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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g44060 A01 29138787 C T upstream_gene_variant MODIFIER c.-4140C>T| S23
2 BAA01g44060 A01 29139828 G A upstream_gene_variant MODIFIER c.-3099G>A| S202
3 BAA01g44060 A01 29140008 G A upstream_gene_variant MODIFIER c.-2919G>A| S33
4 BAA01g44060 A01 29142281 C T upstream_gene_variant MODIFIER c.-646C>T| S58
5 BAA01g44060 A01 29142469 C T upstream_gene_variant MODIFIER c.-458C>T| S19
6 BAA01g44060 A01 29142595 C T upstream_gene_variant MODIFIER c.-332C>T| S19
7 BAA01g44060 A01 29142636 C T upstream_gene_variant MODIFIER c.-291C>T| S233
8 BAA01g44060 A01 29143775 C T intron_variant MODIFIER c.666+21C>T| S51
9 BAA01g44060 A01 29143890 G A missense_variant MODERATE c.736G>A|p.Glu246Lys S272
10 BAA01g44060 A01 29144911 G A missense_variant MODERATE c.1129G>A|p.Asp377Asn S53
11 BAA01g44060 A01 29145665 C T missense_variant MODERATE c.1577C>T|p.Ala526Val S103
12 BAA01g44060 A01 29145895 C T synonymous_variant LOW c.1710C>T|p.Phe570Phe S11
13 BAA01g44060 A01 29147763 A G downstream_gene_variant MODIFIER c.*1555A>G| S59
14 BAA01g44060 A01 29149170 C T downstream_gene_variant MODIFIER c.*2962C>T| S206
S26
15 BAA01g44060 A01 29149894 C T downstream_gene_variant MODIFIER c.*3686C>T| S200
16 BAA01g44060 A01 29149952 C T downstream_gene_variant MODIFIER c.*3744C>T| S8