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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g46060 A09 50996470 C T upstream_gene_variant MODIFIER c.-4501C>T| S295
2 BAA09g46060 A09 50996884 C T upstream_gene_variant MODIFIER c.-4087C>T| S163
3 BAA09g46060 A09 50998294 G A upstream_gene_variant MODIFIER c.-2677G>A| S175
4 BAA09g46060 A09 50998806 G A upstream_gene_variant MODIFIER c.-2165G>A| S175
5 BAA09g46060 A09 50999605 C T upstream_gene_variant MODIFIER c.-1366C>T| S206
S26
6 BAA09g46060 A09 51000475 G A upstream_gene_variant MODIFIER c.-496G>A| S4
7 BAA09g46060 A09 51001022 G A missense_variant MODERATE c.52G>A|p.Gly18Ser S143
8 BAA09g46060 A09 51001248 C T missense_variant MODERATE c.278C>T|p.Ser93Phe S18
9 BAA09g46060 A09 51002078 C T missense_variant MODERATE c.1108C>T|p.Pro370Ser S122
10 BAA09g46060 A09 51002176 C T synonymous_variant LOW c.1206C>T|p.Ser402Ser S297
11 BAA09g46060 A09 51002387 C T missense_variant MODERATE c.1417C>T|p.Pro473Ser S40
S49
12 BAA09g46060 A09 51002411 C T missense_variant MODERATE c.1441C>T|p.Pro481Ser S219
13 BAA09g46060 A09 51004414 C T downstream_gene_variant MODIFIER c.*1272C>T| S205
14 BAA09g46060 A09 51006182 C T downstream_gene_variant MODIFIER c.*3040C>T| S152
15 BAA09g46060 A09 51006598 G A downstream_gene_variant MODIFIER c.*3456G>A| S127
16 BAA09g46060 A09 51006991 C T downstream_gene_variant MODIFIER c.*3849C>T| S205
17 BAA09g46060 A09 51007108 G A downstream_gene_variant MODIFIER c.*3966G>A| S57
18 BAA09g46060 A09 51007272 G A downstream_gene_variant MODIFIER c.*4130G>A| S59
19 BAA09g46060 A09 51007576 G A downstream_gene_variant MODIFIER c.*4434G>A| S265