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 BAA10g07090 A10 3946722 C T upstream_gene_variant MODIFIER c.-4924C>T| S162
S225
2 BAA10g07090 A10 3947444 G A upstream_gene_variant MODIFIER c.-4202G>A| S198
3 BAA10g07090 A10 3947585 C T upstream_gene_variant MODIFIER c.-4061C>T| S41
4 BAA10g07090 A10 3948481 G A upstream_gene_variant MODIFIER c.-3165G>A| S103
5 BAA10g07090 A10 3948493 C T upstream_gene_variant MODIFIER c.-3153C>T| S259
6 BAA10g07090 A10 3948506 C T upstream_gene_variant MODIFIER c.-3140C>T| S6
7 BAA10g07090 A10 3948511 G A upstream_gene_variant MODIFIER c.-3135G>A| S17
8 BAA10g07090 A10 3948743 G A upstream_gene_variant MODIFIER c.-2903G>A| S262
9 BAA10g07090 A10 3948793 C T upstream_gene_variant MODIFIER c.-2853C>T| S206
S26
10 BAA10g07090 A10 3949564 G A upstream_gene_variant MODIFIER c.-2082G>A| S69
11 BAA10g07090 A10 3950216 C T upstream_gene_variant MODIFIER c.-1430C>T| S114
12 BAA10g07090 A10 3950918 C T upstream_gene_variant MODIFIER c.-728C>T| S54
13 BAA10g07090 A10 3951168 C T upstream_gene_variant MODIFIER c.-478C>T| S25
14 BAA10g07090 A10 3951603 C T upstream_gene_variant MODIFIER c.-43C>T| S96
15 BAA10g07090 A10 3951683 G A missense_variant MODERATE c.38G>A|p.Gly13Glu S207
16 BAA10g07090 A10 3951740 C T missense_variant MODERATE c.95C>T|p.Ser32Phe S282
17 BAA10g07090 A10 3952268 G A intron_variant MODIFIER c.360+263G>A| S20
18 BAA10g07090 A10 3952421 C T intron_variant MODIFIER c.361-285C>T| S249
19 BAA10g07090 A10 3952498 C T intron_variant MODIFIER c.361-208C>T| S180
20 BAA10g07090 A10 3952500 C T intron_variant MODIFIER c.361-206C>T| S161
21 BAA10g07090 A10 3952750 G A stop_gained HIGH c.405G>A|p.Trp135* S14
22 BAA10g07090 A10 3952795 C T synonymous_variant LOW c.450C>T|p.Cys150Cys S155
S172
S211
23 BAA10g07090 A10 3952925 G A downstream_gene_variant MODIFIER c.*58G>A| S236
24 BAA10g07090 A10 3953583 C T downstream_gene_variant MODIFIER c.*716C>T| S188