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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g66750 A03 41212397 C T downstream_gene_variant MODIFIER c.*1159G>A| S86
2 BAA03g66750 A03 41212602 C T downstream_gene_variant MODIFIER c.*954G>A| S192
3 BAA03g66750 A03 41214361 G A intron_variant MODIFIER c.1665+323C>T| S168
4 BAA03g66750 A03 41214371 C T intron_variant MODIFIER c.1665+313G>A| S23
5 BAA03g66750 A03 41214834 C T missense_variant MODERATE c.1607G>A|p.Gly536Glu S185
6 BAA03g66750 A03 41214870 G A missense_variant MODERATE c.1571C>T|p.Ser524Leu S46
7 BAA03g66750 A03 41215115 C T stop_gained HIGH c.1395G>A|p.Trp465* S200
8 BAA03g66750 A03 41215843 C T missense_variant MODERATE c.763G>A|p.Val255Ile S95
9 BAA03g66750 A03 41215955 C T stop_gained HIGH c.651G>A|p.Trp217* S218
10 BAA03g66750 A03 41216027 C T synonymous_variant LOW c.579G>A|p.Gly193Gly S172
S217
11 BAA03g66750 A03 41216064 G A missense_variant MODERATE c.542C>T|p.Ser181Phe S221
12 BAA03g66750 A03 41216104 G A missense_variant MODERATE c.502C>T|p.Pro168Ser S230
13 BAA03g66750 A03 41216498 G A synonymous_variant LOW c.108C>T|p.Leu36Leu S178
14 BAA03g66750 A03 41217226 G A upstream_gene_variant MODIFIER c.-621C>T| S138
15 BAA03g66750 A03 41217264 G A upstream_gene_variant MODIFIER c.-659C>T| S143
16 BAA03g66750 A03 41219351 G A upstream_gene_variant MODIFIER c.-2746C>T| S96
17 BAA03g66750 A03 41220239 G A upstream_gene_variant MODIFIER c.-3634C>T| S168
18 BAA03g66750 A03 41220283 C T upstream_gene_variant MODIFIER c.-3678G>A| S2
19 BAA03g66750 A03 41220510 G A upstream_gene_variant MODIFIER c.-3905C>T| S148
20 BAA03g66750 A03 41221196 C T upstream_gene_variant MODIFIER c.-4591G>A| S100
21 BAA03g66750 A03 41221203 G A upstream_gene_variant MODIFIER c.-4598C>T| S217
S248