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
134351 BAA10g20570 A10 18441747 G A synonymous_variant LOW c.855G>A|p.Glu285Glu S151
S263
134352 BAA10g20560 A10 18443118 G A downstream_gene_variant MODIFIER c.*3392G>A| S202
134353 BAA10g20580 A10 18443936 G A upstream_gene_variant MODIFIER c.-4607G>A| S163
134354 BAA10g20580 A10 18444322 C T upstream_gene_variant MODIFIER c.-4221C>T| S168
134355 BAA10g20580 A10 18445223 G A upstream_gene_variant MODIFIER c.-3320G>A| S226
S41
134356 BAA10g20580 A10 18445497 C T upstream_gene_variant MODIFIER c.-3046C>T| S2
134357 BAA10g20580 A10 18445889 C T upstream_gene_variant MODIFIER c.-2654C>T| S70
134358 BAA10g20580 A10 18446764 G A upstream_gene_variant MODIFIER c.-1779G>A| S105
S106
134359 BAA10g20580 A10 18447057 C T upstream_gene_variant MODIFIER c.-1486C>T| S221
134360 BAA10g20580 A10 18448209 G A upstream_gene_variant MODIFIER c.-334G>A| S172
S217
134361 BAA10g20580 A10 18448972 C T missense_variant MODERATE c.302C>T|p.Ser101Phe S46
134362 BAA10g20590 A10 18451879 C T upstream_gene_variant MODIFIER c.-1688C>T| S274
134363 BAA10g20590 A10 18452874 G A upstream_gene_variant MODIFIER c.-693G>A| S162
134364 BAA10g20590 A10 18453626 C T splice_region_variant&intron_variant LOW c.56+4C>T| S117
134365 BAA10g20590 A10 18454027 A C missense_variant MODERATE c.319A>C|p.Thr107Pro S111
S152
S236
S308
S68
134366 BAA10g20590 A10 18454666 G A missense_variant MODERATE c.958G>A|p.Asp320Asn S198
134367 BAA10g20590 A10 18454852 G A missense_variant MODERATE c.1144G>A|p.Glu382Lys S272
134368 BAA10g20590 A10 18455423 C T missense_variant MODERATE c.1628C>T|p.Ser543Phe S204
134369 BAA10g20590 A10 18455486 G A missense_variant MODERATE c.1691G>A|p.Gly564Asp S16
S92
134370 BAA10g20590 A10 18455515 G A missense_variant MODERATE c.1720G>A|p.Asp574Asn S139
134371 BAA10g20590 A10 18455584 G A missense_variant MODERATE c.1789G>A|p.Asp597Asn S35
134372 BAA10g20590 A10 18456381 G A downstream_gene_variant MODIFIER c.*168G>A| S178
134373 BAA10g20590 A10 18456450 G A downstream_gene_variant MODIFIER c.*237G>A| S263
134374 BAA10g20590 A10 18456809 C T downstream_gene_variant MODIFIER c.*596C>T| S10
134375 BAA10g20590 A10 18457702 G A downstream_gene_variant MODIFIER c.*1489G>A| S265