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 BAA08g12990 A08 11290632 G A upstream_gene_variant MODIFIER c.-4391G>A| S294
2 BAA08g12990 A08 11290722 C T upstream_gene_variant MODIFIER c.-4301C>T| S160
3 BAA08g12990 A08 11291191 G A upstream_gene_variant MODIFIER c.-3832G>A| S274
4 BAA08g12990 A08 11291378 C T upstream_gene_variant MODIFIER c.-3645C>T| S226
5 BAA08g12990 A08 11291529 C T upstream_gene_variant MODIFIER c.-3494C>T| S132
S137
S138
S215
S237
S288
6 BAA08g12990 A08 11291550 C T upstream_gene_variant MODIFIER c.-3473C>T| S50
7 BAA08g12990 A08 11291653 C T upstream_gene_variant MODIFIER c.-3370C>T| S207
8 BAA08g12990 A08 11291715 C T upstream_gene_variant MODIFIER c.-3308C>T| S15
S156
S3
S34
S6
9 BAA08g12990 A08 11291768 G A upstream_gene_variant MODIFIER c.-3255G>A| S33
10 BAA08g12990 A08 11293564 C T upstream_gene_variant MODIFIER c.-1459C>T| S152
11 BAA08g12990 A08 11293962 G A upstream_gene_variant MODIFIER c.-1061G>A| S180
12 BAA08g12990 A08 11294151 C T upstream_gene_variant MODIFIER c.-872C>T| S230
13 BAA08g12990 A08 11294557 C T upstream_gene_variant MODIFIER c.-466C>T| S15
S3
14 BAA08g12990 A08 11295398 C T missense_variant MODERATE c.281C>T|p.Ala94Val S47
15 BAA08g12990 A08 11295822 C T synonymous_variant LOW c.510C>T|p.Ile170Ile S262
16 BAA08g12990 A08 11296833 G A missense_variant MODERATE c.1150G>A|p.Asp384Asn S281
17 BAA08g12990 A08 11298591 C T downstream_gene_variant MODIFIER c.*499C>T| S82
S92
18 BAA08g12990 A08 11299003 C T downstream_gene_variant MODIFIER c.*911C>T| S256