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
50451 BAA01g28380 A01 17414308 C T missense_variant MODERATE c.1384G>A|p.Asp462Asn S134
S263
50452 BAA01g28370 A01 17415185 C T downstream_gene_variant MODIFIER c.*3512C>T| S279
50453 BAA01g28380 A01 17415319 C T missense_variant MODERATE c.619G>A|p.Val207Ile S251
50454 BAA01g28370 A01 17415619 C T downstream_gene_variant MODIFIER c.*3946C>T| S112
50455 BAA01g28370 A01 17415801 C T downstream_gene_variant MODIFIER c.*4128C>T| S11
50456 BAA01g28370 A01 17416032 C T downstream_gene_variant MODIFIER c.*4359C>T| S132
S137
S215
50457 BAA01g28380 A01 17416181 G A synonymous_variant LOW c.387C>T|p.Asp129Asp S212
50458 BAA01g28380 A01 17416230 C T missense_variant MODERATE c.338G>A|p.Gly113Glu S99
50459 BAA01g28380 A01 17416512 C T missense_variant MODERATE c.56G>A|p.Gly19Glu S275
50460 BAA01g28380 A01 17416642 C T upstream_gene_variant MODIFIER c.-75G>A| S172
S217
50461 BAA01g28380 A01 17416792 G A upstream_gene_variant MODIFIER c.-225C>T| S117
50462 BAA01g28380 A01 17416877 C T upstream_gene_variant MODIFIER c.-310G>A| S54
50463 BAA01g28380 A01 17417340 C T upstream_gene_variant MODIFIER c.-773G>A| S171
50464 BAA01g28380 A01 17418839 G A upstream_gene_variant MODIFIER c.-2272C>T| S74
50465 BAA01g28380 A01 17420398 C T upstream_gene_variant MODIFIER c.-3831G>A| S39
50466 BAA01g28390 A01 17422188 G A upstream_gene_variant MODIFIER c.-1854G>A| S225
50467 BAA01g28390 A01 17423628 G A upstream_gene_variant MODIFIER c.-414G>A| S23
50468 BAA01g28390 A01 17423818 C T upstream_gene_variant MODIFIER c.-224C>T| S46
50469 BAA01g28390 A01 17423892 C T upstream_gene_variant MODIFIER c.-150C>T| S213
S42
50470 BAA01g28390 A01 17423982 C T upstream_gene_variant MODIFIER c.-60C>T| S67
50471 BAA01g28390 A01 17424326 C T missense_variant MODERATE c.188C>T|p.Ser63Phe S205
50472 BAA01g28390 A01 17424431 C T missense_variant MODERATE c.293C>T|p.Thr98Ile S14
S224
50473 BAA01g28390 A01 17424934 C T intron_variant MODIFIER c.435+261C>T| S153
50474 BAA01g28390 A01 17425452 C T intron_variant MODIFIER c.436-113C>T| S182
50475 BAA01g28390 A01 17426759 G A missense_variant MODERATE c.1630G>A|p.Ala544Thr S11