352 G A upstream_gene_variant MODIFIER c.-3042G>A| S155
S211
5 BAA09g17530 A09 10494434 C T upstream_gene_variant MODIFIER c.-2960C>T| S122
6 BAA09g17530 A09 10494608 C T upstream_gene_variant MODIFIER c.-2786C>T| S125
7 BAA09g17530 A09 10495008 G A upstream_gene_variant MODIFIER c.-2386G>A| S171
8 BAA09g17530 A09 10495547 G A upstream_gene_variant MODIFIER c.-1847G>A| S1
9 BAA09g17530 A09 10497772 C T intron_variant MODIFIER c.37-96C>T| S132
S137
10 BAA09g17530 A09 10498110 G A synonymous_variant LOW c.279G>A|p.Lys93Lys S57
11 BAA09g17530 A09 10499684 C T missense_variant MODERATE c.1603C>T|p.Pro535Ser S39
12 BAA09g17530 A09 10501003 G A missense_variant MODERATE c.2671G>A|p.Ala891Thr S271
13 BAA09g17530 A09 10501302 C T downstream_gene_variant MODIFIER c.*264C>T| S186
S228
14 BAA09g17530 A09 10501698 C T downstream_gene_variant MODIFIER c.*660C>T| S119