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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g15620 A05 8340987 C T downstream_gene_variant MODIFIER c.*3252G>A| S195
2 BAA05g15620 A05 8341178 C T downstream_gene_variant MODIFIER c.*3061G>A| S198
3 BAA05g15620 A05 8341348 C T downstream_gene_variant MODIFIER c.*2891G>A| S99
4 BAA05g15620 A05 8342148 C T downstream_gene_variant MODIFIER c.*2091G>A| S206
S26
5 BAA05g15620 A05 8342208 C T downstream_gene_variant MODIFIER c.*2031G>A| S63
6 BAA05g15620 A05 8342247 G A downstream_gene_variant MODIFIER c.*1992C>T| S260
7 BAA05g15620 A05 8342960 C T downstream_gene_variant MODIFIER c.*1279G>A| S126
8 BAA05g15620 A05 8343024 C T downstream_gene_variant MODIFIER c.*1215G>A| S15
9 BAA05g15620 A05 8343271 C T downstream_gene_variant MODIFIER c.*968G>A| S119
10 BAA05g15620 A05 8343346 C T downstream_gene_variant MODIFIER c.*893G>A| S180
11 BAA05g15620 A05 8344124 C T downstream_gene_variant MODIFIER c.*115G>A| S176
12 BAA05g15620 A05 8344527 G A synonymous_variant LOW c.1644C>T|p.Ala548Ala S221
13 BAA05g15620 A05 8345174 C T splice_acceptor_variant&intron_variant HIGH c.998-1G>A| S295
14 BAA05g15620 A05 8346472 C T synonymous_variant LOW c.972G>A|p.Arg324Arg S99
15 BAA05g15620 A05 8346769 G A synonymous_variant LOW c.675C>T|p.Ser225Ser S172
S217
16 BAA05g15620 A05 8347728 G A missense_variant MODERATE c.26C>T|p.Thr9Ile S217
17 BAA05g15620 A05 8347799 G A upstream_gene_variant MODIFIER c.-46C>T| S226
18 BAA05g15620 A05 8348086 C T upstream_gene_variant MODIFIER c.-333G>A| S9
19 BAA05g15620 A05 8348092 C T upstream_gene_variant MODIFIER c.-339G>A| S73
S91