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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g04820 A07 4016723 C T downstream_gene_variant MODIFIER c.*4184G>A| S45
2 BAA07g04820 A07 4018834 C T downstream_gene_variant MODIFIER c.*2073G>A| S99
3 BAA07g04820 A07 4018886 C T downstream_gene_variant MODIFIER c.*2021G>A| S142
4 BAA07g04820 A07 4018986 C T downstream_gene_variant MODIFIER c.*1921G>A| S270
5 BAA07g04820 A07 4019192 C T downstream_gene_variant MODIFIER c.*1715G>A| S100
6 BAA07g04820 A07 4019401 C T downstream_gene_variant MODIFIER c.*1506G>A| S11
7 BAA07g04820 A07 4019860 C T downstream_gene_variant MODIFIER c.*1047G>A| S18
8 BAA07g04820 A07 4020039 C T downstream_gene_variant MODIFIER c.*868G>A| S18
9 BAA07g04820 A07 4020054 G A downstream_gene_variant MODIFIER c.*853C>T| S25
10 BAA07g04820 A07 4020067 G A downstream_gene_variant MODIFIER c.*840C>T| S233
11 BAA07g04820 A07 4020148 G A downstream_gene_variant MODIFIER c.*759C>T| S202
12 BAA07g04820 A07 4020548 C T downstream_gene_variant MODIFIER c.*359G>A| S267
13 BAA07g04820 A07 4020745 G A downstream_gene_variant MODIFIER c.*162C>T| S288
14 BAA07g04820 A07 4021091 G A intron_variant MODIFIER c.1299+35C>T| S283
15 BAA07g04820 A07 4021327 C T synonymous_variant LOW c.1098G>A|p.Gly366Gly S35
16 BAA07g04820 A07 4022646 C T intron_variant MODIFIER c.410-24G>A| S294
17 BAA07g04820 A07 4023084 C T missense_variant MODERATE c.121G>A|p.Glu41Lys S240
18 BAA07g04820 A07 4025640 G A upstream_gene_variant MODIFIER c.-2436C>T| S119