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
153551 BAA02g02010 A02 895432 C T missense_variant MODERATE c.622G>A|p.Val208Ile S117
153552 BAA02g02020 A02 896889 C T upstream_gene_variant MODIFIER c.-1494C>T| S200
153553 BAA02g02010 A02 897777 G A upstream_gene_variant MODIFIER c.-134C>T| S293
153554 BAA02g02020 A02 898491 C T missense_variant MODERATE c.109C>T|p.Pro37Ser S34
153555 BAA02g02010 A02 898563 C T upstream_gene_variant MODIFIER c.-920G>A| S133
153556 BAA02g02010 A02 899042 G A upstream_gene_variant MODIFIER c.-1399C>T| S265
153557 BAA02g02020 A02 899714 G A missense_variant&splice_region_variant MODERATE c.529G>A|p.Val177Ile S169
153558 BAA02g02030 A02 900332 G A missense_variant MODERATE c.712C>T|p.Pro238Ser S168
153559 BAA02g02030 A02 900578 C T synonymous_variant LOW c.588G>A|p.Lys196Lys S80
153560 BAA02g02030 A02 900911 C T missense_variant MODERATE c.332G>A|p.Ser111Asn S15
S3
153561 BAA02g02010 A02 902048 G A upstream_gene_variant MODIFIER c.-4405C>T| S165
153562 BAA02g02010 A02 902530 C T upstream_gene_variant MODIFIER c.-4887G>A| S51
153563 BAA02g02040 A02 903514 C T synonymous_variant LOW c.214C>T|p.Leu72Leu S262
153564 BAA02g02040 A02 903976 G A synonymous_variant LOW c.411G>A|p.Ser137Ser S219
S72
153565 BAA02g02030 A02 904134 C T upstream_gene_variant MODIFIER c.-2309G>A| S263
153566 BAA02g02030 A02 904294 G A upstream_gene_variant MODIFIER c.-2469C>T| S23
153567 BAA02g02030 A02 904519 C T upstream_gene_variant MODIFIER c.-2694G>A| S71
153568 BAA02g02040 A02 904710 C T synonymous_variant LOW c.687C>T|p.Gly229Gly S33
153569 BAA02g02030 A02 904799 G A upstream_gene_variant MODIFIER c.-2974C>T| S225
153570 BAA02g02040 A02 904910 G A missense_variant MODERATE c.772G>A|p.Glu258Lys S176
153571 BAA02g02040 A02 905183 G A missense_variant MODERATE c.808G>A|p.Val270Met S247
153572 BAA02g02040 A02 905205 G A missense_variant MODERATE c.830G>A|p.Arg277His S202
153573 BAA02g02040 A02 905208 C T missense_variant MODERATE c.833C>T|p.Ser278Phe S177
153574 BAA02g02040 A02 905286 G A missense_variant MODERATE c.911G>A|p.Gly304Glu S255
153575 BAA02g02040 A02 906105 G A missense_variant MODERATE c.991G>A|p.Glu331Lys S132
S137
S215