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
401 BAA01g00300 A01 150382 C T upstream_gene_variant MODIFIER c.-2234G>A| S4
402 BAA01g00300 A01 150469 G A upstream_gene_variant MODIFIER c.-2321C>T| S204
403 BAA01g00300 A01 150982 C T upstream_gene_variant MODIFIER c.-2834G>A| S97
404 BAA01g00300 A01 151262 C T upstream_gene_variant MODIFIER c.-3114G>A| S43
405 BAA01g00300 A01 151692 G A upstream_gene_variant MODIFIER c.-3544C>T| S168
406 BAA01g00320 A01 154278 G A downstream_gene_variant MODIFIER c.*3135C>T| S293
407 BAA01g00320 A01 154344 C T downstream_gene_variant MODIFIER c.*3069G>A| S46
408 BAA01g00310 A01 156850 G A downstream_gene_variant MODIFIER c.*357G>A| S262
409 BAA01g00310 A01 157130 C T downstream_gene_variant MODIFIER c.*637C>T| S203
410 BAA01g00310 A01 157232 A G downstream_gene_variant MODIFIER c.*739A>G| S67
411 BAA01g00310 A01 158028 G A downstream_gene_variant MODIFIER c.*1535G>A| S122
412 BAA01g00320 A01 158139 C T stop_gained HIGH c.2283G>A|p.Trp761* S135
413 BAA01g00320 A01 158249 C T missense_variant MODERATE c.2237G>A|p.Gly746Glu S1
S90
414 BAA01g00320 A01 158293 G A synonymous_variant LOW c.2193C>T|p.Leu731Leu S168
415 BAA01g00320 A01 158411 G A missense_variant MODERATE c.2075C>T|p.Ser692Phe S186
416 BAA01g00310 A01 159330 C T downstream_gene_variant MODIFIER c.*2837C>T| S249
417 BAA01g00310 A01 159485 C T downstream_gene_variant MODIFIER c.*2992C>T| S144
418 BAA01g00310 A01 159792 G A downstream_gene_variant MODIFIER c.*3299G>A| S232
419 BAA01g00320 A01 160161 C T missense_variant MODERATE c.1339G>A|p.Ala447Thr S74
420 BAA01g00310 A01 161004 C T downstream_gene_variant MODIFIER c.*4511C>T| S100
421 BAA01g00320 A01 161030 G A missense_variant MODERATE c.1277C>T|p.Ala426Val S200
422 BAA01g00320 A01 161163 C A missense_variant MODERATE c.1144G>T|p.Gly382Cys S237
423 BAA01g00320 A01 161563 G A intron_variant MODIFIER c.934+146C>T| S15
S3
424 BAA01g00320 A01 161629 G A intron_variant MODIFIER c.934+80C>T| S240
425 BAA01g00320 A01 161754 C T missense_variant MODERATE c.889G>A|p.Val297Ile S138