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
160351 BAA02g07580 A02 3257627 G A upstream_gene_variant MODIFIER c.-4634G>A| S236
160352 BAA02g07580 A02 3259399 G A upstream_gene_variant MODIFIER c.-2862G>A| S85
160353 BAA02g07570 A02 3260228 C T synonymous_variant LOW c.561G>A|p.Glu187Glu S283
160354 BAA02g07570 A02 3263096 C T upstream_gene_variant MODIFIER c.-1925G>A| S99
160355 BAA02g07570 A02 3264390 C T upstream_gene_variant MODIFIER c.-3219G>A| S262
160356 BAA02g07590 A02 3265661 C T missense_variant MODERATE c.211G>A|p.Ala71Thr S117
160357 BAA02g07600 A02 3266765 G A missense_variant MODERATE c.153G>A|p.Met51Ile S148
S210
S30
S31
160358 BAA02g07590 A02 3266918 C T upstream_gene_variant MODIFIER c.-1047G>A| S73
S91
160359 BAA02g07590 A02 3268034 G A upstream_gene_variant MODIFIER c.-2163C>T| S287
160360 BAA02g07600 A02 3268216 C T missense_variant MODERATE c.737C>T|p.Ser246Phe S251
160361 BAA02g07590 A02 3268378 C T upstream_gene_variant MODIFIER c.-2507G>A| S167
160362 BAA02g07600 A02 3268455 G A missense_variant MODERATE c.895G>A|p.Gly299Arg S266
160363 BAA02g07600 A02 3268741 C T stop_gained HIGH c.1024C>T|p.Gln342* S263
160364 BAA02g07590 A02 3268821 C T upstream_gene_variant MODIFIER c.-2950G>A| S120
160365 BAA02g07590 A02 3269277 G A upstream_gene_variant MODIFIER c.-3406C>T| S265
160366 BAA02g07600 A02 3270164 C T missense_variant MODERATE c.1817C>T|p.Ser606Phe S97
160367 BAA02g07590 A02 3270496 G A upstream_gene_variant MODIFIER c.-4625C>T| S74
160368 BAA02g07590 A02 3270546 G A upstream_gene_variant MODIFIER c.-4675C>T| S197
160369 BAA02g07590 A02 3270751 C T upstream_gene_variant MODIFIER c.-4880G>A| S129
160370 BAA02g07590 A02 3270763 G A upstream_gene_variant MODIFIER c.-4892C>T| S23
160371 BAA02g07610 A02 3271919 G A upstream_gene_variant MODIFIER c.-772G>A| S163
160372 BAA02g07610 A02 3271997 C T upstream_gene_variant MODIFIER c.-694C>T| S211
S227
160373 BAA02g07610 A02 3272627 C T upstream_gene_variant MODIFIER c.-64C>T| S51
160374 BAA02g07610 A02 3273547 A T missense_variant MODERATE c.857A>T|p.Lys286Met S242
160375 BAA02g07600 A02 3273804 C T downstream_gene_variant MODIFIER c.*3612C>T| S196