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


Gene ID

Results: 1 - 30 of 30 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g42970 A02 35698977 G A upstream_gene_variant MODIFIER c.-3724G>A| S268
2 BAA02g42970 A02 35700768 C T upstream_gene_variant MODIFIER c.-1933C>T| S3
3 BAA02g42970 A02 35702030 C T upstream_gene_variant MODIFIER c.-671C>T| S51
4 BAA02g42970 A02 35702500 C T upstream_gene_variant MODIFIER c.-201C>T| S210
S225
5 BAA02g42970 A02 35703082 G A intron_variant MODIFIER c.81-291G>A| S19
6 BAA02g42970 A02 35703256 G A intron_variant MODIFIER c.81-117G>A| S294
7 BAA02g42970 A02 35703432 C T missense_variant MODERATE c.140C>T|p.Ala47Val S262
8 BAA02g42970 A02 35703452 G A missense_variant MODERATE c.160G>A|p.Glu54Lys S224
9 BAA02g42970 A02 35703492 G A missense_variant MODERATE c.200G>A|p.Arg67Lys S294
10 BAA02g42970 A02 35703941 C T synonymous_variant LOW c.399C>T|p.Tyr133Tyr S295
11 BAA02g42970 A02 35703981 G A missense_variant MODERATE c.439G>A|p.Val147Ile S223
12 BAA02g42970 A02 35704025 G A synonymous_variant LOW c.483G>A|p.Leu161Leu S294
13 BAA02g42970 A02 35704165 C T missense_variant&splice_region_variant MODERATE c.535C>T|p.Leu179Phe S289
S290
14 BAA02g42970 A02 35705293 G A intron_variant MODIFIER c.1203+80G>A| S19
15 BAA02g42970 A02 35706691 C T missense_variant MODERATE c.1883C>T|p.Ala628Val S226
16 BAA02g42970 A02 35707449 C T missense_variant MODERATE c.2273C>T|p.Ser758Phe S216
17 BAA02g42970 A02 35708677 G A synonymous_variant LOW c.2889G>A|p.Thr963Thr S56
18 BAA02g42970 A02 35708710 C T synonymous_variant LOW c.2922C>T|p.Ile974Ile S193
19 BAA02g42970 A02 35709295 C T stop_gained HIGH c.3325C>T|p.Gln1109* S179
20 BAA02g42970 A02 35709307 C T stop_gained HIGH c.3337C>T|p.Gln1113* S61
21 BAA02g42970 A02 35709352 C T downstream_gene_variant MODIFIER c.*31C>T| S144
22 BAA02g42970 A02 35710218 C T downstream_gene_variant MODIFIER c.*897C>T| S13
23 BAA02g42970 A02 35710813 G A downstream_gene_variant MODIFIER c.*1492G>A| S81
S85
24 BAA02g42970 A02 35710957 G A downstream_gene_variant MODIFIER c.*1636G>A| S180
25 BAA02g42970 A02 35711095 C T downstream_gene_variant MODIFIER c.*1774C>T| S301
S304