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
75601 BAA01g39810 A01 26442942 C T synonymous_variant LOW c.333C>T|p.Leu111Leu S289
S290
75602 BAA01g39810 A01 26443065 C T synonymous_variant LOW c.456C>T|p.Arg152Arg S182
75603 BAA01g39810 A01 26443101 C T synonymous_variant LOW c.492C>T|p.Thr164Thr S64
75604 BAA01g39810 A01 26443140 C T synonymous_variant LOW c.531C>T|p.Leu177Leu S56
75605 BAA01g39810 A01 26443183 G A missense_variant MODERATE c.574G>A|p.Glu192Lys S104
75606 BAA01g39820 A01 26443400 G A upstream_gene_variant MODIFIER c.-1524G>A| S66
75607 BAA01g39810 A01 26443682 G A synonymous_variant LOW c.717G>A|p.Arg239Arg S217
75608 BAA01g39820 A01 26445113 C T missense_variant MODERATE c.190C>T|p.Pro64Ser S80
75609 BAA01g39810 A01 26445429 G A downstream_gene_variant MODIFIER c.*1225G>A| S263
75610 BAA01g39810 A01 26445518 G A downstream_gene_variant MODIFIER c.*1314G>A| S238
75611 BAA01g39810 A01 26446348 G A downstream_gene_variant MODIFIER c.*2144G>A| S262
75612 BAA01g39810 A01 26447845 C T downstream_gene_variant MODIFIER c.*3641C>T| S115
75613 BAA01g39820 A01 26449528 C T downstream_gene_variant MODIFIER c.*4389C>T| S94
75614 BAA01g39830 A01 26450451 C T downstream_gene_variant MODIFIER c.*3042G>A| S134
75615 BAA01g39830 A01 26451153 G A downstream_gene_variant MODIFIER c.*2340C>T| S218
75616 BAA01g39830 A01 26452248 C T downstream_gene_variant MODIFIER c.*1245G>A| S261
75617 BAA01g39830 A01 26453534 C T missense_variant MODERATE c.853G>A|p.Glu285Lys S64
75618 BAA01g39830 A01 26454033 C T intron_variant MODIFIER c.823-469G>A| S16
75619 BAA01g39830 A01 26454166 G A intron_variant MODIFIER c.823-602C>T| S296
75620 BAA01g39830 A01 26454536 C T intron_variant MODIFIER c.822+730G>A| S192
S286
75621 BAA01g39830 A01 26454585 C T intron_variant MODIFIER c.822+681G>A| S279
75622 BAA01g39830 A01 26454672 C T intron_variant MODIFIER c.822+594G>A| S19
75623 BAA01g39830 A01 26454953 C T intron_variant MODIFIER c.822+313G>A| S275
75624 BAA01g39830 A01 26455065 C T intron_variant MODIFIER c.822+201G>A| S301
S304
75625 BAA01g39830 A01 26455464 G A synonymous_variant LOW c.624C>T|p.Arg208Arg S9