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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g01070 A08 768540 G A missense_variant MODERATE c.5147C>T|p.Ser1716Phe S56
2 BAA08g01070 A08 768557 C T synonymous_variant LOW c.5130G>A|p.Gln1710Gln S74
3 BAA08g01070 A08 768714 G A missense_variant MODERATE c.5054C>T|p.Ser1685Phe S38
4 BAA08g01070 A08 769857 G A missense_variant MODERATE c.4567C>T|p.Pro1523Ser S39
5 BAA08g01070 A08 771186 G A missense_variant MODERATE c.3869C>T|p.Thr1290Ile S202
6 BAA08g01070 A08 771635 G A intron_variant MODIFIER c.3741+164C>T| S61
7 BAA08g01070 A08 773338 C T splice_region_variant&synonymous_variant LOW c.3006G>A|p.Lys1002Lys S136
8 BAA08g01070 A08 774394 C T missense_variant MODERATE c.2338G>A|p.Val780Ile S180
9 BAA08g01070 A08 774526 C T missense_variant MODERATE c.2276G>A|p.Gly759Glu S177
10 BAA08g01070 A08 774641 C T intron_variant MODIFIER c.2170-9G>A| S48
11 BAA08g01070 A08 774836 G A intron_variant MODIFIER c.2170-204C>T| S186
12 BAA08g01070 A08 776285 C T intron_variant MODIFIER c.1530-68G>A| S171
13 BAA08g01070 A08 776669 C T intron_variant MODIFIER c.1529+38G>A| S267
14 BAA08g01070 A08 778333 G A synonymous_variant LOW c.993C>T|p.Cys331Cys S58
15 BAA08g01070 A08 781032 G A upstream_gene_variant MODIFIER c.-289C>T| S69
16 BAA08g01070 A08 781151 G A upstream_gene_variant MODIFIER c.-408C>T| S62
S70
17 BAA08g01070 A08 781246 G A upstream_gene_variant MODIFIER c.-503C>T| S238
18 BAA08g01070 A08 781732 G T upstream_gene_variant MODIFIER c.-989C>A| S56
19 BAA08g01070 A08 782043 C T upstream_gene_variant MODIFIER c.-1300G>A| S243
S299
20 BAA08g01070 A08 783277 G A upstream_gene_variant MODIFIER c.-2534C>T| S256
21 BAA08g01070 A08 785333 C T upstream_gene_variant MODIFIER c.-4590G>A| S52