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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g07960 A04 5397496 C T upstream_gene_variant MODIFIER c.-4549C>T| S202
2 BAA04g07960 A04 5398299 C T upstream_gene_variant MODIFIER c.-3746C>T| S1
S90
3 BAA04g07960 A04 5398582 G A upstream_gene_variant MODIFIER c.-3463G>A| S77
S82
4 BAA04g07960 A04 5398634 G A upstream_gene_variant MODIFIER c.-3411G>A| S5
5 BAA04g07960 A04 5398982 C T upstream_gene_variant MODIFIER c.-3063C>T| S302
6 BAA04g07960 A04 5399747 C T upstream_gene_variant MODIFIER c.-2298C>T| S148
7 BAA04g07960 A04 5400007 C T upstream_gene_variant MODIFIER c.-2038C>T| S68
8 BAA04g07960 A04 5400794 C T upstream_gene_variant MODIFIER c.-1251C>T| S209
9 BAA04g07960 A04 5400944 G A upstream_gene_variant MODIFIER c.-1101G>A| S143
10 BAA04g07960 A04 5401710 C T upstream_gene_variant MODIFIER c.-335C>T| S9
11 BAA04g07960 A04 5402102 G A missense_variant MODERATE c.58G>A|p.Glu20Lys S133
12 BAA04g07960 A04 5403162 C T synonymous_variant LOW c.468C>T|p.Asn156Asn S82
S92
13 BAA04g07960 A04 5403205 G A missense_variant MODERATE c.511G>A|p.Glu171Lys S303
14 BAA04g07960 A04 5403482 A G intron_variant MODIFIER c.599-184A>G| S86
15 BAA04g07960 A04 5403518 G A intron_variant MODIFIER c.599-148G>A| S56
16 BAA04g07960 A04 5403542 G A intron_variant MODIFIER c.599-124G>A| S286
17 BAA04g07960 A04 5403751 C T synonymous_variant LOW c.684C>T|p.Val228Val S95
18 BAA04g07960 A04 5403989 G A missense_variant MODERATE c.847G>A|p.Ala283Thr S161
19 BAA04g07960 A04 5404108 C T intron_variant MODIFIER c.868-12C>T| S134
20 BAA04g07960 A04 5404238 G A missense_variant MODERATE c.986G>A|p.Arg329Lys S175
21 BAA04g07960 A04 5405280 G A synonymous_variant LOW c.1515G>A|p.Gln505Gln S38
22 BAA04g07960 A04 5406341 G A downstream_gene_variant MODIFIER c.*700G>A| S99
23 BAA04g07960 A04 5406892 C T downstream_gene_variant MODIFIER c.*1251C>T| S167
24 BAA04g07960 A04 5407074 C T downstream_gene_variant MODIFIER c.*1433C>T| S130
25 BAA04g07960 A04 5407475 C T downstream_gene_variant MODIFIER c.*1834C>T| S134