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
51701 BAA01g28600 A01 17928389 C T intron_variant MODIFIER c.3103+31C>T| S293
51702 BAA01g28600 A01 17928772 C T missense_variant MODERATE c.3350C>T|p.Ser1117Phe S284
51703 BAA01g28600 A01 17928777 G A missense_variant&splice_region_variant MODERATE c.3355G>A|p.Glu1119Lys S241
51704 BAA01g28600 A01 17929499 C T downstream_gene_variant MODIFIER c.*389C>T| S32
51705 BAA01g28600 A01 17929830 G A downstream_gene_variant MODIFIER c.*720G>A| S163
51706 BAA01g28600 A01 17929994 C T downstream_gene_variant MODIFIER c.*884C>T| S35
51707 BAA01g28600 A01 17930146 G A downstream_gene_variant MODIFIER c.*1036G>A| S280
51708 BAA01g28600 A01 17930255 G A downstream_gene_variant MODIFIER c.*1145G>A| S288
51709 BAA01g28600 A01 17930795 G A downstream_gene_variant MODIFIER c.*1685G>A| S61
51710 BAA01g28600 A01 17930859 G A downstream_gene_variant MODIFIER c.*1749G>A| S75
51711 BAA01g28610 A01 17933309 C T upstream_gene_variant MODIFIER c.-4735C>T| S48
51712 BAA01g28610 A01 17933882 G A upstream_gene_variant MODIFIER c.-4162G>A| S151
51713 BAA01g28610 A01 17934146 G A upstream_gene_variant MODIFIER c.-3898G>A| S116
51714 BAA01g28610 A01 17935599 C T upstream_gene_variant MODIFIER c.-2445C>T| S233
51715 BAA01g28610 A01 17935632 C T upstream_gene_variant MODIFIER c.-2412C>T| S108
51716 BAA01g28610 A01 17935659 C T upstream_gene_variant MODIFIER c.-2385C>T| S10
51717 BAA01g28610 A01 17935698 G A upstream_gene_variant MODIFIER c.-2346G>A| S6
51718 BAA01g28610 A01 17936229 A T upstream_gene_variant MODIFIER c.-1815A>T| S250
51719 BAA01g28610 A01 17936913 G A upstream_gene_variant MODIFIER c.-1131G>A| S278
51720 BAA01g28610 A01 17938549 C T intron_variant MODIFIER c.372+43C>T| S255
51721 BAA01g28610 A01 17938861 C T missense_variant MODERATE c.500C>T|p.Ser167Phe S148
51722 BAA01g28610 A01 17939374 C T intron_variant MODIFIER c.792+19C>T| S118
51723 BAA01g28610 A01 17939858 G A missense_variant MODERATE c.1075G>A|p.Val359Ile S292
51724 BAA01g28610 A01 17939937 G A intron_variant MODIFIER c.1108-29G>A| S140
51725 BAA01g28610 A01 17940275 T A intron_variant MODIFIER c.1246-96T>A| S79
S84