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
15351 BAA01g11800 A01 5510270 G A intron_variant MODIFIER c.292+2896C>T| S142
15352 BAA01g11800 A01 5510491 G A intron_variant MODIFIER c.292+2675C>T| S191
15353 BAA01g11800 A01 5510537 C T intron_variant MODIFIER c.292+2629G>A| S4
15354 BAA01g11800 A01 5510553 G A intron_variant MODIFIER c.292+2613C>T| S110
15355 BAA01g11800 A01 5510841 C T intron_variant MODIFIER c.292+2325G>A| S112
15356 BAA01g11810 A01 5512471 G A downstream_gene_variant MODIFIER c.*4687C>T| S173
15357 BAA01g11810 A01 5512730 G A downstream_gene_variant MODIFIER c.*4428C>T| S232
15358 BAA01g11800 A01 5513185 G A synonymous_variant LOW c.273C>T|p.Tyr91Tyr S173
15359 BAA01g11800 A01 5513804 G A upstream_gene_variant MODIFIER c.-347C>T| S67
15360 BAA01g11800 A01 5513928 G A upstream_gene_variant MODIFIER c.-471C>T| S105
S106
15361 BAA01g11800 A01 5515512 C T upstream_gene_variant MODIFIER c.-2055G>A| S299
15362 BAA01g11810 A01 5517247 C T missense_variant MODERATE c.331G>A|p.Glu111Lys S46
15363 BAA01g11810 A01 5519370 C T upstream_gene_variant MODIFIER c.-1715G>A| S128
15364 BAA01g11810 A01 5519377 T A upstream_gene_variant MODIFIER c.-1722A>T| S42
15365 BAA01g11810 A01 5519521 C T upstream_gene_variant MODIFIER c.-1866G>A| S80
15366 BAA01g11810 A01 5521213 C T upstream_gene_variant MODIFIER c.-3558G>A| S18
15367 BAA01g11830 A01 5523263 G A downstream_gene_variant MODIFIER c.*3738C>T| S60
15368 BAA01g11830 A01 5523475 C T downstream_gene_variant MODIFIER c.*3526G>A| S287
15369 BAA01g11830 A01 5523831 C T downstream_gene_variant MODIFIER c.*3170G>A| S226
15370 BAA01g11820 A01 5526160 G A synonymous_variant LOW c.1416G>A|p.Glu472Glu S60
15371 BAA01g11820 A01 5526436 G A synonymous_variant LOW c.1692G>A|p.Arg564Arg S235
15372 BAA01g11830 A01 5527336 C T missense_variant MODERATE c.1147G>A|p.Asp383Asn S112
15373 BAA01g11830 A01 5527788 G A missense_variant MODERATE c.695C>T|p.Ala232Val S67
15374 BAA01g11830 A01 5527938 G A missense_variant MODERATE c.545C>T|p.Thr182Met S271
15375 BAA01g11830 A01 5528036 A C missense_variant MODERATE c.447T>G|p.His149Gln S263