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
44901 BAA01g27070 A01 15417453 C T upstream_gene_variant MODIFIER c.-741C>T| S303
44902 BAA01g27070 A01 15417608 C T upstream_gene_variant MODIFIER c.-586C>T| S289
S290
44903 BAA01g27070 A01 15418344 G A missense_variant&splice_region_variant MODERATE c.151G>A|p.Glu51Lys S180
44904 BAA01g27070 A01 15418398 C T missense_variant MODERATE c.169C>T|p.Leu57Phe S150
44905 BAA01g27070 A01 15419360 C T downstream_gene_variant MODIFIER c.*744C>T| S38
44906 BAA01g27080 A01 15420085 C T upstream_gene_variant MODIFIER c.-4985C>T| S36
44907 BAA01g27080 A01 15420141 C T upstream_gene_variant MODIFIER c.-4929C>T| S272
44908 BAA01g27080 A01 15420319 C T upstream_gene_variant MODIFIER c.-4751C>T| S295
44909 BAA01g27080 A01 15420487 G A upstream_gene_variant MODIFIER c.-4583G>A| S283
44910 BAA01g27080 A01 15421109 C T upstream_gene_variant MODIFIER c.-3961C>T| S293
44911 BAA01g27080 A01 15421449 C T upstream_gene_variant MODIFIER c.-3621C>T| S213
44912 BAA01g27080 A01 15422532 C T upstream_gene_variant MODIFIER c.-2538C>T| S303
44913 BAA01g27080 A01 15422721 C T upstream_gene_variant MODIFIER c.-2349C>T| S279
44914 BAA01g27080 A01 15423216 C T upstream_gene_variant MODIFIER c.-1854C>T| S221
44915 BAA01g27080 A01 15423560 C T upstream_gene_variant MODIFIER c.-1510C>T| S20
44916 BAA01g27080 A01 15423599 C T upstream_gene_variant MODIFIER c.-1471C>T| S110
S53
44917 BAA01g27080 A01 15423843 C T upstream_gene_variant MODIFIER c.-1227C>T| S294
44918 BAA01g27080 A01 15423957 G A upstream_gene_variant MODIFIER c.-1113G>A| S308
44919 BAA01g27080 A01 15424155 C T upstream_gene_variant MODIFIER c.-915C>T| S185
44920 BAA01g27080 A01 15425094 G A missense_variant MODERATE c.25G>A|p.Glu9Lys S278
44921 BAA01g27080 A01 15425128 G A missense_variant MODERATE c.59G>A|p.Gly20Glu S280
44922 BAA01g27080 A01 15425310 A T synonymous_variant LOW c.123A>T|p.Val41Val S56
44923 BAA01g27080 A01 15425459 C T intron_variant MODIFIER c.127-85C>T| S210
S225
44924 BAA01g27080 A01 15426025 G A intron_variant MODIFIER c.304-45G>A| S70
44925 BAA01g27080 A01 15426702 C T intron_variant MODIFIER c.608-163C>T| S286