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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g29670 A02 17008807 C T downstream_gene_variant MODIFIER c.*2165G>A| S2
2 BAA02g29670 A02 17010354 C T downstream_gene_variant MODIFIER c.*618G>A| S138
3 BAA02g29670 A02 17010516 C T downstream_gene_variant MODIFIER c.*456G>A| S15
4 BAA02g29670 A02 17010567 C T downstream_gene_variant MODIFIER c.*405G>A| S92
5 BAA02g29670 A02 17011148 G A intron_variant MODIFIER c.2560-93C>T| S41
6 BAA02g29670 A02 17011726 C T missense_variant MODERATE c.2299G>A|p.Glu767Lys S177
7 BAA02g29670 A02 17012247 G A intron_variant MODIFIER c.2007+20C>T| S205
8 BAA02g29670 A02 17012753 G A synonymous_variant LOW c.1671C>T|p.Leu557Leu S133
9 BAA02g29670 A02 17013614 C T missense_variant MODERATE c.1117G>A|p.Ala373Thr S142
10 BAA02g29670 A02 17013915 C T stop_gained HIGH c.900G>A|p.Trp300* S266
11 BAA02g29670 A02 17014430 C T intron_variant MODIFIER c.691-20G>A| S54
12 BAA02g29670 A02 17014442 G A intron_variant MODIFIER c.691-32C>T| S38
13 BAA02g29670 A02 17015002 G A missense_variant MODERATE c.509C>T|p.Thr170Ile S245
14 BAA02g29670 A02 17015330 C T splice_donor_variant&intron_variant HIGH c.345+1G>A| S185
15 BAA02g29670 A02 17015642 G A missense_variant MODERATE c.191C>T|p.Ser64Phe S36
16 BAA02g29670 A02 17015748 G A missense_variant MODERATE c.85C>T|p.Pro29Ser S67
17 BAA02g29670 A02 17016119 G A upstream_gene_variant MODIFIER c.-287C>T| S20
18 BAA02g29670 A02 17016198 G A upstream_gene_variant MODIFIER c.-366C>T| S228
19 BAA02g29670 A02 17016251 G A upstream_gene_variant MODIFIER c.-419C>T| S223
20 BAA02g29670 A02 17016896 C T upstream_gene_variant MODIFIER c.-1064G>A| S266
21 BAA02g29670 A02 17017564 G A upstream_gene_variant MODIFIER c.-1732C>T| S263
22 BAA02g29670 A02 17017650 C T upstream_gene_variant MODIFIER c.-1818G>A| S150
S60
23 BAA02g29670 A02 17017670 C T upstream_gene_variant MODIFIER c.-1838G>A| S274
24 BAA02g29670 A02 17017728 C T upstream_gene_variant MODIFIER c.-1896G>A| S194
25 BAA02g29670 A02 17017826 G A upstream_gene_variant MODIFIER c.-1994C>T| S278