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
165501 BAA02g11670 A02 5280147 C T upstream_gene_variant MODIFIER c.-4392G>A| S268
165502 BAA02g11680 A02 5280737 G A synonymous_variant LOW c.855C>T|p.Ile285Ile S190
165503 BAA02g11680 A02 5281030 C T synonymous_variant LOW c.648G>A|p.Arg216Arg S182
165504 BAA02g11680 A02 5281675 C T missense_variant MODERATE c.149G>A|p.Arg50Lys S230
165505 BAA02g11680 A02 5282592 G A upstream_gene_variant MODIFIER c.-651C>T| S136
165506 BAA02g11680 A02 5282793 G A upstream_gene_variant MODIFIER c.-852C>T| S4
165507 BAA02g11690 A02 5283642 C T missense_variant MODERATE c.2929G>A|p.Asp977Asn S13
165508 BAA02g11690 A02 5283802 G A missense_variant MODERATE c.2867C>T|p.Ala956Val S286
165509 BAA02g11690 A02 5283816 C T synonymous_variant LOW c.2853G>A|p.Glu951Glu S115
165510 BAA02g11690 A02 5284077 C T missense_variant MODERATE c.2678G>A|p.Arg893His S199
165511 BAA02g11690 A02 5287193 C T intron_variant MODIFIER c.2515-2873G>A| S206
165512 BAA02g11690 A02 5291764 C T missense_variant MODERATE c.2411G>A|p.Gly804Glu S55
165513 BAA02g11690 A02 5293389 G A missense_variant MODERATE c.1369C>T|p.Leu457Phe S205
165514 BAA02g11690 A02 5299178 C T upstream_gene_variant MODIFIER c.-2832G>A| S103
165515 BAA02g11700 A02 5303441 C T missense_variant MODERATE c.1735G>A|p.Val579Met S255
165516 BAA02g11700 A02 5303614 C T missense_variant MODERATE c.1562G>A|p.Arg521Lys S165
165517 BAA02g11700 A02 5303738 G A missense_variant MODERATE c.1438C>T|p.Pro480Ser S298
165518 BAA02g11700 A02 5303759 G A synonymous_variant LOW c.1417C>T|p.Leu473Leu S158
165519 BAA02g11710 A02 5304140 G A upstream_gene_variant MODIFIER c.-4374G>A| S294
165520 BAA02g11710 A02 5304555 G A upstream_gene_variant MODIFIER c.-3959G>A| S17
165521 BAA02g11700 A02 5307438 G A missense_variant MODERATE c.413C>T|p.Thr138Ile S303
165522 BAA02g11700 A02 5308958 C T upstream_gene_variant MODIFIER c.-726G>A| S263
165523 BAA02g11700 A02 5309057 G A upstream_gene_variant MODIFIER c.-825C>T| S161
165524 BAA02g11720 A02 5309585 C T synonymous_variant LOW c.990G>A|p.Leu330Leu S40
S49
165525 BAA02g11720 A02 5309592 C T stop_gained HIGH c.983G>A|p.Trp328* S182