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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g40130 A09 47436101 G A upstream_gene_variant MODIFIER c.-3185G>A| S162
2 BAA09g40130 A09 47439755 C T missense_variant MODERATE c.250C>T|p.Pro84Ser S1
3 BAA09g40130 A09 47439957 G A missense_variant MODERATE c.371G>A|p.Ser124Asn S93
4 BAA09g40130 A09 47440156 T A stop_gained HIGH c.570T>A|p.Tyr190* S208
S93
5 BAA09g40130 A09 47440168 C T synonymous_variant LOW c.582C>T|p.Cys194Cys S36
6 BAA09g40130 A09 47442547 C T synonymous_variant LOW c.2334C>T|p.Asn778Asn S277
7 BAA09g40130 A09 47442581 C T synonymous_variant LOW c.2368C>T|p.Leu790Leu S293
8 BAA09g40130 A09 47443233 G A missense_variant MODERATE c.2837G>A|p.Arg946Lys S151
S263
9 BAA09g40130 A09 47443696 G A missense_variant MODERATE c.3097G>A|p.Glu1033Lys S176
10 BAA09g40130 A09 47446618 C T missense_variant MODERATE c.5753C>T|p.Ser1918Phe S133
11 BAA09g40130 A09 47446880 G A synonymous_variant LOW c.6015G>A|p.Lys2005Lys S86
12 BAA09g40130 A09 47446888 G A missense_variant MODERATE c.6023G>A|p.Arg2008Gln S34
13 BAA09g40130 A09 47448407 C T downstream_gene_variant MODIFIER c.*1386C>T| S267