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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g39100 A05 38252641 G A upstream_gene_variant MODIFIER c.-4586G>A| S243
S299
2 BAA05g39100 A05 38253667 G A upstream_gene_variant MODIFIER c.-3560G>A| S76
3 BAA05g39100 A05 38255772 G A upstream_gene_variant MODIFIER c.-1455G>A| S74
4 BAA05g39100 A05 38256972 G A upstream_gene_variant MODIFIER c.-255G>A| S210
S225
5 BAA05g39100 A05 38257373 C T synonymous_variant LOW c.147C>T|p.His49His S37
6 BAA05g39100 A05 38257502 G A missense_variant MODERATE c.203G>A|p.Cys68Tyr S190
7 BAA05g39100 A05 38257711 G A missense_variant MODERATE c.412G>A|p.Gly138Arg S48
8 BAA05g39100 A05 38258492 G A missense_variant MODERATE c.1123G>A|p.Val375Ile S207
9 BAA05g39100 A05 38258507 C T stop_gained HIGH c.1138C>T|p.Gln380* S289
S290
10 BAA05g39100 A05 38258665 C T synonymous_variant LOW c.1296C>T|p.Val432Val S139
11 BAA05g39100 A05 38259317 G A missense_variant MODERATE c.1778G>A|p.Gly593Glu S30
S31
12 BAA05g39100 A05 38259432 G A missense_variant MODERATE c.1893G>A|p.Met631Ile S62
13 BAA05g39100 A05 38259989 C T synonymous_variant LOW c.2301C>T|p.Ser767Ser S65
14 BAA05g39100 A05 38264136 C T downstream_gene_variant MODIFIER c.*3443C>T| S230
15 BAA05g39100 A05 38264553 C T downstream_gene_variant MODIFIER c.*3860C>T| S286
16 BAA05g39100 A05 38264799 G A downstream_gene_variant MODIFIER c.*4106G>A| S23
17 BAA05g39100 A05 38264807 C T downstream_gene_variant MODIFIER c.*4114C>T| S35