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 BAA06g32820 A06 22200064 C T upstream_gene_variant MODIFIER c.-4987C>T| S46
2 BAA06g32820 A06 22205286 G A stop_gained HIGH c.236G>A|p.Trp79* S213
3 BAA06g32820 A06 22206691 G T missense_variant MODERATE c.848G>T|p.Gly283Val S100
4 BAA06g32820 A06 22207759 G A missense_variant MODERATE c.1367G>A|p.Arg456Lys S110
5 BAA06g32820 A06 22208565 G A synonymous_variant LOW c.1782G>A|p.Lys594Lys S226
6 BAA06g32820 A06 22208999 C T intron_variant MODIFIER c.2019+22C>T| S18
7 BAA06g32820 A06 22209229 C T intron_variant MODIFIER c.2137-33C>T| S302
8 BAA06g32820 A06 22209398 G A missense_variant MODERATE c.2273G>A|p.Gly758Asp S187
9 BAA06g32820 A06 22209529 C T missense_variant MODERATE c.2404C>T|p.Leu802Phe S295
10 BAA06g32820 A06 22209756 C T synonymous_variant LOW c.2553C>T|p.Thr851Thr S288
11 BAA06g32820 A06 22211299 C T synonymous_variant LOW c.3429C>T|p.Phe1143Phe S127
12 BAA06g32820 A06 22211985 G A missense_variant MODERATE c.3835G>A|p.Glu1279Lys S129
13 BAA06g32820 A06 22212867 C T intron_variant MODIFIER c.4526+39C>T| S274
14 BAA06g32820 A06 22214069 G A downstream_gene_variant MODIFIER c.*918G>A| S188
15 BAA06g32820 A06 22215119 G A downstream_gene_variant MODIFIER c.*1968G>A| S146