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
41601 BAA01g26000 A01 14351181 C T upstream_gene_variant MODIFIER c.-4343C>T| S41
41602 BAA01g26000 A01 14352170 T A upstream_gene_variant MODIFIER c.-3354T>A| S165
S211
S227
41603 BAA01g26000 A01 14353031 C T upstream_gene_variant MODIFIER c.-2493C>T| S61
41604 BAA01g26000 A01 14353118 C T upstream_gene_variant MODIFIER c.-2406C>T| S73
S91
41605 BAA01g26000 A01 14355154 G A upstream_gene_variant MODIFIER c.-370G>A| S287
41606 BAA01g26000 A01 14355631 G A synonymous_variant LOW c.108G>A|p.Lys36Lys S6
41607 BAA01g26000 A01 14355872 C T synonymous_variant LOW c.349C>T|p.Leu117Leu S291
41608 BAA01g26000 A01 14356027 G A synonymous_variant LOW c.504G>A|p.Gln168Gln S32
41609 BAA01g26000 A01 14356340 G A intron_variant MODIFIER c.576-40G>A| S186
41610 BAA01g26000 A01 14356426 G A missense_variant MODERATE c.622G>A|p.Gly208Arg S301
S304
41611 BAA01g26000 A01 14356574 C T missense_variant MODERATE c.770C>T|p.Ala257Val S153
41612 BAA01g26000 A01 14356617 G A missense_variant MODERATE c.813G>A|p.Met271Ile S126
41613 BAA01g26000 A01 14357502 G A missense_variant MODERATE c.1204G>A|p.Glu402Lys S109
41614 BAA01g26000 A01 14357956 C T intron_variant MODIFIER c.1556+28C>T| S125
41615 BAA01g26000 A01 14357975 G A intron_variant MODIFIER c.1556+47G>A| S172
41616 BAA01g26000 A01 14358251 C T intron_variant MODIFIER c.1556+323C>T| S107
41617 BAA01g26000 A01 14358686 C T missense_variant MODERATE c.1636C>T|p.Pro546Ser S20
41618 BAA01g26000 A01 14359569 A T intron_variant MODIFIER c.1821+519A>T| S62
41619 BAA01g26000 A01 14360389 G A splice_region_variant&intron_variant LOW c.1963+5G>A| S32
41620 BAA01g26000 A01 14360619 C T missense_variant MODERATE c.2113C>T|p.Leu705Phe S99
41621 BAA01g26000 A01 14361330 G A missense_variant MODERATE c.2725G>A|p.Gly909Ser S60
41622 BAA01g26000 A01 14361444 C T stop_gained HIGH c.2839C>T|p.Gln947* S8
41623 BAA01g26000 A01 14361837 G A missense_variant MODERATE c.3232G>A|p.Glu1078Lys S33
41624 BAA01g26000 A01 14362296 C T missense_variant MODERATE c.3691C>T|p.Pro1231Ser S286
41625 BAA01g26000 A01 14362827 C T downstream_gene_variant MODIFIER c.*511C>T| S203