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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g35750 A06 23815589 G A downstream_gene_variant MODIFIER c.*3761C>T| S208
S93
2 BAA06g35750 A06 23816829 G A downstream_gene_variant MODIFIER c.*2521C>T| S209
3 BAA06g35750 A06 23817071 G A downstream_gene_variant MODIFIER c.*2279C>T| S146
4 BAA06g35750 A06 23817616 G A downstream_gene_variant MODIFIER c.*1734C>T| S126
5 BAA06g35750 A06 23817774 C T downstream_gene_variant MODIFIER c.*1576G>A| S266
6 BAA06g35750 A06 23818857 G A downstream_gene_variant MODIFIER c.*493C>T| S183
7 BAA06g35750 A06 23819719 C T intron_variant MODIFIER c.856-316G>A| S43
8 BAA06g35750 A06 23820114 C T intron_variant MODIFIER c.855+544G>A| S205
9 BAA06g35750 A06 23820965 G A intron_variant MODIFIER c.715-136C>T| S219
S72
10 BAA06g35750 A06 23821107 C T intron_variant MODIFIER c.715-278G>A| S252
11 BAA06g35750 A06 23821480 G A synonymous_variant LOW c.660C>T|p.Leu220Leu S149
12 BAA06g35750 A06 23821530 G A missense_variant MODERATE c.610C>T|p.Arg204Cys S192
13 BAA06g35750 A06 23821643 G A missense_variant MODERATE c.497C>T|p.Ala166Val S256
14 BAA06g35750 A06 23822253 G A intron_variant MODIFIER c.404-517C>T| S76
15 BAA06g35750 A06 23822442 C T intron_variant MODIFIER c.404-706G>A| S281
16 BAA06g35750 A06 23822578 C T intron_variant MODIFIER c.404-842G>A| S279
17 BAA06g35750 A06 23822589 C T intron_variant MODIFIER c.404-853G>A| S262
18 BAA06g35750 A06 23822908 G A intron_variant MODIFIER c.403+1018C>T| S69
19 BAA06g35750 A06 23823096 C T intron_variant MODIFIER c.403+830G>A| S105
S106
20 BAA06g35750 A06 23825393 G A upstream_gene_variant MODIFIER c.-78C>T| S191
21 BAA06g35750 A06 23825709 C T upstream_gene_variant MODIFIER c.-394G>A| S153
22 BAA06g35750 A06 23826250 C T upstream_gene_variant MODIFIER c.-935G>A| S43
23 BAA06g35750 A06 23826901 G A upstream_gene_variant MODIFIER c.-1586C>T| S73
24 BAA06g35750 A06 23828063 C T upstream_gene_variant MODIFIER c.-2748G>A| S112