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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g29790 A09 20662609 C T upstream_gene_variant MODIFIER c.-3911C>T| S209
2 BAA09g29790 A09 20662682 C T upstream_gene_variant MODIFIER c.-3838C>T| S168
3 BAA09g29790 A09 20662907 G A upstream_gene_variant MODIFIER c.-3613G>A| S303
4 BAA09g29790 A09 20662962 C T upstream_gene_variant MODIFIER c.-3558C>T| S124
5 BAA09g29790 A09 20663205 C T upstream_gene_variant MODIFIER c.-3315C>T| S182
6 BAA09g29790 A09 20663684 C T upstream_gene_variant MODIFIER c.-2836C>T| S200
S303
7 BAA09g29790 A09 20663823 C T upstream_gene_variant MODIFIER c.-2697C>T| S81
8 BAA09g29790 A09 20663836 G A upstream_gene_variant MODIFIER c.-2684G>A| S124
9 BAA09g29790 A09 20663885 C T upstream_gene_variant MODIFIER c.-2635C>T| S40
10 BAA09g29790 A09 20666090 C T upstream_gene_variant MODIFIER c.-430C>T| S63
11 BAA09g29790 A09 20667099 C T synonymous_variant LOW c.138C>T|p.Val46Val S306
S308
12 BAA09g29790 A09 20667110 C T missense_variant MODERATE c.149C>T|p.Thr50Ile S276
13 BAA09g29790 A09 20667773 G A intron_variant MODIFIER c.402-97G>A| S15
S3
14 BAA09g29790 A09 20667969 G A intron_variant MODIFIER c.486+15G>A| S53
15 BAA09g29790 A09 20669554 C T downstream_gene_variant MODIFIER c.*1449C>T| S23
16 BAA09g29790 A09 20670308 C T downstream_gene_variant MODIFIER c.*2203C>T| S209
17 BAA09g29790 A09 20672330 G A downstream_gene_variant MODIFIER c.*4225G>A| S280
18 BAA09g29790 A09 20672758 G A downstream_gene_variant MODIFIER c.*4653G>A| S59