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
74401 BAA01g39110 A01 26024434 C T upstream_gene_variant MODIFIER c.-776G>A| S113
74402 BAA01g39110 A01 26024462 C T upstream_gene_variant MODIFIER c.-804G>A| S157
74403 BAA01g39110 A01 26024959 C T upstream_gene_variant MODIFIER c.-1301G>A| S174
S27
74404 BAA01g39110 A01 26025170 G A upstream_gene_variant MODIFIER c.-1512C>T| S197
74405 BAA01g39110 A01 26025936 G A upstream_gene_variant MODIFIER c.-2278C>T| S175
74406 BAA01g39110 A01 26026049 G A upstream_gene_variant MODIFIER c.-2391C>T| S135
74407 BAA01g39110 A01 26027591 C T upstream_gene_variant MODIFIER c.-3933G>A| S165
74408 BAA01g39120 A01 26029657 C T missense_variant MODERATE c.74C>T|p.Ala25Val S200
74409 BAA01g39140 A01 26029743 G A upstream_gene_variant MODIFIER c.-3740G>A| S109
74410 BAA01g39140 A01 26029882 C T upstream_gene_variant MODIFIER c.-3601C>T| S47
74411 BAA01g39120 A01 26030311 C T synonymous_variant LOW c.291C>T|p.Ile97Ile S16
74412 BAA01g39140 A01 26031008 C T upstream_gene_variant MODIFIER c.-2475C>T| S69
74413 BAA01g39130 A01 26031621 G A synonymous_variant LOW c.361C>T|p.Leu121Leu S271
74414 BAA01g39130 A01 26032696 G A upstream_gene_variant MODIFIER c.-715C>T| S299
74415 BAA01g39130 A01 26033283 G A upstream_gene_variant MODIFIER c.-1302C>T| S252
74416 BAA01g39140 A01 26033623 C T synonymous_variant LOW c.141C>T|p.Phe47Phe S210
S225
74417 BAA01g39140 A01 26033670 C T missense_variant MODERATE c.188C>T|p.Pro63Leu S10
74418 BAA01g39140 A01 26033688 C T missense_variant MODERATE c.206C>T|p.Pro69Leu S135
74419 BAA01g39140 A01 26034087 C T missense_variant MODERATE c.605C>T|p.Thr202Ile S73
S91
74420 BAA01g39130 A01 26034373 C T upstream_gene_variant MODIFIER c.-2392G>A| S148
S30
S31
74421 BAA01g39130 A01 26034573 C T upstream_gene_variant MODIFIER c.-2592G>A| S213
74422 BAA01g39150 A01 26035921 G A missense_variant MODERATE c.227G>A|p.Gly76Glu S36
74423 BAA01g39150 A01 26036251 G A missense_variant MODERATE c.557G>A|p.Gly186Glu S181
74424 BAA01g39150 A01 26037291 C T missense_variant MODERATE c.1597C>T|p.Pro533Ser S16
74425 BAA01g39150 A01 26037399 G A missense_variant MODERATE c.1705G>A|p.Gly569Ser S74