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
49901 BAA01g28210 A01 17262303 C T missense_variant MODERATE c.968C>T|p.Ser323Phe S233
49902 BAA01g28210 A01 17262851 G A downstream_gene_variant MODIFIER c.*544G>A| S8
49903 BAA01g28210 A01 17263174 G T downstream_gene_variant MODIFIER c.*867G>T| S39
49904 BAA01g28210 A01 17263451 G A downstream_gene_variant MODIFIER c.*1144G>A| S174
S27
49905 BAA01g28210 A01 17266106 G A downstream_gene_variant MODIFIER c.*3799G>A| S217
S70
49906 BAA01g28210 A01 17266570 C T downstream_gene_variant MODIFIER c.*4263C>T| S233
49907 BAA01g28210 A01 17266778 G A downstream_gene_variant MODIFIER c.*4471G>A| S62
49908 BAA01g28220 A01 17267970 G A downstream_gene_variant MODIFIER c.*4262C>T| S74
49909 BAA01g28220 A01 17268020 C T downstream_gene_variant MODIFIER c.*4212G>A| S266
49910 BAA01g28220 A01 17268025 G A downstream_gene_variant MODIFIER c.*4207C>T| S197
49911 BAA01g28220 A01 17268051 G A downstream_gene_variant MODIFIER c.*4181C>T| S262
49912 BAA01g28220 A01 17268381 C T downstream_gene_variant MODIFIER c.*3851G>A| S256
49913 BAA01g28220 A01 17269585 G A downstream_gene_variant MODIFIER c.*2647C>T| S298
49914 BAA01g28220 A01 17269666 C T downstream_gene_variant MODIFIER c.*2566G>A| S146
49915 BAA01g28220 A01 17269754 C T downstream_gene_variant MODIFIER c.*2478G>A| S18
49916 BAA01g28220 A01 17270422 G A downstream_gene_variant MODIFIER c.*1810C>T| S241
49917 BAA01g28220 A01 17271017 C T downstream_gene_variant MODIFIER c.*1215G>A| S18
49918 BAA01g28220 A01 17271547 C T downstream_gene_variant MODIFIER c.*685G>A| S146
49919 BAA01g28220 A01 17271782 G A downstream_gene_variant MODIFIER c.*450C>T| S94
49920 BAA01g28220 A01 17271985 C T downstream_gene_variant MODIFIER c.*247G>A| S297
49921 BAA01g28220 A01 17272278 G A missense_variant MODERATE c.1304C>T|p.Ala435Val S58
49922 BAA01g28220 A01 17273091 C T synonymous_variant LOW c.825G>A|p.Lys275Lys S136
49923 BAA01g28220 A01 17273279 C T splice_donor_variant&intron_variant HIGH c.768+1G>A| S269
49924 BAA01g28220 A01 17273329 C T missense_variant MODERATE c.719G>A|p.Gly240Asp S77
49925 BAA01g28220 A01 17273369 C T missense_variant MODERATE c.679G>A|p.Gly227Arg S277