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
173051 BAA02g16610 A02 8144831 C T synonymous_variant LOW c.4986G>A|p.Arg1662Arg S202
173052 BAA02g16610 A02 8145946 C T intron_variant MODIFIER c.4019-148G>A| S208
S219
173053 BAA02g16610 A02 8146613 G A intron_variant MODIFIER c.4019-815C>T| S62
173054 BAA02g16610 A02 8148170 G A intron_variant MODIFIER c.4019-2372C>T| S13
S168
S279
S64
173055 BAA02g16610 A02 8148368 G A intron_variant MODIFIER c.4019-2570C>T| S139
173056 BAA02g16610 A02 8148513 C T intron_variant MODIFIER c.4019-2715G>A| S128
173057 BAA02g16610 A02 8151162 C T intron_variant MODIFIER c.4019-5364G>A| S65
173058 BAA02g16610 A02 8151479 C T intron_variant MODIFIER c.4018+5327G>A| S112
173059 BAA02g16610 A02 8153980 C T intron_variant MODIFIER c.4018+2826G>A| S39
173060 BAA02g16610 A02 8154585 G A intron_variant MODIFIER c.4018+2221C>T| S60
173061 BAA02g16610 A02 8156117 C T intron_variant MODIFIER c.4018+689G>A| S267
173062 BAA02g16610 A02 8159589 G A intron_variant MODIFIER c.3573-1615C>T| S37
173063 BAA02g16610 A02 8160014 C T intron_variant MODIFIER c.3572+1631G>A| S200
173064 BAA02g16610 A02 8160108 C T intron_variant MODIFIER c.3572+1537G>A| S180
173065 BAA02g16610 A02 8160538 C T intron_variant MODIFIER c.3572+1107G>A| S78
173066 BAA02g16610 A02 8160659 C T intron_variant MODIFIER c.3572+986G>A| S55
173067 BAA02g16610 A02 8161234 C T intron_variant MODIFIER c.3572+411G>A| S276
173068 BAA02g16610 A02 8161492 C T intron_variant MODIFIER c.3572+153G>A| S183
S198
173069 BAA02g16610 A02 8161535 C T intron_variant MODIFIER c.3572+110G>A| S63
173070 BAA02g16610 A02 8162198 G A intron_variant MODIFIER c.3463+169C>T| S57
173071 BAA02g16610 A02 8162326 C T intron_variant MODIFIER c.3463+41G>A| S130
173072 BAA02g16610 A02 8162382 C T missense_variant MODERATE c.3448G>A|p.Gly1150Arg S249
173073 BAA02g16610 A02 8162732 C T intron_variant MODIFIER c.3346-248G>A| S263
173074 BAA02g16610 A02 8163123 C T intron_variant MODIFIER c.3345+133G>A| S299
173075 BAA02g16610 A02 8163863 G A intron_variant MODIFIER c.2869+47C>T| S122