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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g30810 A08 20698882 G A missense_variant MODERATE c.329G>A|p.Gly110Asp S241
2 BAA08g30810 A08 20699912 C T splice_region_variant&intron_variant LOW c.765-3C>T| S157
S163
3 BAA08g30810 A08 20700016 C T missense_variant MODERATE c.866C>T|p.Pro289Leu S249
4 BAA08g30810 A08 20700150 C T missense_variant MODERATE c.1000C>T|p.Pro334Ser S43
5 BAA08g30810 A08 20701115 G A missense_variant MODERATE c.1705G>A|p.Asp569Asn S246
6 BAA08g30810 A08 20703289 C T intron_variant MODIFIER c.1899+1980C>T| S173
7 BAA08g30810 A08 20707758 C T missense_variant MODERATE c.2540C>T|p.Pro847Leu S42
8 BAA08g30810 A08 20708350 C T missense_variant MODERATE c.2932C>T|p.Arg978Cys S262
9 BAA08g30810 A08 20708378 G A downstream_gene_variant MODIFIER c.*11G>A| S68
10 BAA08g30810 A08 20708663 G A downstream_gene_variant MODIFIER c.*296G>A| S219
11 BAA08g30810 A08 20709017 G A downstream_gene_variant MODIFIER c.*650G>A| S12
12 BAA08g30810 A08 20712685 C T downstream_gene_variant MODIFIER c.*4318C>T| S270
13 BAA08g30810 A08 20713014 C T downstream_gene_variant MODIFIER c.*4647C>T| S71