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
15301 BAA01g11780 A01 5484497 C T upstream_gene_variant MODIFIER c.-546G>A| S299
15302 BAA01g11780 A01 5485406 C T upstream_gene_variant MODIFIER c.-1455G>A| S98
15303 BAA01g11780 A01 5486419 G A upstream_gene_variant MODIFIER c.-2468C>T| S153
15304 BAA01g11790 A01 5489569 C T downstream_gene_variant MODIFIER c.*561G>A| S46
15305 BAA01g11790 A01 5489873 C T downstream_gene_variant MODIFIER c.*257G>A| S2
15306 BAA01g11790 A01 5490461 C T synonymous_variant LOW c.930G>A|p.Gln310Gln S17
S19
15307 BAA01g11790 A01 5490473 C T splice_region_variant&synonymous_variant LOW c.918G>A|p.Gly306Gly S148
S210
S30
S31
15308 BAA01g11790 A01 5490496 C T intron_variant MODIFIER c.917-22G>A| S204
15309 BAA01g11790 A01 5490577 G A intron_variant MODIFIER c.917-103C>T| S45
15310 BAA01g11790 A01 5491228 G A missense_variant MODERATE c.698C>T|p.Pro233Leu S257
15311 BAA01g11790 A01 5492203 G A missense_variant MODERATE c.290C>T|p.Ser97Phe S32
15312 BAA01g11790 A01 5492867 G A missense_variant MODERATE c.74C>T|p.Pro25Leu S54
15313 BAA01g11790 A01 5492883 C T missense_variant MODERATE c.58G>A|p.Gly20Arg S46
15314 BAA01g11790 A01 5494706 G A upstream_gene_variant MODIFIER c.-1766C>T| S114
15315 BAA01g11790 A01 5495678 G A upstream_gene_variant MODIFIER c.-2738C>T| S127
15316 BAA01g11790 A01 5496032 C T upstream_gene_variant MODIFIER c.-3092G>A| S36
15317 BAA01g11800 A01 5498063 C T intron_variant MODIFIER c.499-347G>A| S164
15318 BAA01g11800 A01 5499115 G A splice_region_variant&intron_variant LOW c.465-4C>T| S235
15319 BAA01g11800 A01 5500034 C T intron_variant MODIFIER c.377-372G>A| S82
15320 BAA01g11800 A01 5500270 C T intron_variant MODIFIER c.377-608G>A| S219
S72
15321 BAA01g11800 A01 5502863 G A intron_variant MODIFIER c.376+2239C>T| S34
15322 BAA01g11800 A01 5502966 G A intron_variant MODIFIER c.376+2136C>T| S178
15323 BAA01g11800 A01 5505736 G A intron_variant MODIFIER c.293-551C>T| S133
15324 BAA01g11800 A01 5507032 G A intron_variant MODIFIER c.293-1847C>T| S281
15325 BAA01g11800 A01 5509502 G A intron_variant MODIFIER c.292+3664C>T| S184