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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g29790 A08 20350076 C T synonymous_variant LOW c.2574G>A|p.Glu858Glu S25
2 BAA08g29790 A08 20352237 G A synonymous_variant LOW c.1071C>T|p.Asp357Asp S188
3 BAA08g29790 A08 20352862 C T missense_variant MODERATE c.724G>A|p.Glu242Lys S83
S88
4 BAA08g29790 A08 20354293 C T intron_variant MODIFIER c.673-1380G>A| S176
5 BAA08g29790 A08 20354956 C T intron_variant MODIFIER c.672+1675G>A| S174
6 BAA08g29790 A08 20355322 C T intron_variant MODIFIER c.672+1309G>A| S212
S288
7 BAA08g29790 A08 20355325 C T intron_variant MODIFIER c.672+1306G>A| S223
8 BAA08g29790 A08 20355418 C T intron_variant MODIFIER c.672+1213G>A| S206
S26
9 BAA08g29790 A08 20356139 C T intron_variant MODIFIER c.672+492G>A| S39
10 BAA08g29790 A08 20357359 G A missense_variant MODERATE c.73C>T|p.His25Tyr S65
11 BAA08g29790 A08 20357524 G A upstream_gene_variant MODIFIER c.-93C>T| S204
12 BAA08g29790 A08 20358316 C T upstream_gene_variant MODIFIER c.-885G>A| S210
13 BAA08g29790 A08 20358436 G A upstream_gene_variant MODIFIER c.-1005C>T| S79
S91
14 BAA08g29790 A08 20358448 C T upstream_gene_variant MODIFIER c.-1017G>A| S298
15 BAA08g29790 A08 20358996 G A upstream_gene_variant MODIFIER c.-1565C>T| S136
16 BAA08g29790 A08 20359629 G A upstream_gene_variant MODIFIER c.-2198C>T| S122
17 BAA08g29790 A08 20362082 C T upstream_gene_variant MODIFIER c.-4651G>A| S168