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 BAA01g07370 A01 3257462 G A upstream_gene_variant MODIFIER c.-4465G>A| S298
2 BAA01g07370 A01 3258050 C T upstream_gene_variant MODIFIER c.-3877C>T| S244
3 BAA01g07370 A01 3258506 C T upstream_gene_variant MODIFIER c.-3421C>T| S150
4 BAA01g07370 A01 3260147 C T upstream_gene_variant MODIFIER c.-1780C>T| S282
5 BAA01g07370 A01 3260184 G A upstream_gene_variant MODIFIER c.-1743G>A| S12
6 BAA01g07370 A01 3260323 G A upstream_gene_variant MODIFIER c.-1604G>A| S103
7 BAA01g07370 A01 3261222 C T upstream_gene_variant MODIFIER c.-705C>T| S133
8 BAA01g07370 A01 3261421 C T upstream_gene_variant MODIFIER c.-506C>T| S45
9 BAA01g07370 A01 3261737 G A upstream_gene_variant MODIFIER c.-190G>A| S170
10 BAA01g07370 A01 3262304 C T synonymous_variant LOW c.378C>T|p.Leu126Leu S18
11 BAA01g07370 A01 3262825 G A missense_variant MODERATE c.542G>A|p.Gly181Asp S79
S91
12 BAA01g07370 A01 3263043 C T missense_variant MODERATE c.760C>T|p.Leu254Phe S61
13 BAA01g07370 A01 3263222 G A synonymous_variant LOW c.939G>A|p.Ser313Ser S45
14 BAA01g07370 A01 3263376 C T intron_variant MODIFIER c.976+117C>T| S20
15 BAA01g07370 A01 3263544 C T intron_variant MODIFIER c.976+285C>T| S296
16 BAA01g07370 A01 3264442 C T downstream_gene_variant MODIFIER c.*353C>T| S250
17 BAA01g07370 A01 3265141 G A downstream_gene_variant MODIFIER c.*1052G>A| S17