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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
162601 BAA02g09500 A02 4186013 G A missense_variant MODERATE c.1231G>A|p.Ala411Thr S293
162602 BAA02g09510 A02 4187893 C T upstream_gene_variant MODIFIER c.-1138C>T| S6
162603 BAA02g09510 A02 4188906 C T upstream_gene_variant MODIFIER c.-125C>T| S64
162604 BAA02g09520 A02 4191500 G A synonymous_variant LOW c.4300C>T|p.Leu1434Leu S223
162605 BAA02g09520 A02 4192353 C T synonymous_variant LOW c.3900G>A|p.Leu1300Leu S286
162606 BAA02g09520 A02 4192505 G A missense_variant MODERATE c.3853C>T|p.Leu1285Phe S209
162607 BAA02g09510 A02 4193354 G A downstream_gene_variant MODIFIER c.*2855G>A| S133
162608 BAA02g09520 A02 4193442 G A missense_variant MODERATE c.3277C>T|p.Leu1093Phe S188
162609 BAA02g09520 A02 4193755 C T missense_variant MODERATE c.3139G>A|p.Val1047Ile S121
162610 BAA02g09510 A02 4194167 G A downstream_gene_variant MODIFIER c.*3668G>A| S148
S210
S30
S31
162611 BAA02g09520 A02 4194278 G A missense_variant MODERATE c.2879C>T|p.Pro960Leu S34
162612 BAA02g09510 A02 4195205 G A downstream_gene_variant MODIFIER c.*4706G>A| S11
162613 BAA02g09520 A02 4195912 C T intron_variant MODIFIER c.1962+14G>A| S242
162614 BAA02g09520 A02 4196163 C T intron_variant MODIFIER c.1830+74G>A| S245
162615 BAA02g09530 A02 4196761 C T upstream_gene_variant MODIFIER c.-4439C>T| S18
162616 BAA02g09530 A02 4196977 C T upstream_gene_variant MODIFIER c.-4223C>T| S77
162617 BAA02g09530 A02 4197163 G A upstream_gene_variant MODIFIER c.-4037G>A| S298
162618 BAA02g09530 A02 4198540 C T upstream_gene_variant MODIFIER c.-2660C>T| S55
S76
162619 BAA02g09520 A02 4199050 G A missense_variant MODERATE c.407C>T|p.Ala136Val S50
162620 BAA02g09530 A02 4201310 G A synonymous_variant LOW c.111G>A|p.Lys37Lys S168
162621 BAA02g09520 A02 4201549 C T upstream_gene_variant MODIFIER c.-1083G>A| S219
S72
162622 BAA02g09540 A02 4202535 G A missense_variant MODERATE c.697C>T|p.Pro233Ser S148
S30
S31
162623 BAA02g09540 A02 4203356 G A synonymous_variant LOW c.294C>T|p.Val98Val S148
S210
S30
S31
162624 BAA02g09540 A02 4203367 G A missense_variant MODERATE c.283C>T|p.Leu95Phe S187
162625 BAA02g09520 A02 4203690 G A upstream_gene_variant MODIFIER c.-3224C>T| S98