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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g21690 A06 11686025 G A downstream_gene_variant MODIFIER c.*3588C>T| S50
2 BAA06g21690 A06 11686041 C T downstream_gene_variant MODIFIER c.*3572G>A| S112
3 BAA06g21690 A06 11687984 G A downstream_gene_variant MODIFIER c.*1629C>T| S213
4 BAA06g21690 A06 11688877 G A downstream_gene_variant MODIFIER c.*736C>T| S81
S85
5 BAA06g21690 A06 11689030 G A downstream_gene_variant MODIFIER c.*583C>T| S143
6 BAA06g21690 A06 11689033 G A downstream_gene_variant MODIFIER c.*580C>T| S271
7 BAA06g21690 A06 11689121 C T downstream_gene_variant MODIFIER c.*492G>A| S58
8 BAA06g21690 A06 11689214 C T downstream_gene_variant MODIFIER c.*399G>A| S168
S170
S296
9 BAA06g21690 A06 11689230 C T downstream_gene_variant MODIFIER c.*383G>A| S120
10 BAA06g21690 A06 11689551 C T downstream_gene_variant MODIFIER c.*62G>A| S286
S291
11 BAA06g21690 A06 11689553 C T downstream_gene_variant MODIFIER c.*60G>A| S298
12 BAA06g21690 A06 11689727 C T synonymous_variant LOW c.2061G>A|p.Glu687Glu S155
13 BAA06g21690 A06 11690340 C T missense_variant MODERATE c.1837G>A|p.Gly613Arg S189
14 BAA06g21690 A06 11690866 C T missense_variant MODERATE c.1546G>A|p.Ala516Thr S15
S3
15 BAA06g21690 A06 11691140 G A intron_variant MODIFIER c.1392-33C>T| S219
16 BAA06g21690 A06 11691229 G A missense_variant MODERATE c.1354C>T|p.Pro452Ser S273
17 BAA06g21690 A06 11691859 G A synonymous_variant LOW c.996C>T|p.Asn332Asn S240
18 BAA06g21690 A06 11691957 C T missense_variant MODERATE c.898G>A|p.Gly300Ser S16
19 BAA06g21690 A06 11696268 A T upstream_gene_variant MODIFIER c.-2812T>A| S33
20 BAA06g21690 A06 11696383 C T upstream_gene_variant MODIFIER c.-2927G>A| S189