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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g20960 A05 13156338 G A upstream_gene_variant MODIFIER c.-3440G>A| S159
2 BAA05g20960 A05 13160035 G A missense_variant MODERATE c.163G>A|p.Val55Ile S124
3 BAA05g20960 A05 13160264 C T missense_variant MODERATE c.322C>T|p.Leu108Phe S232
4 BAA05g20960 A05 13160828 G A missense_variant MODERATE c.886G>A|p.Gly296Arg S230
5 BAA05g20960 A05 13161642 C T missense_variant MODERATE c.1288C>T|p.Pro430Ser S305
6 BAA05g20960 A05 13161714 C T missense_variant MODERATE c.1360C>T|p.His454Tyr S83
S88
7 BAA05g20960 A05 13161999 G A missense_variant MODERATE c.1645G>A|p.Val549Ile S66
8 BAA05g20960 A05 13164262 G A synonymous_variant LOW c.1926G>A|p.Arg642Arg S294
9 BAA05g20960 A05 13164574 G A missense_variant MODERATE c.2015G>A|p.Gly672Asp S272
10 BAA05g20960 A05 13166336 G A downstream_gene_variant MODIFIER c.*740G>A| S151
S263
11 BAA05g20960 A05 13166844 C T downstream_gene_variant MODIFIER c.*1248C>T| S202
12 BAA05g20960 A05 13166935 C T downstream_gene_variant MODIFIER c.*1339C>T| S262
13 BAA05g20960 A05 13167300 G A downstream_gene_variant MODIFIER c.*1704G>A| S262