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 BAA09g11220 A09 6308150 C T upstream_gene_variant MODIFIER c.-2165C>T| S26
2 BAA09g11220 A09 6308328 C T upstream_gene_variant MODIFIER c.-1987C>T| S5
3 BAA09g11220 A09 6308382 C T upstream_gene_variant MODIFIER c.-1933C>T| S292
4 BAA09g11220 A09 6308582 G A upstream_gene_variant MODIFIER c.-1733G>A| S296
5 BAA09g11220 A09 6308735 G A upstream_gene_variant MODIFIER c.-1580G>A| S200
6 BAA09g11220 A09 6308826 G A upstream_gene_variant MODIFIER c.-1489G>A| S163
7 BAA09g11220 A09 6309204 G A upstream_gene_variant MODIFIER c.-1111G>A| S299
8 BAA09g11220 A09 6310560 C T synonymous_variant LOW c.246C>T|p.Asp82Asp S217
S248
9 BAA09g11220 A09 6310608 G A synonymous_variant LOW c.294G>A|p.Ser98Ser S236
S286
S79
10 BAA09g11220 A09 6310764 C T synonymous_variant LOW c.450C>T|p.Val150Val S270
11 BAA09g11220 A09 6311037 G A synonymous_variant LOW c.723G>A|p.Gly241Gly S210
12 BAA09g11220 A09 6311197 G A missense_variant MODERATE c.883G>A|p.Asp295Asn S219
S72
13 BAA09g11220 A09 6311270 G A missense_variant MODERATE c.956G>A|p.Ser319Asn S189
14 BAA09g11220 A09 6311443 G A missense_variant MODERATE c.1129G>A|p.Glu377Lys S79
S91
15 BAA09g11220 A09 6311492 C T missense_variant MODERATE c.1178C>T|p.Ser393Phe S294
16 BAA09g11220 A09 6311706 C T downstream_gene_variant MODIFIER c.*21C>T| S292
17 BAA09g11220 A09 6313055 A T downstream_gene_variant MODIFIER c.*1370A>T| S27
18 BAA09g11220 A09 6313072 C T downstream_gene_variant MODIFIER c.*1387C>T| S273
19 BAA09g11220 A09 6313139 G A downstream_gene_variant MODIFIER c.*1454G>A| S223
20 BAA09g11220 A09 6314153 G A downstream_gene_variant MODIFIER c.*2468G>A| S169
21 BAA09g11220 A09 6314206 G A downstream_gene_variant MODIFIER c.*2521G>A| S78
22 BAA09g11220 A09 6314758 G A downstream_gene_variant MODIFIER c.*3073G>A| S152
S185
S273
S68
23 BAA09g11220 A09 6315814 C T downstream_gene_variant MODIFIER c.*4129C>T| S136
24 BAA09g11220 A09 6316053 G A downstream_gene_variant MODIFIER c.*4368G>A| S188
25 BAA09g11220 A09 6316292 G A downstream_gene_variant MODIFIER c.*4607G>A| S112