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 BAA05g19060 A05 11119619 G A downstream_gene_variant MODIFIER c.*4656C>T| S23
2 BAA05g19060 A05 11119666 G A downstream_gene_variant MODIFIER c.*4609C>T| S129
3 BAA05g19060 A05 11120062 G A downstream_gene_variant MODIFIER c.*4213C>T| S293
4 BAA05g19060 A05 11120063 A G downstream_gene_variant MODIFIER c.*4212T>C| S238
5 BAA05g19060 A05 11120370 G A downstream_gene_variant MODIFIER c.*3905C>T| S148
S210
6 BAA05g19060 A05 11120710 C T downstream_gene_variant MODIFIER c.*3565G>A| S164
7 BAA05g19060 A05 11121338 C T downstream_gene_variant MODIFIER c.*2937G>A| S71
8 BAA05g19060 A05 11121937 G A downstream_gene_variant MODIFIER c.*2338C>T| S122
9 BAA05g19060 A05 11122353 C T downstream_gene_variant MODIFIER c.*1922G>A| S116
10 BAA05g19060 A05 11122770 G A downstream_gene_variant MODIFIER c.*1505C>T| S109
11 BAA05g19060 A05 11123399 C T downstream_gene_variant MODIFIER c.*876G>A| S15
12 BAA05g19060 A05 11124335 C T synonymous_variant LOW c.561G>A|p.Lys187Lys S81
S85
13 BAA05g19060 A05 11124474 G A missense_variant MODERATE c.422C>T|p.Ser141Phe S40
S49
14 BAA05g19060 A05 11124657 C T missense_variant MODERATE c.239G>A|p.Arg80His S130
15 BAA05g19060 A05 11126696 G A upstream_gene_variant MODIFIER c.-1801C>T| S11
16 BAA05g19060 A05 11126822 C T upstream_gene_variant MODIFIER c.-1927G>A| S43
17 BAA05g19060 A05 11127985 G A upstream_gene_variant MODIFIER c.-3090C>T| S265
S296
18 BAA05g19060 A05 11128750 C T upstream_gene_variant MODIFIER c.-3855G>A| S295
19 BAA05g19060 A05 11129065 G A upstream_gene_variant MODIFIER c.-4170C>T| S158