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


Gene ID

Results: 1 - 32 of 32 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g35880 A05 36294047 G A upstream_gene_variant MODIFIER c.-3808G>A| S163
2 BAA05g35880 A05 36294631 C T upstream_gene_variant MODIFIER c.-3224C>T| S83
S88
3 BAA05g35880 A05 36294721 G A upstream_gene_variant MODIFIER c.-3134G>A| S217
4 BAA05g35880 A05 36295347 C T upstream_gene_variant MODIFIER c.-2508C>T| S32
5 BAA05g35880 A05 36296176 C T upstream_gene_variant MODIFIER c.-1679C>T| S269
6 BAA05g35880 A05 36296334 C T upstream_gene_variant MODIFIER c.-1521C>T| S8
7 BAA05g35880 A05 36298463 G A intron_variant MODIFIER c.250+115G>A| S295
8 BAA05g35880 A05 36298641 C T intron_variant MODIFIER c.251-115C>T| S133
9 BAA05g35880 A05 36299299 C T intron_variant MODIFIER c.546+50C>T| S233
10 BAA05g35880 A05 36299457 G A intron_variant MODIFIER c.645+10G>A| S143
11 BAA05g35880 A05 36299588 C T missense_variant MODERATE c.704C>T|p.Ala235Val S165
12 BAA05g35880 A05 36300055 C T synonymous_variant LOW c.984C>T|p.Phe328Phe S208
S93
13 BAA05g35880 A05 36300504 G A synonymous_variant LOW c.1209G>A|p.Gly403Gly S224
14 BAA05g35880 A05 36301474 C T intron_variant MODIFIER c.1708-29C>T| S152
15 BAA05g35880 A05 36301749 C T synonymous_variant LOW c.1869C>T|p.Asp623Asp S289
S290
16 BAA05g35880 A05 36302084 G A missense_variant MODERATE c.2034G>A|p.Met678Ile S160
17 BAA05g35880 A05 36302450 G A missense_variant MODERATE c.2239G>A|p.Glu747Lys S295
18 BAA05g35880 A05 36302453 G A missense_variant MODERATE c.2242G>A|p.Ala748Thr S153
19 BAA05g35880 A05 36302794 G A missense_variant MODERATE c.2491G>A|p.Gly831Arg S239
20 BAA05g35880 A05 36303745 C T stop_gained HIGH c.3280C>T|p.Gln1094* S132
S137
S215
21 BAA05g35880 A05 36304548 C T missense_variant MODERATE c.3995C>T|p.Thr1332Ile S297
22 BAA05g35880 A05 36304749 C T missense_variant MODERATE c.4196C>T|p.Ala1399Val S148
23 BAA05g35880 A05 36306213 G A downstream_gene_variant MODIFIER c.*44G>A| S192
24 BAA05g35880 A05 36306432 C T downstream_gene_variant MODIFIER c.*263C>T| S144
25 BAA05g35880 A05 36306540 C T downstream_gene_variant MODIFIER c.*371C>T| S71