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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g31350 A02 18826753 C T upstream_gene_variant MODIFIER c.-4650C>T| S79
S91
2 BAA02g31350 A02 18827225 G A upstream_gene_variant MODIFIER c.-4178G>A| S229
3 BAA02g31350 A02 18827841 G A upstream_gene_variant MODIFIER c.-3562G>A| S133
4 BAA02g31350 A02 18828230 G A upstream_gene_variant MODIFIER c.-3173G>A| S35
5 BAA02g31350 A02 18828509 C T upstream_gene_variant MODIFIER c.-2894C>T| S206
6 BAA02g31350 A02 18831416 G A missense_variant MODERATE c.14G>A|p.Gly5Glu S17
S47
7 BAA02g31350 A02 18831639 G A stop_gained HIGH c.237G>A|p.Trp79* S259
8 BAA02g31350 A02 18832794 C T missense_variant MODERATE c.1100C>T|p.Ser367Phe S39
9 BAA02g31350 A02 18832840 G A synonymous_variant LOW c.1146G>A|p.Gln382Gln S60
10 BAA02g31350 A02 18832883 G A missense_variant MODERATE c.1189G>A|p.Gly397Ser S133
11 BAA02g31350 A02 18832931 G A missense_variant MODERATE c.1237G>A|p.Val413Ile S95
12 BAA02g31350 A02 18833034 G A missense_variant&splice_region_variant MODERATE c.1340G>A|p.Gly447Glu S256
13 BAA02g31350 A02 18833881 C T splice_region_variant&intron_variant LOW c.1767+7C>T| S172
S217
14 BAA02g31350 A02 18834448 C T missense_variant MODERATE c.1960C>T|p.His654Tyr S23
15 BAA02g31350 A02 18834685 G A synonymous_variant LOW c.2148G>A|p.Ala716Ala S136
16 BAA02g31350 A02 18834895 G A missense_variant MODERATE c.2305G>A|p.Glu769Lys S245
17 BAA02g31350 A02 18835265 G A downstream_gene_variant MODIFIER c.*305G>A| S235
18 BAA02g31350 A02 18835893 G A downstream_gene_variant MODIFIER c.*933G>A| S235
19 BAA02g31350 A02 18836351 C T downstream_gene_variant MODIFIER c.*1391C>T| S202
S46
S98