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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g19690 A06 10217206 G A upstream_gene_variant MODIFIER c.-4457G>A| S153
2 BAA06g19690 A06 10217421 C T upstream_gene_variant MODIFIER c.-4242C>T| S293
3 BAA06g19690 A06 10217511 C T upstream_gene_variant MODIFIER c.-4152C>T| S74
4 BAA06g19690 A06 10218307 G A upstream_gene_variant MODIFIER c.-3356G>A| S269
5 BAA06g19690 A06 10218488 C T upstream_gene_variant MODIFIER c.-3175C>T| S155
S211
6 BAA06g19690 A06 10218716 G A upstream_gene_variant MODIFIER c.-2947G>A| S81
S85
7 BAA06g19690 A06 10218823 T A upstream_gene_variant MODIFIER c.-2840T>A| S292
8 BAA06g19690 A06 10219653 G A upstream_gene_variant MODIFIER c.-2010G>A| S243
S299
9 BAA06g19690 A06 10221475 C T upstream_gene_variant MODIFIER c.-188C>T| S37
10 BAA06g19690 A06 10221660 G A upstream_gene_variant MODIFIER c.-3G>A| S133
11 BAA06g19690 A06 10221895 C T missense_variant MODERATE c.158C>T|p.Ser53Phe S291
12 BAA06g19690 A06 10221906 G A missense_variant MODERATE c.169G>A|p.Glu57Lys S108
13 BAA06g19690 A06 10223110 C T splice_region_variant&intron_variant LOW c.654-7C>T| S242
14 BAA06g19690 A06 10223320 C T missense_variant MODERATE c.752C>T|p.Ser251Phe S189
15 BAA06g19690 A06 10223336 G A synonymous_variant LOW c.768G>A|p.Leu256Leu S13
16 BAA06g19690 A06 10223839 G A missense_variant MODERATE c.847G>A|p.Glu283Lys S284
17 BAA06g19690 A06 10226572 G A downstream_gene_variant MODIFIER c.*2695G>A| S275