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
29351 BAA01g20700 A01 10219005 G A upstream_gene_variant MODIFIER c.-4663G>A| S144
29352 BAA01g20690 A01 10219508 C T synonymous_variant LOW c.1608G>A|p.Glu536Glu S135
S185
S203
29353 BAA01g20700 A01 10219598 C T upstream_gene_variant MODIFIER c.-4070C>T| S139
29354 BAA01g20690 A01 10219882 G A synonymous_variant LOW c.1440C>T|p.Leu480Leu S202
29355 BAA01g20690 A01 10220583 C T splice_acceptor_variant&intron_variant HIGH c.1033-1G>A| S42
29356 BAA01g20700 A01 10220618 A C upstream_gene_variant MODIFIER c.-3050A>C| S121
S158
S18
S85
29357 BAA01g20690 A01 10220838 C T missense_variant&splice_region_variant MODERATE c.961G>A|p.Asp321Asn S200
29358 BAA01g20690 A01 10221995 C T missense_variant MODERATE c.313G>A|p.Gly105Arg S143
29359 BAA01g20690 A01 10222556 T A upstream_gene_variant MODIFIER c.-249A>T| S1
S90
29360 BAA01g20690 A01 10222615 C T upstream_gene_variant MODIFIER c.-308G>A| S130
29361 BAA01g20690 A01 10223130 C T upstream_gene_variant MODIFIER c.-823G>A| S270
29362 BAA01g20690 A01 10223333 G A upstream_gene_variant MODIFIER c.-1026C>T| S211
S227
29363 BAA01g20700 A01 10224248 C T missense_variant MODERATE c.581C>T|p.Ser194Phe S18
29364 BAA01g20700 A01 10224394 G A missense_variant MODERATE c.659G>A|p.Gly220Glu S103
29365 BAA01g20700 A01 10224606 C T missense_variant MODERATE c.871C>T|p.Leu291Phe S303
29366 BAA01g20700 A01 10224770 G A synonymous_variant LOW c.939G>A|p.Arg313Arg S308
29367 BAA01g20700 A01 10224861 C T missense_variant MODERATE c.1030C>T|p.Pro344Ser S164
29368 BAA01g20700 A01 10224995 G A synonymous_variant LOW c.1164G>A|p.Pro388Pro S180
29369 BAA01g20690 A01 10225886 G A upstream_gene_variant MODIFIER c.-3579C>T| S246
29370 BAA01g20690 A01 10226164 C T upstream_gene_variant MODIFIER c.-3857G>A| S104
S184
29371 BAA01g20690 A01 10226758 G A upstream_gene_variant MODIFIER c.-4451C>T| S209
29372 BAA01g20690 A01 10226884 C T upstream_gene_variant MODIFIER c.-4577G>A| S158
29373 BAA01g20710 A01 10227062 G A splice_region_variant&synonymous_variant LOW c.294C>T|p.Gly98Gly S165
29374 BAA01g20710 A01 10227258 G A synonymous_variant LOW c.174C>T|p.Leu58Leu S236
29375 BAA01g20700 A01 10227325 C T downstream_gene_variant MODIFIER c.*2291C>T| S164