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 BAA03g09220 A03 3821230 C T downstream_gene_variant MODIFIER c.*4708G>A| S18
2 BAA03g09220 A03 3821492 C T downstream_gene_variant MODIFIER c.*4446G>A| S279
3 BAA03g09220 A03 3825017 G A downstream_gene_variant MODIFIER c.*921C>T| S192
4 BAA03g09220 A03 3825514 G A downstream_gene_variant MODIFIER c.*424C>T| S183
S198
5 BAA03g09220 A03 3826297 C T missense_variant MODERATE c.3739G>A|p.Asp1247Asn S260
6 BAA03g09220 A03 3826591 C T missense_variant MODERATE c.3445G>A|p.Glu1149Lys S121
7 BAA03g09220 A03 3826812 G A missense_variant MODERATE c.3224C>T|p.Ser1075Phe S41
8 BAA03g09220 A03 3827514 G A missense_variant MODERATE c.2875C>T|p.Leu959Phe S54
9 BAA03g09220 A03 3827610 G A synonymous_variant LOW c.2779C>T|p.Leu927Leu S148
10 BAA03g09220 A03 3827637 C T missense_variant MODERATE c.2752G>A|p.Asp918Asn S65
11 BAA03g09220 A03 3828037 C T synonymous_variant LOW c.2352G>A|p.Gln784Gln S203
12 BAA03g09220 A03 3828576 G A synonymous_variant LOW c.1944C>T|p.Thr648Thr S109
13 BAA03g09220 A03 3828792 C T synonymous_variant LOW c.1728G>A|p.Gln576Gln S35
14 BAA03g09220 A03 3828949 G A missense_variant MODERATE c.1571C>T|p.Pro524Leu S36
15 BAA03g09220 A03 3829095 C T synonymous_variant LOW c.1425G>A|p.Ala475Ala S144
16 BAA03g09220 A03 3829586 G A stop_gained HIGH c.934C>T|p.Gln312* S105
S106
17 BAA03g09220 A03 3830047 C T missense_variant MODERATE c.473G>A|p.Arg158His S4
S6
18 BAA03g09220 A03 3831111 C T missense_variant MODERATE c.101G>A|p.Ser34Asn S174
S265
S27
19 BAA03g09220 A03 3831704 C T upstream_gene_variant MODIFIER c.-399G>A| S276
20 BAA03g09220 A03 3834548 C T upstream_gene_variant MODIFIER c.-3243G>A| S58
21 BAA03g09220 A03 3834600 C T upstream_gene_variant MODIFIER c.-3295G>A| S32