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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g08070 A10 5413149 G A downstream_gene_variant MODIFIER c.*4699C>T| S125
2 BAA10g08070 A10 5413333 C T downstream_gene_variant MODIFIER c.*4515G>A| S47
3 BAA10g08070 A10 5413387 G A downstream_gene_variant MODIFIER c.*4461C>T| S172
S217
4 BAA10g08070 A10 5413497 C T downstream_gene_variant MODIFIER c.*4351G>A| S114
5 BAA10g08070 A10 5413630 G A downstream_gene_variant MODIFIER c.*4218C>T| S165
6 BAA10g08070 A10 5413833 G A downstream_gene_variant MODIFIER c.*4015C>T| S16
7 BAA10g08070 A10 5415091 G A downstream_gene_variant MODIFIER c.*2757C>T| S291
8 BAA10g08070 A10 5415705 G A downstream_gene_variant MODIFIER c.*2143C>T| S13
9 BAA10g08070 A10 5416031 G A downstream_gene_variant MODIFIER c.*1817C>T| S274
10 BAA10g08070 A10 5416361 G A downstream_gene_variant MODIFIER c.*1487C>T| S295
11 BAA10g08070 A10 5416832 G A downstream_gene_variant MODIFIER c.*1016C>T| S280
12 BAA10g08070 A10 5417080 G A downstream_gene_variant MODIFIER c.*768C>T| S283
13 BAA10g08070 A10 5417622 G A downstream_gene_variant MODIFIER c.*226C>T| S1
S90
14 BAA10g08070 A10 5418158 C T missense_variant MODERATE c.1700G>A|p.Gly567Glu S132
S137
S215
S89
15 BAA10g08070 A10 5418267 C T missense_variant MODERATE c.1591G>A|p.Gly531Arg S142
16 BAA10g08070 A10 5418325 C T stop_gained HIGH c.1533G>A|p.Trp511* S11
17 BAA10g08070 A10 5418577 C T synonymous_variant LOW c.1281G>A|p.Glu427Glu S122
18 BAA10g08070 A10 5418737 G A missense_variant MODERATE c.1121C>T|p.Ser374Phe S245
19 BAA10g08070 A10 5419296 G A missense_variant MODERATE c.562C>T|p.Pro188Ser S158
20 BAA10g08070 A10 5419689 C T missense_variant MODERATE c.247G>A|p.Glu83Lys S12
21 BAA10g08070 A10 5419943 G A upstream_gene_variant MODIFIER c.-8C>T| S15
S3
22 BAA10g08070 A10 5420033 C T upstream_gene_variant MODIFIER c.-98G>A| S196
23 BAA10g08070 A10 5420253 C T upstream_gene_variant MODIFIER c.-318G>A| S6
24 BAA10g08070 A10 5421032 C G upstream_gene_variant MODIFIER c.-1097G>C| S157
S163
S20
S43
25 BAA10g08070 A10 5422079 G A upstream_gene_variant MODIFIER c.-2144C>T| S293