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
70451 BAA01g36890 A01 24667704 G A upstream_gene_variant MODIFIER c.-2273C>T| S5
70452 BAA01g36890 A01 24668067 G A upstream_gene_variant MODIFIER c.-2636C>T| S271
70453 BAA01g36890 A01 24668575 G A upstream_gene_variant MODIFIER c.-3144C>T| S191
70454 BAA01g36890 A01 24668802 C T upstream_gene_variant MODIFIER c.-3371G>A| S153
70455 BAA01g36890 A01 24668875 G A upstream_gene_variant MODIFIER c.-3444C>T| S152
70456 BAA01g36890 A01 24669477 C T upstream_gene_variant MODIFIER c.-4046G>A| S217
S248
70457 BAA01g36890 A01 24669595 C T upstream_gene_variant MODIFIER c.-4164G>A| S286
70458 BAA01g36890 A01 24670281 C T upstream_gene_variant MODIFIER c.-4850G>A| S11
70459 BAA01g36900 A01 24670668 C T downstream_gene_variant MODIFIER c.*1252G>A| S201
70460 BAA01g36900 A01 24672236 C T missense_variant MODERATE c.1033G>A|p.Val345Met S18
70461 BAA01g36910 A01 24672575 C T downstream_gene_variant MODIFIER c.*2288G>A| S104
S52
70462 BAA01g36900 A01 24673296 C T splice_acceptor_variant&intron_variant HIGH c.289-1G>A| S284
70463 BAA01g36900 A01 24673629 G A missense_variant MODERATE c.118C>T|p.Leu40Phe S181
70464 BAA01g36900 A01 24673914 C T upstream_gene_variant MODIFIER c.-168G>A| S293
70465 BAA01g36910 A01 24675062 C T missense_variant MODERATE c.803G>A|p.Gly268Asp S142
70466 BAA01g36910 A01 24675063 C T missense_variant MODERATE c.802G>A|p.Gly268Ser S32
70467 BAA01g36910 A01 24675180 C T missense_variant MODERATE c.685G>A|p.Val229Ile S4
70468 BAA01g36910 A01 24675682 C T missense_variant MODERATE c.260G>A|p.Gly87Glu S12
70469 BAA01g36910 A01 24675743 C T missense_variant MODERATE c.199G>A|p.Val67Ile S81
S85
70470 BAA01g36900 A01 24677104 G A upstream_gene_variant MODIFIER c.-3358C>T| S212
70471 BAA01g36900 A01 24677646 G A upstream_gene_variant MODIFIER c.-3900C>T| S175
70472 BAA01g36920 A01 24678190 C T splice_acceptor_variant&intron_variant HIGH c.173-1G>A| S17
70473 BAA01g36900 A01 24678267 C T upstream_gene_variant MODIFIER c.-4521G>A| S230
70474 BAA01g36910 A01 24679515 C T upstream_gene_variant MODIFIER c.-3413G>A| S50
70475 BAA01g36910 A01 24679942 C T upstream_gene_variant MODIFIER c.-3840G>A| S11
S53