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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g22880 A01 11611431 C T upstream_gene_variant MODIFIER c.-2392C>T| S18
2 BAA01g22880 A01 11612689 C T upstream_gene_variant MODIFIER c.-1134C>T| S19
3 BAA01g22880 A01 11612764 G A upstream_gene_variant MODIFIER c.-1059G>A| S246
4 BAA01g22880 A01 11613347 G A upstream_gene_variant MODIFIER c.-476G>A| S226
5 BAA01g22880 A01 11613424 C T upstream_gene_variant MODIFIER c.-399C>T| S135
6 BAA01g22880 A01 11613760 C T upstream_gene_variant MODIFIER c.-63C>T| S201
7 BAA01g22880 A01 11613789 C T upstream_gene_variant MODIFIER c.-34C>T| S148
S30
S31
8 BAA01g22880 A01 11613830 C T missense_variant MODERATE c.8C>T|p.Ser3Phe S282
9 BAA01g22880 A01 11614031 G A missense_variant MODERATE c.209G>A|p.Arg70Lys S119
10 BAA01g22880 A01 11618111 C T missense_variant MODERATE c.1148C>T|p.Thr383Ile S10
11 BAA01g22880 A01 11618378 G A missense_variant MODERATE c.1415G>A|p.Arg472His S121
12 BAA01g22880 A01 11618459 C T intron_variant MODIFIER c.1452+44C>T| S99
13 BAA01g22880 A01 11618658 C T synonymous_variant LOW c.1485C>T|p.Val495Val S104
S52
14 BAA01g22880 A01 11618788 G A missense_variant MODERATE c.1615G>A|p.Asp539Asn S292
15 BAA01g22880 A01 11619274 G A intron_variant MODIFIER c.1854-18G>A| S59
16 BAA01g22880 A01 11619920 C T missense_variant MODERATE c.2482C>T|p.Leu828Phe S179
17 BAA01g22880 A01 11622063 G A missense_variant MODERATE c.3032G>A|p.Arg1011His S274
18 BAA01g22880 A01 11622393 C T missense_variant MODERATE c.3362C>T|p.Ala1121Val S272
19 BAA01g22880 A01 11622897 G A synonymous_variant LOW c.3783G>A|p.Leu1261Leu S280
20 BAA01g22880 A01 11623010 C T missense_variant MODERATE c.3896C>T|p.Ser1299Phe S289
S290
21 BAA01g22880 A01 11623179 G A missense_variant MODERATE c.3958G>A|p.Asp1320Asn S131
22 BAA01g22880 A01 11623852 C T downstream_gene_variant MODIFIER c.*290C>T| S171
23 BAA01g22880 A01 11625262 G A downstream_gene_variant MODIFIER c.*1700G>A| S56