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 BAA06g27540 A06 18906864 C T upstream_gene_variant MODIFIER c.-4037C>T| S296
2 BAA06g27540 A06 18906878 G A upstream_gene_variant MODIFIER c.-4023G>A| S308
3 BAA06g27540 A06 18908472 C T upstream_gene_variant MODIFIER c.-2429C>T| S164
4 BAA06g27540 A06 18908581 G A upstream_gene_variant MODIFIER c.-2320G>A| S204
5 BAA06g27540 A06 18909595 G A upstream_gene_variant MODIFIER c.-1306G>A| S257
6 BAA06g27540 A06 18910949 C T missense_variant MODERATE c.49C>T|p.Pro17Ser S286
7 BAA06g27540 A06 18911082 C T missense_variant MODERATE c.68C>T|p.Pro23Leu S252
8 BAA06g27540 A06 18911094 C T missense_variant MODERATE c.80C>T|p.Pro27Leu S77
9 BAA06g27540 A06 18911320 C T synonymous_variant LOW c.306C>T|p.Phe102Phe S45
10 BAA06g27540 A06 18912205 G A missense_variant MODERATE c.712G>A|p.Glu238Lys S268
11 BAA06g27540 A06 18912224 G A missense_variant MODERATE c.731G>A|p.Ser244Asn S240
12 BAA06g27540 A06 18912637 G A missense_variant MODERATE c.868G>A|p.Glu290Lys S264
13 BAA06g27540 A06 18913732 G A splice_acceptor_variant&intron_variant HIGH c.1075-1G>A| S50