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 BAA02g29380 A02 16815680 C T missense_variant MODERATE c.2095G>A|p.Gly699Arg S105
S106
2 BAA02g29380 A02 16816347 C T missense_variant MODERATE c.1760G>A|p.Gly587Glu S9
3 BAA02g29380 A02 16818787 C T splice_donor_variant&intron_variant HIGH c.1512+1G>A| S266
4 BAA02g29380 A02 16818813 G A missense_variant MODERATE c.1487C>T|p.Thr496Ile S207
5 BAA02g29380 A02 16818881 G A synonymous_variant LOW c.1419C>T|p.Asp473Asp S184
6 BAA02g29380 A02 16818905 C T synonymous_variant LOW c.1395G>A|p.Lys465Lys S140
7 BAA02g29380 A02 16819619 G A splice_region_variant&synonymous_variant LOW c.1152C>T|p.Leu384Leu S297
8 BAA02g29380 A02 16820319 G A missense_variant MODERATE c.700C>T|p.Pro234Ser S188
9 BAA02g29380 A02 16820606 G A missense_variant MODERATE c.500C>T|p.Ser167Phe S225
10 BAA02g29380 A02 16821346 G A synonymous_variant LOW c.123C>T|p.Leu41Leu S28
S30
11 BAA02g29380 A02 16822666 G A upstream_gene_variant MODIFIER c.-1198C>T| S265
12 BAA02g29380 A02 16824833 C T upstream_gene_variant MODIFIER c.-3365G>A| S185
13 BAA02g29380 A02 16825456 C T upstream_gene_variant MODIFIER c.-3988G>A| S79
S84
14 BAA02g29380 A02 16825459 C T upstream_gene_variant MODIFIER c.-3991G>A| S66
15 BAA02g29380 A02 16825768 C T upstream_gene_variant MODIFIER c.-4300G>A| S82
S92
16 BAA02g29380 A02 16826386 C T upstream_gene_variant MODIFIER c.-4918G>A| S239