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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g16170 A05 8900415 C T upstream_gene_variant MODIFIER c.-4782C>T| S153
S213
2 BAA05g16170 A05 8906011 G A synonymous_variant LOW c.405G>A|p.Glu135Glu S275
3 BAA05g16170 A05 8906928 G A intron_variant MODIFIER c.735+186G>A| S245
4 BAA05g16170 A05 8907767 C T intron_variant MODIFIER c.735+1025C>T| S37
5 BAA05g16170 A05 8907801 C T intron_variant MODIFIER c.735+1059C>T| S71
6 BAA05g16170 A05 8908307 C T intron_variant MODIFIER c.735+1565C>T| S232
7 BAA05g16170 A05 8909877 G A intron_variant MODIFIER c.736-672G>A| S224
8 BAA05g16170 A05 8909882 G A intron_variant MODIFIER c.736-667G>A| S97
9 BAA05g16170 A05 8910392 G A intron_variant MODIFIER c.736-157G>A| S150
10 BAA05g16170 A05 8910590 G A synonymous_variant LOW c.777G>A|p.Gln259Gln S252
11 BAA05g16170 A05 8910675 C T intron_variant MODIFIER c.803-12C>T| S36
12 BAA05g16170 A05 8910998 G A missense_variant MODERATE c.1114G>A|p.Glu372Lys S280
13 BAA05g16170 A05 8911376 G A missense_variant MODERATE c.1492G>A|p.Glu498Lys S230
14 BAA05g16170 A05 8911578 C T missense_variant MODERATE c.1694C>T|p.Ser565Leu S177
15 BAA05g16170 A05 8912092 C T missense_variant MODERATE c.2134C>T|p.Arg712Cys S98
16 BAA05g16170 A05 8913214 G A downstream_gene_variant MODIFIER c.*506G>A| S132
S89