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


Gene ID

Results: 1 - 50 of 50 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAS13g00230 Scaffold13 5054891 G A upstream_gene_variant MODIFIER c.-4676G>A| S56
2 BAS13g00230 Scaffold13 5055145 G A upstream_gene_variant MODIFIER c.-4422G>A| S291
3 BAS13g00230 Scaffold13 5055162 G A upstream_gene_variant MODIFIER c.-4405G>A| S100
4 BAS13g00230 Scaffold13 5055326 C T upstream_gene_variant MODIFIER c.-4241C>T| S65
5 BAS13g00230 Scaffold13 5055636 G A upstream_gene_variant MODIFIER c.-3931G>A| S17
6 BAS13g00230 Scaffold13 5055734 G A upstream_gene_variant MODIFIER c.-3833G>A| S167
7 BAS13g00230 Scaffold13 5055755 G A upstream_gene_variant MODIFIER c.-3812G>A| S84
8 BAS13g00230 Scaffold13 5057372 G A upstream_gene_variant MODIFIER c.-2195G>A| S257
9 BAS13g00230 Scaffold13 5057502 G A upstream_gene_variant MODIFIER c.-2065G>A| S249
10 BAS13g00230 Scaffold13 5057735 C T upstream_gene_variant MODIFIER c.-1832C>T| S155
S211
11 BAS13g00230 Scaffold13 5057814 C T upstream_gene_variant MODIFIER c.-1753C>T| S255
12 BAS13g00230 Scaffold13 5057817 T A upstream_gene_variant MODIFIER c.-1750T>A| S213
13 BAS13g00230 Scaffold13 5057952 C T upstream_gene_variant MODIFIER c.-1615C>T| S183
S198
14 BAS13g00230 Scaffold13 5058167 C T upstream_gene_variant MODIFIER c.-1400C>T| S59
15 BAS13g00230 Scaffold13 5058327 C T upstream_gene_variant MODIFIER c.-1240C>T| S161
16 BAS13g00230 Scaffold13 5058389 A T upstream_gene_variant MODIFIER c.-1178A>T| S61
17 BAS13g00230 Scaffold13 5058414 C T upstream_gene_variant MODIFIER c.-1153C>T| S65
18 BAS13g00230 Scaffold13 5058459 C T upstream_gene_variant MODIFIER c.-1108C>T| S133
19 BAS13g00230 Scaffold13 5058764 C T upstream_gene_variant MODIFIER c.-803C>T| S160
20 BAS13g00230 Scaffold13 5059325 C T upstream_gene_variant MODIFIER c.-242C>T| S267
21 BAS13g00230 Scaffold13 5060607 C T intron_variant MODIFIER c.686-9C>T| S146
22 BAS13g00230 Scaffold13 5061116 C T missense_variant MODERATE c.1106C>T|p.Ser369Phe S230
23 BAS13g00230 Scaffold13 5061519 G A missense_variant MODERATE c.1420G>A|p.Glu474Lys S130
24 BAS13g00230 Scaffold13 5061687 C T downstream_gene_variant MODIFIER c.*160C>T| S47
25 BAS13g00230 Scaffold13 5061712 G A downstream_gene_variant MODIFIER c.*185G>A| S175