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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g15490 A08 13060092 G A downstream_gene_variant MODIFIER c.*3695C>T| S224
2 BAA08g15490 A08 13060546 C T downstream_gene_variant MODIFIER c.*3241G>A| S163
3 BAA08g15490 A08 13060595 C T downstream_gene_variant MODIFIER c.*3192G>A| S46
4 BAA08g15490 A08 13060640 G T downstream_gene_variant MODIFIER c.*3147C>A| S132
S137
5 BAA08g15490 A08 13060717 G A downstream_gene_variant MODIFIER c.*3070C>T| S238
6 BAA08g15490 A08 13060967 C T downstream_gene_variant MODIFIER c.*2820G>A| S142
7 BAA08g15490 A08 13061083 C T downstream_gene_variant MODIFIER c.*2704G>A| S206
S26
8 BAA08g15490 A08 13061366 G A downstream_gene_variant MODIFIER c.*2421C>T| S87
9 BAA08g15490 A08 13062595 C T downstream_gene_variant MODIFIER c.*1192G>A| S157
S163
10 BAA08g15490 A08 13062728 C T downstream_gene_variant MODIFIER c.*1059G>A| S9
11 BAA08g15490 A08 13063152 G A downstream_gene_variant MODIFIER c.*635C>T| S192
12 BAA08g15490 A08 13063153 G A downstream_gene_variant MODIFIER c.*634C>T| S182
13 BAA08g15490 A08 13065144 C T missense_variant MODERATE c.50G>A|p.Gly17Glu S216
14 BAA08g15490 A08 13069034 C T upstream_gene_variant MODIFIER c.-3841G>A| S236
15 BAA08g15490 A08 13069060 C T upstream_gene_variant MODIFIER c.-3867G>A| S247