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


Gene ID

Results: 1 - 28 of 28 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g20400 A01 10042732 C T downstream_gene_variant MODIFIER c.*1986G>A| S42
2 BAA01g20400 A01 10043788 C T downstream_gene_variant MODIFIER c.*930G>A| S128
3 BAA01g20400 A01 10043926 C T downstream_gene_variant MODIFIER c.*792G>A| S176
4 BAA01g20400 A01 10044185 G A downstream_gene_variant MODIFIER c.*533C>T| S245
5 BAA01g20400 A01 10044444 C T downstream_gene_variant MODIFIER c.*274G>A| S247
6 BAA01g20400 A01 10045572 C T intron_variant MODIFIER c.2614-771G>A| S279
7 BAA01g20400 A01 10045586 G A intron_variant MODIFIER c.2614-785C>T| S74
8 BAA01g20400 A01 10046310 G A intron_variant MODIFIER c.2613+449C>T| S103
9 BAA01g20400 A01 10046524 C T intron_variant MODIFIER c.2613+235G>A| S245
10 BAA01g20400 A01 10046572 C T intron_variant MODIFIER c.2613+187G>A| S70
11 BAA01g20400 A01 10047115 G A synonymous_variant LOW c.2257C>T|p.Leu753Leu S209
12 BAA01g20400 A01 10047623 C T synonymous_variant LOW c.1749G>A|p.Lys583Lys S213
13 BAA01g20400 A01 10047816 C T missense_variant MODERATE c.1651G>A|p.Ala551Thr S27
14 BAA01g20400 A01 10047867 T C missense_variant MODERATE c.1600A>G|p.Ile534Val S198
15 BAA01g20400 A01 10048216 C T synonymous_variant LOW c.1251G>A|p.Ser417Ser S198
16 BAA01g20400 A01 10048333 G A synonymous_variant LOW c.1134C>T|p.Asp378Asp S281
17 BAA01g20400 A01 10049077 C T stop_gained HIGH c.390G>A|p.Trp130* S228
18 BAA01g20400 A01 10049143 C T stop_gained HIGH c.324G>A|p.Trp108* S148
S30
S31
19 BAA01g20400 A01 10049375 C T missense_variant MODERATE c.92G>A|p.Ser31Asn S228
20 BAA01g20400 A01 10049414 G T missense_variant MODERATE c.53C>A|p.Thr18Asn S116
21 BAA01g20400 A01 10049517 G A upstream_gene_variant MODIFIER c.-51C>T| S274
22 BAA01g20400 A01 10049647 G A upstream_gene_variant MODIFIER c.-181C>T| S202
23 BAA01g20400 A01 10049719 G A upstream_gene_variant MODIFIER c.-253C>T| S14
24 BAA01g20400 A01 10049883 G A upstream_gene_variant MODIFIER c.-417C>T| S245
25 BAA01g20400 A01 10049978 C T upstream_gene_variant MODIFIER c.-512G>A| S54