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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g08160 A10 5555879 G A upstream_gene_variant MODIFIER c.-4989G>A| S85
2 BAA10g08160 A10 5555898 G A upstream_gene_variant MODIFIER c.-4970G>A| S208
S219
3 BAA10g08160 A10 5556138 C T upstream_gene_variant MODIFIER c.-4730C>T| S155
S211
4 BAA10g08160 A10 5556144 G A upstream_gene_variant MODIFIER c.-4724G>A| S25
5 BAA10g08160 A10 5556298 G A upstream_gene_variant MODIFIER c.-4570G>A| S118
S67
6 BAA10g08160 A10 5556699 C T upstream_gene_variant MODIFIER c.-4169C>T| S308
7 BAA10g08160 A10 5556840 G A upstream_gene_variant MODIFIER c.-4028G>A| S273
8 BAA10g08160 A10 5556871 G A upstream_gene_variant MODIFIER c.-3997G>A| S245
9 BAA10g08160 A10 5560873 G A synonymous_variant LOW c.6G>A|p.Glu2Glu S125
10 BAA10g08160 A10 5564378 G A synonymous_variant LOW c.453G>A|p.Glu151Glu S152
11 BAA10g08160 A10 5565806 C T synonymous_variant LOW c.669C>T|p.Leu223Leu S142
12 BAA10g08160 A10 5565915 G A missense_variant MODERATE c.778G>A|p.Ala260Thr S262
13 BAA10g08160 A10 5565979 G A missense_variant MODERATE c.842G>A|p.Ser281Asn S76
14 BAA10g08160 A10 5566661 G A splice_acceptor_variant&intron_variant HIGH c.971-1G>A| S64
15 BAA10g08160 A10 5567000 G A missense_variant MODERATE c.1309G>A|p.Val437Met S120
S122
S266
S9
16 BAA10g08160 A10 5567204 G A downstream_gene_variant MODIFIER c.*91G>A| S128
17 BAA10g08160 A10 5567437 C T downstream_gene_variant MODIFIER c.*324C>T| S187
18 BAA10g08160 A10 5567630 C T downstream_gene_variant MODIFIER c.*517C>T| S237
19 BAA10g08160 A10 5567822 C T downstream_gene_variant MODIFIER c.*709C>T| S270
20 BAA10g08160 A10 5568832 C T downstream_gene_variant MODIFIER c.*1719C>T| S237
21 BAA10g08160 A10 5571006 G A downstream_gene_variant MODIFIER c.*3893G>A| S36
22 BAA10g08160 A10 5571044 G A downstream_gene_variant MODIFIER c.*3931G>A| S262
23 BAA10g08160 A10 5571827 G A downstream_gene_variant MODIFIER c.*4714G>A| S128
24 BAA10g08160 A10 5571944 C T downstream_gene_variant MODIFIER c.*4831C>T| S270
25 BAA10g08160 A10 5572084 C T downstream_gene_variant MODIFIER c.*4971C>T| S260