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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g23940 A05 28897143 C T upstream_gene_variant MODIFIER c.-1722C>T| S181
2 BAA05g23940 A05 28897156 C T upstream_gene_variant MODIFIER c.-1709C>T| S207
3 BAA05g23940 A05 28897350 G A upstream_gene_variant MODIFIER c.-1515G>A| S178
4 BAA05g23940 A05 28897504 C T upstream_gene_variant MODIFIER c.-1361C>T| S267
5 BAA05g23940 A05 28897754 C T upstream_gene_variant MODIFIER c.-1111C>T| S183
S198
6 BAA05g23940 A05 28898009 G A upstream_gene_variant MODIFIER c.-856G>A| S184
7 BAA05g23940 A05 28898892 C T missense_variant MODERATE c.28C>T|p.Pro10Ser S208
S93
8 BAA05g23940 A05 28899409 G A missense_variant MODERATE c.388G>A|p.Ala130Thr S107
9 BAA05g23940 A05 28899486 G A synonymous_variant LOW c.465G>A|p.Arg155Arg S136
10 BAA05g23940 A05 28899692 C T missense_variant MODERATE c.671C>T|p.Ser224Phe S305
11 BAA05g23940 A05 28900487 C T missense_variant MODERATE c.1385C>T|p.Ser462Phe S251
12 BAA05g23940 A05 28900559 C T missense_variant MODERATE c.1457C>T|p.Pro486Leu S105
S106
13 BAA05g23940 A05 28901053 G A missense_variant MODERATE c.1951G>A|p.Asp651Asn S80
14 BAA05g23940 A05 28901075 G A missense_variant MODERATE c.1973G>A|p.Ser658Asn S6
15 BAA05g23940 A05 28902106 C T downstream_gene_variant MODIFIER c.*112C>T| S277
16 BAA05g23940 A05 28902232 G A downstream_gene_variant MODIFIER c.*238G>A| S264
17 BAA05g23940 A05 28902305 C T downstream_gene_variant MODIFIER c.*311C>T| S261
18 BAA05g23940 A05 28902555 G A downstream_gene_variant MODIFIER c.*561G>A| S236
19 BAA05g23940 A05 28903040 G A downstream_gene_variant MODIFIER c.*1046G>A| S293
20 BAA05g23940 A05 28903244 C T downstream_gene_variant MODIFIER c.*1250C>T| S12
21 BAA05g23940 A05 28903357 C T downstream_gene_variant MODIFIER c.*1363C>T| S273
22 BAA05g23940 A05 28903936 G A downstream_gene_variant MODIFIER c.*1942G>A| S296
23 BAA05g23940 A05 28904239 C T downstream_gene_variant MODIFIER c.*2245C>T| S251