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 BAA02g06500 A02 2752366 G A downstream_gene_variant MODIFIER c.*1746C>T| S286
2 BAA02g06500 A02 2752595 C T downstream_gene_variant MODIFIER c.*1517G>A| S100
3 BAA02g06500 A02 2754696 G A synonymous_variant LOW c.5136C>T|p.Val1712Val S139
4 BAA02g06500 A02 2754948 G A missense_variant MODERATE c.5006C>T|p.Ala1669Val S246
5 BAA02g06500 A02 2755114 C T missense_variant MODERATE c.4840G>A|p.Asp1614Asn S274
6 BAA02g06500 A02 2755410 C T missense_variant MODERATE c.4621G>A|p.Asp1541Asn S108
7 BAA02g06500 A02 2756129 C T missense_variant MODERATE c.4069G>A|p.Asp1357Asn S240
8 BAA02g06500 A02 2756552 C T missense_variant MODERATE c.3818G>A|p.Arg1273Lys S46
9 BAA02g06500 A02 2758041 G A stop_gained HIGH c.3073C>T|p.Gln1025* S202
10 BAA02g06500 A02 2758286 G A missense_variant MODERATE c.2939C>T|p.Pro980Leu S157
11 BAA02g06500 A02 2759798 C T synonymous_variant LOW c.1848G>A|p.Glu616Glu S38
12 BAA02g06500 A02 2760221 C T intron_variant MODIFIER c.1485+51G>A| S216
13 BAA02g06500 A02 2761317 G A intron_variant MODIFIER c.981+125C>T| S153
S257
S263
14 BAA02g06500 A02 2761978 C T missense_variant MODERATE c.601G>A|p.Asp201Asn S109
15 BAA02g06500 A02 2762603 C T splice_acceptor_variant&intron_variant HIGH c.270-1G>A| S123
16 BAA02g06500 A02 2762906 C T intron_variant MODIFIER c.269+210G>A| S224
17 BAA02g06500 A02 2763081 G A intron_variant MODIFIER c.269+35C>T| S238
18 BAA02g06500 A02 2763105 G A intron_variant MODIFIER c.269+11C>T| S190
19 BAA02g06500 A02 2764245 G A upstream_gene_variant MODIFIER c.-861C>T| S244
20 BAA02g06500 A02 2765452 G A upstream_gene_variant MODIFIER c.-2068C>T| S23
21 BAA02g06500 A02 2765678 G A upstream_gene_variant MODIFIER c.-2294C>T| S170