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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g23100 A01 11803929 C T upstream_gene_variant MODIFIER c.-1310C>T| S160
2 BAA01g23100 A01 11804344 C T upstream_gene_variant MODIFIER c.-895C>T| S143
3 BAA01g23100 A01 11804360 G A upstream_gene_variant MODIFIER c.-879G>A| S263
4 BAA01g23100 A01 11804459 C T upstream_gene_variant MODIFIER c.-780C>T| S198
5 BAA01g23100 A01 11804676 G A upstream_gene_variant MODIFIER c.-563G>A| S59
6 BAA01g23100 A01 11805321 C T intron_variant MODIFIER c.58+25C>T| S210
7 BAA01g23100 A01 11806185 C T intron_variant MODIFIER c.346+118C>T| S182
8 BAA01g23100 A01 11806262 C T intron_variant MODIFIER c.347-72C>T| S303
9 BAA01g23100 A01 11806319 G A intron_variant MODIFIER c.347-15G>A| S308
10 BAA01g23100 A01 11806525 C T missense_variant MODERATE c.538C>T|p.Pro180Ser S54
11 BAA01g23100 A01 11806542 G A synonymous_variant LOW c.555G>A|p.Glu185Glu S84
S93
12 BAA01g23100 A01 11806943 C T missense_variant MODERATE c.956C>T|p.Ala319Val S242
13 BAA01g23100 A01 11807096 G A missense_variant MODERATE c.1109G>A|p.Gly370Glu S301
S304
14 BAA01g23100 A01 11807602 C T missense_variant MODERATE c.1615C>T|p.Leu539Phe S139
15 BAA01g23100 A01 11809420 C T downstream_gene_variant MODIFIER c.*1126C>T| S167
16 BAA01g23100 A01 11809696 C T downstream_gene_variant MODIFIER c.*1402C>T| S4
17 BAA01g23100 A01 11810076 G A downstream_gene_variant MODIFIER c.*1782G>A| S144
18 BAA01g23100 A01 11810182 C T downstream_gene_variant MODIFIER c.*1888C>T| S168
19 BAA01g23100 A01 11810291 A T downstream_gene_variant MODIFIER c.*1997A>T| S299
20 BAA01g23100 A01 11810535 G A downstream_gene_variant MODIFIER c.*2241G>A| S283
21 BAA01g23100 A01 11810656 G A downstream_gene_variant MODIFIER c.*2362G>A| S240