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 BAA05g24650 A05 29660267 G A upstream_gene_variant MODIFIER c.-4908G>A| S160
2 BAA05g24650 A05 29660293 G A upstream_gene_variant MODIFIER c.-4882G>A| S296
3 BAA05g24650 A05 29660328 C T upstream_gene_variant MODIFIER c.-4847C>T| S98
4 BAA05g24650 A05 29660489 C T upstream_gene_variant MODIFIER c.-4686C>T| S181
5 BAA05g24650 A05 29660571 G A upstream_gene_variant MODIFIER c.-4604G>A| S266
6 BAA05g24650 A05 29661282 G A upstream_gene_variant MODIFIER c.-3893G>A| S48
7 BAA05g24650 A05 29661696 G A upstream_gene_variant MODIFIER c.-3479G>A| S125
8 BAA05g24650 A05 29661802 G A upstream_gene_variant MODIFIER c.-3373G>A| S54
9 BAA05g24650 A05 29664180 G T upstream_gene_variant MODIFIER c.-995G>T| S153
S213
10 BAA05g24650 A05 29664300 C T upstream_gene_variant MODIFIER c.-875C>T| S241
11 BAA05g24650 A05 29664750 G A upstream_gene_variant MODIFIER c.-425G>A| S293
12 BAA05g24650 A05 29664854 C T upstream_gene_variant MODIFIER c.-321C>T| S100
13 BAA05g24650 A05 29665622 C T missense_variant MODERATE c.370C>T|p.Arg124Cys S92
14 BAA05g24650 A05 29665840 C T synonymous_variant LOW c.588C>T|p.Asp196Asp S157
15 BAA05g24650 A05 29666446 C T synonymous_variant LOW c.1194C>T|p.Ser398Ser S294
16 BAA05g24650 A05 29667417 G A missense_variant MODERATE c.2165G>A|p.Arg722Lys S144
17 BAA05g24650 A05 29667881 C T synonymous_variant LOW c.2629C>T|p.Leu877Leu S175
18 BAA05g24650 A05 29669089 G A synonymous_variant LOW c.3837G>A|p.Glu1279Glu S246
19 BAA05g24650 A05 29669151 C T missense_variant MODERATE c.3899C>T|p.Thr1300Ile S169
S61
20 BAA05g24650 A05 29669339 C T splice_region_variant&intron_variant LOW c.4080+7C>T| S166
21 BAA05g24650 A05 29669487 C T missense_variant MODERATE c.4127C>T|p.Thr1376Ile S207