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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g26960 A02 15104068 C T synonymous_variant LOW c.4779G>A|p.Arg1593Arg S181
2 BAA02g26960 A02 15104140 C T splice_region_variant&synonymous_variant LOW c.4707G>A|p.Leu1569Leu S16
3 BAA02g26960 A02 15104379 G A synonymous_variant LOW c.4557C>T|p.Arg1519Arg S294
4 BAA02g26960 A02 15105542 G A synonymous_variant LOW c.3909C>T|p.Phe1303Phe S161
5 BAA02g26960 A02 15106986 C T missense_variant MODERATE c.2806G>A|p.Glu936Lys S131
6 BAA02g26960 A02 15107174 G A synonymous_variant LOW c.2712C>T|p.Leu904Leu S169
7 BAA02g26960 A02 15107448 G A missense_variant MODERATE c.2438C>T|p.Ser813Phe S173
8 BAA02g26960 A02 15107643 G A missense_variant MODERATE c.2243C>T|p.Pro748Leu S80
9 BAA02g26960 A02 15108595 G A missense_variant MODERATE c.1291C>T|p.His431Tyr S59
10 BAA02g26960 A02 15109298 G A missense_variant MODERATE c.805C>T|p.Pro269Ser S228
11 BAA02g26960 A02 15109348 G A missense_variant MODERATE c.755C>T|p.Ser252Phe S235
12 BAA02g26960 A02 15109398 C T synonymous_variant LOW c.705G>A|p.Gln235Gln S144
13 BAA02g26960 A02 15109737 G A missense_variant MODERATE c.445C>T|p.Pro149Ser S303
14 BAA02g26960 A02 15110708 C T upstream_gene_variant MODIFIER c.-335G>A| S115
15 BAA02g26960 A02 15111134 C T upstream_gene_variant MODIFIER c.-761G>A| S280
16 BAA02g26960 A02 15112980 C T upstream_gene_variant MODIFIER c.-2607G>A| S301
S304
17 BAA02g26960 A02 15114445 C T upstream_gene_variant MODIFIER c.-4072G>A| S42
18 BAA02g26960 A02 15114897 G A upstream_gene_variant MODIFIER c.-4524C>T| S35
19 BAA02g26960 A02 15115241 G A upstream_gene_variant MODIFIER c.-4868C>T| S92
20 BAA02g26960 A02 15115248 C T upstream_gene_variant MODIFIER c.-4875G>A| S284