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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g43400 A02 35953800 G A upstream_gene_variant MODIFIER c.-4341G>A| S232
2 BAA02g43400 A02 35954032 C T upstream_gene_variant MODIFIER c.-4109C>T| S124
3 BAA02g43400 A02 35954504 G A upstream_gene_variant MODIFIER c.-3637G>A| S238
4 BAA02g43400 A02 35954528 G A upstream_gene_variant MODIFIER c.-3613G>A| S125
5 BAA02g43400 A02 35956562 C T upstream_gene_variant MODIFIER c.-1579C>T| S179
6 BAA02g43400 A02 35956617 G A upstream_gene_variant MODIFIER c.-1524G>A| S25
7 BAA02g43400 A02 35956733 C T upstream_gene_variant MODIFIER c.-1408C>T| S158
8 BAA02g43400 A02 35956882 C T upstream_gene_variant MODIFIER c.-1259C>T| S119
9 BAA02g43400 A02 35957319 G A upstream_gene_variant MODIFIER c.-822G>A| S56
10 BAA02g43400 A02 35957610 C T upstream_gene_variant MODIFIER c.-531C>T| S295
11 BAA02g43400 A02 35958386 C T stop_gained HIGH c.169C>T|p.Arg57* S296
12 BAA02g43400 A02 35959102 C T missense_variant MODERATE c.385C>T|p.Leu129Phe S240
13 BAA02g43400 A02 35959807 C T synonymous_variant LOW c.690C>T|p.Ala230Ala S206
S26
14 BAA02g43400 A02 35960107 G A synonymous_variant LOW c.990G>A|p.Glu330Glu S161
15 BAA02g43400 A02 35960301 C T missense_variant MODERATE c.1184C>T|p.Pro395Leu S133
S48
16 BAA02g43400 A02 35960564 G A missense_variant MODERATE c.1447G>A|p.Ala483Thr S265
17 BAA02g43400 A02 35961569 G A missense_variant MODERATE c.1918G>A|p.Asp640Asn S268
18 BAA02g43400 A02 35961705 C T missense_variant MODERATE c.1978C>T|p.Pro660Ser S233