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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g21360 A01 10595858 C T synonymous_variant LOW c.504C>T|p.Tyr168Tyr S53
2 BAA01g21360 A01 10595961 C T missense_variant MODERATE c.538C>T|p.Pro180Ser S289
S290
3 BAA01g21360 A01 10596190 C T missense_variant MODERATE c.679C>T|p.Pro227Ser S46
4 BAA01g21360 A01 10597343 G A missense_variant MODERATE c.1274G>A|p.Gly425Glu S181
5 BAA01g21360 A01 10598679 G A missense_variant MODERATE c.1945G>A|p.Glu649Lys S240
6 BAA01g21360 A01 10598712 G A missense_variant MODERATE c.1978G>A|p.Gly660Arg S262
7 BAA01g21360 A01 10598832 G A missense_variant MODERATE c.2029G>A|p.Gly677Arg S71
8 BAA01g21360 A01 10598987 G A synonymous_variant LOW c.2184G>A|p.Glu728Glu S116
9 BAA01g21360 A01 10601381 C T synonymous_variant LOW c.2794C>T|p.Leu932Leu S205
10 BAA01g21360 A01 10601419 C T synonymous_variant LOW c.2832C>T|p.Ser944Ser S179
11 BAA01g21360 A01 10603095 C T downstream_gene_variant MODIFIER c.*1658C>T| S19
12 BAA01g21360 A01 10603516 G T downstream_gene_variant MODIFIER c.*2079G>T| S98
13 BAA01g21360 A01 10603537 C T downstream_gene_variant MODIFIER c.*2100C>T| S179