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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g19400 A02 10052247 G A upstream_gene_variant MODIFIER c.-888G>A| S276
2 BAA02g19400 A02 10053152 C T synonymous_variant LOW c.18C>T|p.Leu6Leu S6
3 BAA02g19400 A02 10053220 G A missense_variant MODERATE c.86G>A|p.Gly29Glu S293
4 BAA02g19400 A02 10053327 G A intron_variant MODIFIER c.110-12G>A| S62
5 BAA02g19400 A02 10054196 G A intron_variant MODIFIER c.584+43G>A| S13
S140
S168
S279
S64
6 BAA02g19400 A02 10054740 G A missense_variant&splice_region_variant MODERATE c.731G>A|p.Arg244Lys S240
7 BAA02g19400 A02 10055119 C T intron_variant MODIFIER c.800+310C>T| S121
8 BAA02g19400 A02 10055151 G A intron_variant MODIFIER c.800+342G>A| S5
9 BAA02g19400 A02 10055613 G A intron_variant MODIFIER c.801-260G>A| S126
10 BAA02g19400 A02 10056690 C T splice_region_variant&intron_variant LOW c.1083-7C>T| S2
11 BAA02g19400 A02 10056754 C T synonymous_variant LOW c.1140C>T|p.Asn380Asn S80
12 BAA02g19400 A02 10057293 G A intron_variant MODIFIER c.1149-286G>A| S116
13 BAA02g19400 A02 10060092 G A intron_variant MODIFIER c.2088+1157G>A| S303
14 BAA02g19400 A02 10061514 T C intron_variant MODIFIER c.2089-146T>C| S50
15 BAA02g19400 A02 10061980 G A missense_variant MODERATE c.2311G>A|p.Asp771Asn S229