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 BAA02g39260 A02 33368310 C T upstream_gene_variant MODIFIER c.-4136C>T| S79
S84
2 BAA02g39260 A02 33368695 C T upstream_gene_variant MODIFIER c.-3751C>T| S202
3 BAA02g39260 A02 33370449 G A upstream_gene_variant MODIFIER c.-1997G>A| S192
4 BAA02g39260 A02 33370698 C T upstream_gene_variant MODIFIER c.-1748C>T| S46
5 BAA02g39260 A02 33370797 C T upstream_gene_variant MODIFIER c.-1649C>T| S131
6 BAA02g39260 A02 33370878 G A upstream_gene_variant MODIFIER c.-1568G>A| S297
7 BAA02g39260 A02 33371638 G A upstream_gene_variant MODIFIER c.-808G>A| S148
S210
8 BAA02g39260 A02 33372682 G A synonymous_variant LOW c.237G>A|p.Glu79Glu S278
9 BAA02g39260 A02 33372685 G A synonymous_variant LOW c.240G>A|p.Thr80Thr S172
S217
10 BAA02g39260 A02 33375018 C T intron_variant MODIFIER c.812-18C>T| S250
11 BAA02g39260 A02 33375474 G A intron_variant MODIFIER c.928-253G>A| S247
12 BAA02g39260 A02 33375844 C T missense_variant MODERATE c.1045C>T|p.Leu349Phe S33
13 BAA02g39260 A02 33375996 C T missense_variant MODERATE c.1103C>T|p.Thr368Ile S246
14 BAA02g39260 A02 33376071 C T intron_variant MODIFIER c.1158+20C>T| S53
15 BAA02g39260 A02 33376881 G A missense_variant MODERATE c.1753G>A|p.Glu585Lys S62
16 BAA02g39260 A02 33377298 C T missense_variant MODERATE c.1921C>T|p.Pro641Ser S73
S91
17 BAA02g39260 A02 33377498 C T missense_variant MODERATE c.2048C>T|p.Ala683Val S9
18 BAA02g39260 A02 33381381 G A downstream_gene_variant MODIFIER c.*3774G>A| S13