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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g33590 A02 28740127 C T downstream_gene_variant MODIFIER c.*3997G>A| S107
2 BAA02g33590 A02 28741092 G A downstream_gene_variant MODIFIER c.*3032C>T| S207
3 BAA02g33590 A02 28741170 G A downstream_gene_variant MODIFIER c.*2954C>T| S126
4 BAA02g33590 A02 28741421 G A downstream_gene_variant MODIFIER c.*2703C>T| S133
5 BAA02g33590 A02 28741573 G A downstream_gene_variant MODIFIER c.*2551C>T| S47
6 BAA02g33590 A02 28744302 C T missense_variant MODERATE c.2030G>A|p.Arg677Lys S84
S93
7 BAA02g33590 A02 28744769 G A synonymous_variant LOW c.1563C>T|p.Asn521Asn S240
8 BAA02g33590 A02 28745093 C T missense_variant MODERATE c.1337G>A|p.Arg446Lys S38
9 BAA02g33590 A02 28745258 C T missense_variant MODERATE c.1172G>A|p.Gly391Glu S149
10 BAA02g33590 A02 28745419 C T synonymous_variant LOW c.1011G>A|p.Glu337Glu S277
11 BAA02g33590 A02 28745487 G A missense_variant MODERATE c.943C>T|p.Leu315Phe S129
12 BAA02g33590 A02 28745600 G A missense_variant MODERATE c.830C>T|p.Ser277Phe S268
13 BAA02g33590 A02 28745608 G A synonymous_variant LOW c.822C>T|p.Arg274Arg S223
14 BAA02g33590 A02 28745642 G A missense_variant MODERATE c.788C>T|p.Ala263Val S35
15 BAA02g33590 A02 28745664 G A missense_variant MODERATE c.766C>T|p.His256Tyr S74
16 BAA02g33590 A02 28745681 C T missense_variant MODERATE c.749G>A|p.Arg250His S295
17 BAA02g33590 A02 28745899 G A synonymous_variant LOW c.531C>T|p.Asp177Asp S69
18 BAA02g33590 A02 28746132 C T synonymous_variant LOW c.375G>A|p.Lys125Lys S15
S3
19 BAA02g33590 A02 28746566 G A missense_variant MODERATE c.55C>T|p.Arg19Trp S279
20 BAA02g33590 A02 28746596 C T missense_variant MODERATE c.25G>A|p.Glu9Lys S241
21 BAA02g33590 A02 28746822 C T upstream_gene_variant MODIFIER c.-202G>A| S212
22 BAA02g33590 A02 28746829 C T upstream_gene_variant MODIFIER c.-209G>A| S164
23 BAA02g33590 A02 28748236 G A upstream_gene_variant MODIFIER c.-1616C>T| S278
24 BAA02g33590 A02 28749414 G A upstream_gene_variant MODIFIER c.-2794C>T| S5
25 BAA02g33590 A02 28750414 C T upstream_gene_variant MODIFIER c.-3794G>A| S38