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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g04800 A02 2083866 G A missense_variant MODERATE c.782G>A|p.Ser261Asn S246
2 BAA02g04800 A02 2084093 C T missense_variant MODERATE c.1009C>T|p.Pro337Ser S250
3 BAA02g04800 A02 2084130 C T missense_variant MODERATE c.1046C>T|p.Pro349Leu S179
4 BAA02g04800 A02 2084178 C T missense_variant MODERATE c.1094C>T|p.Thr365Ile S216
5 BAA02g04800 A02 2084240 C T missense_variant MODERATE c.1156C>T|p.Pro386Ser S233
6 BAA02g04800 A02 2084524 G A missense_variant MODERATE c.1367G>A|p.Arg456Gln S107
7 BAA02g04800 A02 2085688 G A missense_variant MODERATE c.1964G>A|p.Ser655Asn S266
8 BAA02g04800 A02 2086399 C T missense_variant MODERATE c.2675C>T|p.Ala892Val S157
9 BAA02g04800 A02 2087034 C T missense_variant MODERATE c.3026C>T|p.Thr1009Met S46
10 BAA02g04800 A02 2088027 C T missense_variant MODERATE c.3616C>T|p.Leu1206Phe S138
11 BAA02g04800 A02 2088744 C T missense_variant MODERATE c.4019C>T|p.Ala1340Val S278
12 BAA02g04800 A02 2089437 C T missense_variant MODERATE c.4598C>T|p.Ser1533Phe S240
13 BAA02g04800 A02 2089917 C T downstream_gene_variant MODIFIER c.*464C>T| S153
14 BAA02g04800 A02 2090423 C T downstream_gene_variant MODIFIER c.*970C>T| S18