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 BAA02g40990 A02 34387946 G A upstream_gene_variant MODIFIER c.-4917G>A| S246
2 BAA02g40990 A02 34388000 G A upstream_gene_variant MODIFIER c.-4863G>A| S268
3 BAA02g40990 A02 34388147 G A upstream_gene_variant MODIFIER c.-4716G>A| S71
4 BAA02g40990 A02 34388468 C T upstream_gene_variant MODIFIER c.-4395C>T| S121
5 BAA02g40990 A02 34389416 T G upstream_gene_variant MODIFIER c.-3447T>G| S27
6 BAA02g40990 A02 34389701 A T upstream_gene_variant MODIFIER c.-3162A>T| S13
7 BAA02g40990 A02 34391401 C T upstream_gene_variant MODIFIER c.-1462C>T| S120
8 BAA02g40990 A02 34391774 C T upstream_gene_variant MODIFIER c.-1089C>T| S112
9 BAA02g40990 A02 34392051 C T upstream_gene_variant MODIFIER c.-812C>T| S112
10 BAA02g40990 A02 34392223 C T upstream_gene_variant MODIFIER c.-640C>T| S266
11 BAA02g40990 A02 34392564 C G upstream_gene_variant MODIFIER c.-299C>G| S217
S248
12 BAA02g40990 A02 34392906 C T missense_variant MODERATE c.44C>T|p.Ser15Leu S279
13 BAA02g40990 A02 34392921 C T missense_variant MODERATE c.59C>T|p.Ser20Leu S185
14 BAA02g40990 A02 34392978 C T missense_variant MODERATE c.116C>T|p.Thr39Ile S100
15 BAA02g40990 A02 34393072 G A stop_gained HIGH c.210G>A|p.Trp70* S113
16 BAA02g40990 A02 34394019 C T missense_variant MODERATE c.1157C>T|p.Thr386Ile S270
17 BAA02g40990 A02 34394036 G A missense_variant MODERATE c.1174G>A|p.Asp392Asn S37
18 BAA02g40990 A02 34394743 C T missense_variant MODERATE c.1531C>T|p.Leu511Phe S270
19 BAA02g40990 A02 34396365 C T missense_variant MODERATE c.1891C>T|p.Arg631Cys S133
20 BAA02g40990 A02 34396446 G A downstream_gene_variant MODIFIER c.*28G>A| S192
S232
21 BAA02g40990 A02 34396926 G A downstream_gene_variant MODIFIER c.*508G>A| S245
22 BAA02g40990 A02 34398591 C T downstream_gene_variant MODIFIER c.*2173C>T| S295
23 BAA02g40990 A02 34399056 C T downstream_gene_variant MODIFIER c.*2638C>T| S34
24 BAA02g40990 A02 34400291 G A downstream_gene_variant MODIFIER c.*3873G>A| S71
25 BAA02g40990 A02 34400435 C T downstream_gene_variant MODIFIER c.*4017C>T| S189