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
131601 BAA10g18830 A10 17497285 G A missense_variant MODERATE c.352G>A|p.Gly118Ser S288
131602 BAA10g18830 A10 17497518 G A synonymous_variant LOW c.585G>A|p.Arg195Arg S223
131603 BAA10g18830 A10 17497635 C T synonymous_variant LOW c.702C>T|p.Ile234Ile S110
131604 BAA10g18830 A10 17497820 G A missense_variant MODERATE c.887G>A|p.Arg296Lys S62
131605 BAA10g18830 A10 17498678 C T missense_variant MODERATE c.1600C>T|p.Leu534Phe S275
131606 BAA10g18840 A10 17499646 C T synonymous_variant LOW c.1194G>A|p.Glu398Glu S193
131607 BAA10g18840 A10 17500714 C T missense_variant MODERATE c.739G>A|p.Val247Met S25
131608 BAA10g18850 A10 17501255 C T upstream_gene_variant MODIFIER c.-3173C>T| S230
S33
131609 BAA10g18850 A10 17501453 C T upstream_gene_variant MODIFIER c.-2975C>T| S44
131610 BAA10g18850 A10 17501814 C T upstream_gene_variant MODIFIER c.-2614C>T| S247
131611 BAA10g18850 A10 17501817 G A upstream_gene_variant MODIFIER c.-2611G>A| S63
131612 BAA10g18840 A10 17502334 G A missense_variant MODERATE c.149C>T|p.Ser50Phe S240
131613 BAA10g18840 A10 17503202 G A upstream_gene_variant MODIFIER c.-720C>T| S250
131614 BAA10g18840 A10 17503216 G A upstream_gene_variant MODIFIER c.-734C>T| S295
131615 BAA10g18840 A10 17503917 G A upstream_gene_variant MODIFIER c.-1435C>T| S236
131616 BAA10g18840 A10 17504019 G A upstream_gene_variant MODIFIER c.-1537C>T| S205
131617 BAA10g18850 A10 17504434 G A missense_variant MODERATE c.7G>A|p.Ala3Thr S112
131618 BAA10g18850 A10 17504622 C T synonymous_variant LOW c.195C>T|p.His65His S200
131619 BAA10g18850 A10 17504786 T C missense_variant MODERATE c.359T>C|p.Val120Ala S182
131620 BAA10g18850 A10 17505076 G A missense_variant MODERATE c.649G>A|p.Asp217Asn S295
131621 BAA10g18860 A10 17506674 G A synonymous_variant LOW c.2022C>T|p.Ile674Ile S4
131622 BAA10g18860 A10 17507512 C T synonymous_variant LOW c.1269G>A|p.Lys423Lys S249
131623 BAA10g18860 A10 17507679 G A missense_variant MODERATE c.1102C>T|p.Leu368Phe S195
131624 BAA10g18860 A10 17507908 C T missense_variant MODERATE c.947G>A|p.Arg316Lys S95
131625 BAA10g18860 A10 17508599 G A missense_variant MODERATE c.523C>T|p.His175Tyr S132
S137
S215