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


Gene ID

Results: 1 - 39 of 39 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g33180 A09 41816774 C T upstream_gene_variant MODIFIER c.-3844C>T| S158
2 BAA09g33180 A09 41818444 C T upstream_gene_variant MODIFIER c.-2174C>T| S6
3 BAA09g33180 A09 41819589 G A upstream_gene_variant MODIFIER c.-1029G>A| S34
4 BAA09g33180 A09 41819912 G A upstream_gene_variant MODIFIER c.-706G>A| S176
5 BAA09g33180 A09 41820305 G A upstream_gene_variant MODIFIER c.-313G>A| S38
6 BAA09g33180 A09 41820430 C T upstream_gene_variant MODIFIER c.-188C>T| S146
S178
7 BAA09g33180 A09 41820675 G A missense_variant MODERATE c.58G>A|p.Gly20Ser S172
S217
8 BAA09g33180 A09 41820737 G A stop_gained HIGH c.120G>A|p.Trp40* S149
9 BAA09g33180 A09 41821035 G A intron_variant MODIFIER c.270+148G>A| S124
10 BAA09g33180 A09 41821565 G A intron_variant MODIFIER c.270+678G>A| S132
S137
S215
11 BAA09g33180 A09 41821631 C T intron_variant MODIFIER c.270+744C>T| S273
12 BAA09g33180 A09 41821707 C T intron_variant MODIFIER c.270+820C>T| S139
13 BAA09g33180 A09 41821833 C T intron_variant MODIFIER c.270+946C>T| S192
14 BAA09g33180 A09 41822837 A T intron_variant MODIFIER c.270+1950A>T| S61
15 BAA09g33180 A09 41823680 G A intron_variant MODIFIER c.270+2793G>A| S127
16 BAA09g33180 A09 41824378 G A intron_variant MODIFIER c.271-3104G>A| S178
17 BAA09g33180 A09 41825022 G A intron_variant MODIFIER c.271-2460G>A| S134
18 BAA09g33180 A09 41825074 C T intron_variant MODIFIER c.271-2408C>T| S286
19 BAA09g33180 A09 41826021 G A intron_variant MODIFIER c.271-1461G>A| S148
20 BAA09g33180 A09 41827305 G A intron_variant MODIFIER c.271-177G>A| S155
S211
21 BAA09g33180 A09 41827849 G A missense_variant MODERATE c.638G>A|p.Gly213Glu S166
22 BAA09g33180 A09 41830454 C T intron_variant MODIFIER c.812+2431C>T| S268
S269
23 BAA09g33180 A09 41832797 G A intron_variant MODIFIER c.813-623G>A| S81
S85
24 BAA09g33180 A09 41832887 C T intron_variant MODIFIER c.813-533C>T| S247
25 BAA09g33180 A09 41833019 C T intron_variant MODIFIER c.813-401C>T| S245