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 BAA02g42960 A02 35669955 C T downstream_gene_variant MODIFIER c.*864G>A| S112
2 BAA02g42960 A02 35671672 C T missense_variant MODERATE c.3001G>A|p.Ala1001Thr S183
S198
3 BAA02g42960 A02 35672734 G A synonymous_variant LOW c.2391C>T|p.Ala797Ala S241
4 BAA02g42960 A02 35673592 G A intron_variant MODIFIER c.2260-727C>T| S146
5 BAA02g42960 A02 35675602 C T intron_variant MODIFIER c.2260-2737G>A| S206
S26
6 BAA02g42960 A02 35676959 C T intron_variant MODIFIER c.2259+1897G>A| S295
7 BAA02g42960 A02 35677218 G A intron_variant MODIFIER c.2259+1638C>T| S265
8 BAA02g42960 A02 35677495 G A intron_variant MODIFIER c.2259+1361C>T| S281
9 BAA02g42960 A02 35677901 C T intron_variant MODIFIER c.2259+955G>A| S1
S90
10 BAA02g42960 A02 35678145 C T intron_variant MODIFIER c.2259+711G>A| S149
11 BAA02g42960 A02 35678826 C T intron_variant MODIFIER c.2259+30G>A| S18
12 BAA02g42960 A02 35680596 G A intron_variant MODIFIER c.997-15C>T| S19
13 BAA02g42960 A02 35681820 G A missense_variant MODERATE c.451C>T|p.Leu151Phe S57
14 BAA02g42960 A02 35681839 G A synonymous_variant LOW c.432C>T|p.Pro144Pro S53
15 BAA02g42960 A02 35682307 C T upstream_gene_variant MODIFIER c.-37G>A| S17
16 BAA02g42960 A02 35683182 G A upstream_gene_variant MODIFIER c.-912C>T| S272
17 BAA02g42960 A02 35683371 G A upstream_gene_variant MODIFIER c.-1101C>T| S281
18 BAA02g42960 A02 35683728 C T upstream_gene_variant MODIFIER c.-1458G>A| S226
19 BAA02g42960 A02 35686463 G A upstream_gene_variant MODIFIER c.-4193C>T| S45
20 BAA02g42960 A02 35686870 C T upstream_gene_variant MODIFIER c.-4600G>A| S87