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 BAA08g16800 A08 13805205 T C upstream_gene_variant MODIFIER c.-4913T>C| S5
2 BAA08g16800 A08 13805582 G A upstream_gene_variant MODIFIER c.-4536G>A| S267
3 BAA08g16800 A08 13805955 T A upstream_gene_variant MODIFIER c.-4163T>A| S26
4 BAA08g16800 A08 13806539 C T upstream_gene_variant MODIFIER c.-3579C>T| S88
5 BAA08g16800 A08 13806798 C T upstream_gene_variant MODIFIER c.-3320C>T| S168
6 BAA08g16800 A08 13806965 C T upstream_gene_variant MODIFIER c.-3153C>T| S60
7 BAA08g16800 A08 13806999 C T upstream_gene_variant MODIFIER c.-3119C>T| S301
S304
8 BAA08g16800 A08 13808184 C T upstream_gene_variant MODIFIER c.-1934C>T| S126
9 BAA08g16800 A08 13810739 G A missense_variant MODERATE c.335G>A|p.Gly112Glu S16
10 BAA08g16800 A08 13810963 G A missense_variant MODERATE c.458G>A|p.Gly153Glu S155
S211
11 BAA08g16800 A08 13811127 G A missense_variant MODERATE c.532G>A|p.Asp178Asn S5
12 BAA08g16800 A08 13811133 C T missense_variant MODERATE c.538C>T|p.Pro180Ser S177
13 BAA08g16800 A08 13812625 G A missense_variant MODERATE c.1276G>A|p.Asp426Asn S107
14 BAA08g16800 A08 13813221 C T missense_variant MODERATE c.1781C>T|p.Thr594Ile S38
15 BAA08g16800 A08 13814111 C T downstream_gene_variant MODIFIER c.*826C>T| S236
S260
16 BAA08g16800 A08 13814329 C T downstream_gene_variant MODIFIER c.*1044C>T| S259
17 BAA08g16800 A08 13814383 G A downstream_gene_variant MODIFIER c.*1098G>A| S14