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 BAA09g32470 A09 41142772 C T synonymous_variant LOW c.117C>T|p.Asn39Asn S95
2 BAA09g32470 A09 41143226 C T missense_variant MODERATE c.571C>T|p.Arg191Cys S30
S31
3 BAA09g32470 A09 41143443 C T missense_variant MODERATE c.788C>T|p.Pro263Leu S18
4 BAA09g32470 A09 41143545 C T missense_variant MODERATE c.890C>T|p.Ser297Phe S255
5 BAA09g32470 A09 41144226 G A downstream_gene_variant MODIFIER c.*584G>A| S51
6 BAA09g32470 A09 41144459 G A downstream_gene_variant MODIFIER c.*817G>A| S172
S217
7 BAA09g32470 A09 41145042 G A downstream_gene_variant MODIFIER c.*1400G>A| S45
8 BAA09g32470 A09 41145816 C T downstream_gene_variant MODIFIER c.*2174C>T| S169
9 BAA09g32470 A09 41146348 G A downstream_gene_variant MODIFIER c.*2706G>A| S13
10 BAA09g32470 A09 41146494 C T downstream_gene_variant MODIFIER c.*2852C>T| S242
11 BAA09g32470 A09 41146576 G A downstream_gene_variant MODIFIER c.*2934G>A| S57
12 BAA09g32470 A09 41146990 G A downstream_gene_variant MODIFIER c.*3348G>A| S297
13 BAA09g32470 A09 41148312 G A downstream_gene_variant MODIFIER c.*4670G>A| S289
S290