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 BAA01g32700 A01 21661248 C T upstream_gene_variant MODIFIER c.-3154C>T| S205
2 BAA01g32700 A01 21661256 C T upstream_gene_variant MODIFIER c.-3146C>T| S28
3 BAA01g32700 A01 21661463 G A upstream_gene_variant MODIFIER c.-2939G>A| S221
4 BAA01g32700 A01 21661975 G A upstream_gene_variant MODIFIER c.-2427G>A| S308
5 BAA01g32700 A01 21662921 G A upstream_gene_variant MODIFIER c.-1481G>A| S176
6 BAA01g32700 A01 21663461 C T upstream_gene_variant MODIFIER c.-941C>T| S64
7 BAA01g32700 A01 21664466 G A missense_variant MODERATE c.65G>A|p.Arg22His S129
8 BAA01g32700 A01 21665451 G A synonymous_variant LOW c.1050G>A|p.Ser350Ser S197
9 BAA01g32700 A01 21665557 G A missense_variant MODERATE c.1156G>A|p.Gly386Arg S263
10 BAA01g32700 A01 21665570 C T missense_variant MODERATE c.1169C>T|p.Ser390Leu S120
11 BAA01g32700 A01 21665616 A G intron_variant MODIFIER c.1192+23A>G| S128
12 BAA01g32700 A01 21666276 C T intron_variant MODIFIER c.1193-181C>T| S251
13 BAA01g32700 A01 21666464 C T synonymous_variant LOW c.1200C>T|p.Val400Val S39
14 BAA01g32700 A01 21667633 G A intron_variant MODIFIER c.1659+710G>A| S292
15 BAA01g32700 A01 21667853 C T intron_variant MODIFIER c.1660-547C>T| S82
S92
16 BAA01g32700 A01 21669110 C T synonymous_variant LOW c.2115C>T|p.Ile705Ile S18
17 BAA01g32700 A01 21673423 G A downstream_gene_variant MODIFIER c.*3662G>A| S173
18 BAA01g32700 A01 21674485 C T downstream_gene_variant MODIFIER c.*4724C>T| S40
S49