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
40601 BAA01g25730 A01 14017273 C T upstream_gene_variant MODIFIER c.-2016C>T| S203
40602 BAA01g25730 A01 14018030 C G upstream_gene_variant MODIFIER c.-1259C>G| S196
40603 BAA01g25730 A01 14018950 C T upstream_gene_variant MODIFIER c.-339C>T| S251
40604 BAA01g25730 A01 14019286 C T upstream_gene_variant MODIFIER c.-3C>T| S176
40605 BAA01g25730 A01 14019582 G A synonymous_variant LOW c.138G>A|p.Gln46Gln S15
S3
40606 BAA01g25730 A01 14019695 G A missense_variant MODERATE c.251G>A|p.Cys84Tyr S110
40607 BAA01g25730 A01 14019707 C T missense_variant MODERATE c.263C>T|p.Ser88Phe S28
S294
40608 BAA01g25740 A01 14020354 C T upstream_gene_variant MODIFIER c.-2882C>T| S46
40609 BAA01g25740 A01 14021182 C T upstream_gene_variant MODIFIER c.-2054C>T| S158
40610 BAA01g25740 A01 14022425 G A upstream_gene_variant MODIFIER c.-811G>A| S59
40611 BAA01g25740 A01 14023437 C T splice_region_variant&intron_variant LOW c.53-4C>T| S155
S211
40612 BAA01g25750 A01 14023580 G A upstream_gene_variant MODIFIER c.-4219G>A| S186
40613 BAA01g25740 A01 14023812 C T synonymous_variant LOW c.285C>T|p.Ala95Ala S25
S264
40614 BAA01g25740 A01 14023949 G A missense_variant MODERATE c.338G>A|p.Gly113Glu S92
40615 BAA01g25750 A01 14024874 G A upstream_gene_variant MODIFIER c.-2925G>A| S201
40616 BAA01g25750 A01 14024890 G A upstream_gene_variant MODIFIER c.-2909G>A| S191
40617 BAA01g25740 A01 14025898 C T missense_variant MODERATE c.758C>T|p.Ala253Val S233
40618 BAA01g25750 A01 14026607 C T upstream_gene_variant MODIFIER c.-1192C>T| S136
40619 BAA01g25750 A01 14026782 G A upstream_gene_variant MODIFIER c.-1017G>A| S202
40620 BAA01g25750 A01 14027032 G A upstream_gene_variant MODIFIER c.-767G>A| S37
40621 BAA01g25750 A01 14027808 C T missense_variant MODERATE c.10C>T|p.Leu4Phe S48
40622 BAA01g25760 A01 14029451 C T upstream_gene_variant MODIFIER c.-4812C>T| S210
40623 BAA01g25760 A01 14029644 G A upstream_gene_variant MODIFIER c.-4619G>A| S281
40624 BAA01g25760 A01 14030648 G A upstream_gene_variant MODIFIER c.-3615G>A| S197
40625 BAA01g25760 A01 14031342 G A upstream_gene_variant MODIFIER c.-2921G>A| S74