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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g13450 A02 6174407 G A upstream_gene_variant MODIFIER c.-3211G>A| S28
2 BAA02g13450 A02 6174482 G A upstream_gene_variant MODIFIER c.-3136G>A| S110
3 BAA02g13450 A02 6175821 G A upstream_gene_variant MODIFIER c.-1797G>A| S161
4 BAA02g13450 A02 6176495 G A upstream_gene_variant MODIFIER c.-1123G>A| S295
5 BAA02g13450 A02 6176692 C T upstream_gene_variant MODIFIER c.-926C>T| S192
6 BAA02g13450 A02 6177350 G A upstream_gene_variant MODIFIER c.-268G>A| S45
7 BAA02g13450 A02 6177851 G A missense_variant MODERATE c.148G>A|p.Ala50Thr S193
8 BAA02g13450 A02 6178128 C T intron_variant MODIFIER c.298+21C>T| S172
S217
9 BAA02g13450 A02 6178505 G A missense_variant MODERATE c.538G>A|p.Gly180Arg S48
10 BAA02g13450 A02 6178735 C T intron_variant MODIFIER c.636+39C>T| S152
11 BAA02g13450 A02 6179541 C T intron_variant MODIFIER c.1014+57C>T| S185
12 BAA02g13450 A02 6179952 G A splice_acceptor_variant&intron_variant HIGH c.1182-1G>A| S239
13 BAA02g13450 A02 6179977 C T synonymous_variant LOW c.1206C>T|p.Asp402Asp S283
14 BAA02g13450 A02 6180101 G A intron_variant MODIFIER c.1290+40G>A| S166
15 BAA02g13450 A02 6180228 C T intron_variant MODIFIER c.1346+16C>T| S186
16 BAA02g13450 A02 6180630 G A intron_variant MODIFIER c.1473+48G>A| S167
S236
S262
S263
17 BAA02g13450 A02 6180906 C T intron_variant MODIFIER c.1600-27C>T| S165
18 BAA02g13450 A02 6182344 G A missense_variant MODERATE c.2255G>A|p.Ser752Asn S298
19 BAA02g13450 A02 6182775 G A missense_variant MODERATE c.2422G>A|p.Glu808Lys S60
20 BAA02g13450 A02 6184064 C T missense_variant MODERATE c.3137C>T|p.Pro1046Leu S167
21 BAA02g13450 A02 6185891 C T downstream_gene_variant MODIFIER c.*1644C>T| S115
22 BAA02g13450 A02 6186494 C T downstream_gene_variant MODIFIER c.*2247C>T| S292