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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g34560 A02 29627339 G A upstream_gene_variant MODIFIER c.-4896G>A| S306
2 BAA02g34560 A02 29627478 C T upstream_gene_variant MODIFIER c.-4757C>T| S9
3 BAA02g34560 A02 29627536 G A upstream_gene_variant MODIFIER c.-4699G>A| S48
4 BAA02g34560 A02 29627895 C T upstream_gene_variant MODIFIER c.-4340C>T| S202
5 BAA02g34560 A02 29628581 G A upstream_gene_variant MODIFIER c.-3654G>A| S203
S69
6 BAA02g34560 A02 29628938 G A upstream_gene_variant MODIFIER c.-3297G>A| S36
7 BAA02g34560 A02 29629911 G A upstream_gene_variant MODIFIER c.-2324G>A| S72
S78
8 BAA02g34560 A02 29630294 C T upstream_gene_variant MODIFIER c.-1941C>T| S189
9 BAA02g34560 A02 29630585 G A upstream_gene_variant MODIFIER c.-1650G>A| S25
10 BAA02g34560 A02 29630657 C T upstream_gene_variant MODIFIER c.-1578C>T| S218
11 BAA02g34560 A02 29630665 G A upstream_gene_variant MODIFIER c.-1570G>A| S186
12 BAA02g34560 A02 29630783 C T upstream_gene_variant MODIFIER c.-1452C>T| S201
13 BAA02g34560 A02 29631436 G A upstream_gene_variant MODIFIER c.-799G>A| S25
14 BAA02g34560 A02 29633055 C T missense_variant MODERATE c.394C>T|p.Leu132Phe S53
15 BAA02g34560 A02 29633780 C T missense_variant MODERATE c.952C>T|p.Pro318Ser S157
S163
16 BAA02g34560 A02 29634741 C T intron_variant MODIFIER c.1647+10C>T| S172
S217
17 BAA02g34560 A02 29636460 G A downstream_gene_variant MODIFIER c.*1049G>A| S8