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


Gene ID

Results: 1 - 27 of 27 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g26330 A02 14616318 C T upstream_gene_variant MODIFIER c.-967C>T| S194
2 BAA02g26330 A02 14616923 C T upstream_gene_variant MODIFIER c.-362C>T| S135
3 BAA02g26330 A02 14617357 G A missense_variant MODERATE c.73G>A|p.Glu25Lys S89
4 BAA02g26330 A02 14617807 G A missense_variant MODERATE c.523G>A|p.Gly175Arg S71
5 BAA02g26330 A02 14618059 C T stop_gained HIGH c.775C>T|p.Gln259* S63
6 BAA02g26330 A02 14618263 G A missense_variant MODERATE c.979G>A|p.Glu327Lys S260
7 BAA02g26330 A02 14618454 C T intron_variant MODIFIER c.1144+26C>T| S9
8 BAA02g26330 A02 14618652 C T intron_variant MODIFIER c.1144+224C>T| S250
9 BAA02g26330 A02 14619230 C T missense_variant MODERATE c.1244C>T|p.Ala415Val S33
10 BAA02g26330 A02 14619340 G A missense_variant MODERATE c.1354G>A|p.Asp452Asn S23
11 BAA02g26330 A02 14620141 G A intron_variant MODIFIER c.1977+14G>A| S279
12 BAA02g26330 A02 14620428 G A intron_variant MODIFIER c.2035+78G>A| S100
S251
13 BAA02g26330 A02 14620482 C A intron_variant MODIFIER c.2036-81C>A| S172
S217
14 BAA02g26330 A02 14622432 G A splice_region_variant&intron_variant LOW c.3291+6G>A| S150
15 BAA02g26330 A02 14622462 G A intron_variant MODIFIER c.3291+36G>A| S228
16 BAA02g26330 A02 14623360 G A missense_variant MODERATE c.3887G>A|p.Ser1296Asn S191
17 BAA02g26330 A02 14624732 G A downstream_gene_variant MODIFIER c.*1045G>A| S61
18 BAA02g26330 A02 14624738 G A downstream_gene_variant MODIFIER c.*1051G>A| S223
19 BAA02g26330 A02 14625911 G A downstream_gene_variant MODIFIER c.*2224G>A| S132
S137
S215
S89
20 BAA02g26330 A02 14626312 G A downstream_gene_variant MODIFIER c.*2625G>A| S146
21 BAA02g26330 A02 14626335 C T downstream_gene_variant MODIFIER c.*2648C>T| S296
22 BAA02g26330 A02 14626804 G A downstream_gene_variant MODIFIER c.*3117G>A| S269
23 BAA02g26330 A02 14627486 C T downstream_gene_variant MODIFIER c.*3799C>T| S177
24 BAA02g26330 A02 14627536 C T downstream_gene_variant MODIFIER c.*3849C>T| S33
25 BAA02g26330 A02 14627858 C T downstream_gene_variant MODIFIER c.*4171C>T| S274