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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g38670 A09 46422536 C T upstream_gene_variant MODIFIER c.-4760C>T| S306
2 BAA09g38670 A09 46423452 C T upstream_gene_variant MODIFIER c.-3844C>T| S139
3 BAA09g38670 A09 46424241 C T upstream_gene_variant MODIFIER c.-3055C>T| S174
4 BAA09g38670 A09 46424525 C T upstream_gene_variant MODIFIER c.-2771C>T| S144
5 BAA09g38670 A09 46424609 C T upstream_gene_variant MODIFIER c.-2687C>T| S204
6 BAA09g38670 A09 46424666 C T upstream_gene_variant MODIFIER c.-2630C>T| S143
7 BAA09g38670 A09 46424701 G A upstream_gene_variant MODIFIER c.-2595G>A| S207
8 BAA09g38670 A09 46425215 G A upstream_gene_variant MODIFIER c.-2081G>A| S111
9 BAA09g38670 A09 46425223 G A upstream_gene_variant MODIFIER c.-2073G>A| S217
S248
10 BAA09g38670 A09 46426119 C T upstream_gene_variant MODIFIER c.-1177C>T| S293
11 BAA09g38670 A09 46427189 C T upstream_gene_variant MODIFIER c.-107C>T| S174
S27
12 BAA09g38670 A09 46427598 C A intron_variant MODIFIER c.178-37C>A| S198
13 BAA09g38670 A09 46427599 A T intron_variant MODIFIER c.178-36A>T| S198
14 BAA09g38670 A09 46428439 G A synonymous_variant LOW c.648G>A|p.Glu216Glu S151
S263
15 BAA09g38670 A09 46428624 C T missense_variant MODERATE c.748C>T|p.Pro250Ser S191
16 BAA09g38670 A09 46429442 C T downstream_gene_variant MODIFIER c.*89C>T| S251