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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g31150 A09 38434823 A T upstream_gene_variant MODIFIER c.-1740A>T| S121
2 BAA09g31150 A09 38435172 G A upstream_gene_variant MODIFIER c.-1391G>A| S208
S219
3 BAA09g31150 A09 38436214 C T upstream_gene_variant MODIFIER c.-349C>T| S12
S258
4 BAA09g31150 A09 38437048 C T intron_variant MODIFIER c.269+115C>T| S221
5 BAA09g31150 A09 38437108 C T intron_variant MODIFIER c.269+175C>T| S150
6 BAA09g31150 A09 38437808 G A intron_variant MODIFIER c.418-24G>A| S9
7 BAA09g31150 A09 38437818 C T intron_variant MODIFIER c.418-14C>T| S166
8 BAA09g31150 A09 38437921 C T synonymous_variant LOW c.507C>T|p.Pro169Pro S87
9 BAA09g31150 A09 38437932 G A missense_variant MODERATE c.518G>A|p.Gly173Glu S32
10 BAA09g31150 A09 38438196 G A intron_variant MODIFIER c.672+12G>A| S58
11 BAA09g31150 A09 38438368 G A missense_variant MODERATE c.710G>A|p.Arg237His S144
12 BAA09g31150 A09 38438558 C T intron_variant MODIFIER c.831-23C>T| S124
13 BAA09g31150 A09 38438826 G A intron_variant MODIFIER c.944-12G>A| S1
S90
14 BAA09g31150 A09 38438841 G A missense_variant MODERATE c.947G>A|p.Gly316Asp S32
15 BAA09g31150 A09 38438893 C T synonymous_variant LOW c.999C>T|p.Thr333Thr S200
16 BAA09g31150 A09 38440044 G A downstream_gene_variant MODIFIER c.*879G>A| S1
17 BAA09g31150 A09 38440174 G A downstream_gene_variant MODIFIER c.*1009G>A| S302
18 BAA09g31150 A09 38440346 C T downstream_gene_variant MODIFIER c.*1181C>T| S262