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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g35290 A01 23624211 C T missense_variant MODERATE c.68C>T|p.Ser23Phe S139
2 BAA01g35290 A01 23624400 C T missense_variant MODERATE c.257C>T|p.Ser86Phe S234
3 BAA01g35290 A01 23625017 G A missense_variant MODERATE c.706G>A|p.Gly236Ser S135
4 BAA01g35290 A01 23626392 G A missense_variant MODERATE c.1337G>A|p.Arg446Lys S158
5 BAA01g35290 A01 23626745 C T missense_variant MODERATE c.1468C>T|p.Pro490Ser S286
6 BAA01g35290 A01 23626906 G A missense_variant MODERATE c.1550G>A|p.Gly517Glu S202
7 BAA01g35290 A01 23626971 G A missense_variant MODERATE c.1615G>A|p.Gly539Ser S244
8 BAA01g35290 A01 23628880 G A downstream_gene_variant MODIFIER c.*1871G>A| S99
9 BAA01g35290 A01 23628932 C T downstream_gene_variant MODIFIER c.*1923C>T| S153
10 BAA01g35290 A01 23629225 G A downstream_gene_variant MODIFIER c.*2216G>A| S299
11 BAA01g35290 A01 23629226 G A downstream_gene_variant MODIFIER c.*2217G>A| S60
12 BAA01g35290 A01 23629233 C T downstream_gene_variant MODIFIER c.*2224C>T| S204
13 BAA01g35290 A01 23631785 C T downstream_gene_variant MODIFIER c.*4776C>T| S213