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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g65600 A09 60357789 G A upstream_gene_variant MODIFIER c.-4393G>A| S255
2 BAA09g65600 A09 60357984 G A upstream_gene_variant MODIFIER c.-4198G>A| S297
3 BAA09g65600 A09 60358998 C T upstream_gene_variant MODIFIER c.-3184C>T| S119
4 BAA09g65600 A09 60359039 C T upstream_gene_variant MODIFIER c.-3143C>T| S292
5 BAA09g65600 A09 60362515 G A missense_variant MODERATE c.334G>A|p.Gly112Arg S98
6 BAA09g65600 A09 60362534 C T missense_variant MODERATE c.353C>T|p.Thr118Ile S173
7 BAA09g65600 A09 60363559 G A missense_variant MODERATE c.1378G>A|p.Glu460Lys S238
8 BAA09g65600 A09 60363635 C T missense_variant MODERATE c.1454C>T|p.Ala485Val S56
9 BAA09g65600 A09 60363768 C T synonymous_variant LOW c.1587C>T|p.Thr529Thr S168
10 BAA09g65600 A09 60364155 G A missense_variant MODERATE c.1974G>A|p.Met658Ile S79
S84
11 BAA09g65600 A09 60364267 C T missense_variant MODERATE c.2086C>T|p.Arg696Cys S161
S228
S289
S290
12 BAA09g65600 A09 60364936 G A missense_variant MODERATE c.2755G>A|p.Gly919Arg S189
13 BAA09g65600 A09 60365439 C T splice_region_variant&intron_variant LOW c.3251+7C>T| S224
14 BAA09g65600 A09 60367414 G A downstream_gene_variant MODIFIER c.*1819G>A| S65
15 BAA09g65600 A09 60367475 C T downstream_gene_variant MODIFIER c.*1880C>T| S257