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 BAA01g17780 A01 8641584 C T downstream_gene_variant MODIFIER c.*4227G>A| S99
2 BAA01g17780 A01 8642483 C T downstream_gene_variant MODIFIER c.*3328G>A| S146
3 BAA01g17780 A01 8643210 C T downstream_gene_variant MODIFIER c.*2601G>A| S70
4 BAA01g17780 A01 8643561 C T downstream_gene_variant MODIFIER c.*2250G>A| S284
5 BAA01g17780 A01 8644011 C T downstream_gene_variant MODIFIER c.*1800G>A| S47
6 BAA01g17780 A01 8644211 C T downstream_gene_variant MODIFIER c.*1600G>A| S88
7 BAA01g17780 A01 8644928 C T downstream_gene_variant MODIFIER c.*883G>A| S179
8 BAA01g17780 A01 8644963 G A downstream_gene_variant MODIFIER c.*848C>T| S195
9 BAA01g17780 A01 8644970 G A downstream_gene_variant MODIFIER c.*841C>T| S262
10 BAA01g17780 A01 8646609 C T missense_variant MODERATE c.721G>A|p.Ala241Thr S40
S49
11 BAA01g17780 A01 8647237 G A missense_variant MODERATE c.490C>T|p.Leu164Phe S178
12 BAA01g17780 A01 8647352 C T synonymous_variant LOW c.375G>A|p.Lys125Lys S88
13 BAA01g17780 A01 8647364 G A synonymous_variant LOW c.363C>T|p.Ile121Ile S94
14 BAA01g17780 A01 8647511 C T missense_variant MODERATE c.292G>A|p.Gly98Arg S51
15 BAA01g17780 A01 8648668 G A upstream_gene_variant MODIFIER c.-866C>T| S84
S93
16 BAA01g17780 A01 8649663 C T upstream_gene_variant MODIFIER c.-1861G>A| S255
17 BAA01g17780 A01 8651533 G A upstream_gene_variant MODIFIER c.-3731C>T| S172
S217