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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g28440 A10 21778686 G A upstream_gene_variant MODIFIER c.-2978G>A| S278
2 BAA10g28440 A10 21779406 G A upstream_gene_variant MODIFIER c.-2258G>A| S127
3 BAA10g28440 A10 21779688 C T upstream_gene_variant MODIFIER c.-1976C>T| S301
S304
4 BAA10g28440 A10 21780631 G A upstream_gene_variant MODIFIER c.-1033G>A| S181
5 BAA10g28440 A10 21780730 C T upstream_gene_variant MODIFIER c.-934C>T| S13
S168
S219
S279
S72
6 BAA10g28440 A10 21781346 G A upstream_gene_variant MODIFIER c.-318G>A| S199
7 BAA10g28440 A10 21781568 G A upstream_gene_variant MODIFIER c.-96G>A| S100
8 BAA10g28440 A10 21781807 C T synonymous_variant LOW c.144C>T|p.Val48Val S129
9 BAA10g28440 A10 21782987 G A intron_variant MODIFIER c.185+1139G>A| S57
10 BAA10g28440 A10 21784551 C T intron_variant MODIFIER c.243+177C>T| S295
11 BAA10g28440 A10 21785525 C T intron_variant MODIFIER c.489+100C>T| S295
12 BAA10g28440 A10 21785641 C T intron_variant MODIFIER c.489+216C>T| S68
13 BAA10g28440 A10 21787527 G A intron_variant MODIFIER c.570+1574G>A| S217
14 BAA10g28440 A10 21788865 G A intron_variant MODIFIER c.571-252G>A| S88
15 BAA10g28440 A10 21789116 G A splice_acceptor_variant&intron_variant HIGH c.571-1G>A| S134
16 BAA10g28440 A10 21789253 G A missense_variant MODERATE c.707G>A|p.Gly236Glu S136
17 BAA10g28440 A10 21789649 G A synonymous_variant LOW c.774G>A|p.Val258Val S127
18 BAA10g28440 A10 21789764 C T missense_variant MODERATE c.889C>T|p.Pro297Ser S18
19 BAA10g28440 A10 21790159 C T downstream_gene_variant MODIFIER c.*207C>T| S157
20 BAA10g28440 A10 21790450 G A downstream_gene_variant MODIFIER c.*498G>A| S233
21 BAA10g28440 A10 21791000 G A downstream_gene_variant MODIFIER c.*1048G>A| S132
S137
S215
S89
22 BAA10g28440 A10 21794201 C T downstream_gene_variant MODIFIER c.*4249C>T| S51