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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g14980 A05 7993358 G A downstream_gene_variant MODIFIER c.*2731C>T| S240
2 BAA05g14980 A05 7996255 G A missense_variant MODERATE c.2654C>T|p.Thr885Met S293
3 BAA05g14980 A05 7996449 C T synonymous_variant LOW c.2460G>A|p.Glu820Glu S169
4 BAA05g14980 A05 7996460 C T missense_variant MODERATE c.2449G>A|p.Ala817Thr S15
5 BAA05g14980 A05 7996981 G A missense_variant MODERATE c.1928C>T|p.Ala643Val S70
6 BAA05g14980 A05 7997500 C T stop_gained HIGH c.1409G>A|p.Trp470* S8
7 BAA05g14980 A05 7997841 G A missense_variant MODERATE c.1153C>T|p.Pro385Ser S187
S245
8 BAA05g14980 A05 7998464 C T missense_variant MODERATE c.1115G>A|p.Gly372Glu S58
9 BAA05g14980 A05 7998517 C T synonymous_variant LOW c.1062G>A|p.Thr354Thr S171
10 BAA05g14980 A05 7998638 G A missense_variant MODERATE c.941C>T|p.Thr314Ile S144
11 BAA05g14980 A05 7998885 G A missense_variant MODERATE c.694C>T|p.Arg232Trp S210
12 BAA05g14980 A05 7998925 G A synonymous_variant LOW c.654C>T|p.Asp218Asp S238
13 BAA05g14980 A05 7999501 G A synonymous_variant LOW c.78C>T|p.Val26Val S284
14 BAA05g14980 A05 8000013 C T upstream_gene_variant MODIFIER c.-435G>A| S191
15 BAA05g14980 A05 8000287 G A upstream_gene_variant MODIFIER c.-709C>T| S134
16 BAA05g14980 A05 8002991 C T upstream_gene_variant MODIFIER c.-3413G>A| S169
17 BAA05g14980 A05 8003105 C T upstream_gene_variant MODIFIER c.-3527G>A| S143
18 BAA05g14980 A05 8003870 C T upstream_gene_variant MODIFIER c.-4292G>A| S140
19 BAA05g14980 A05 8004172 G A upstream_gene_variant MODIFIER c.-4594C>T| S47
20 BAA05g14980 A05 8004385 G A upstream_gene_variant MODIFIER c.-4807C>T| S34