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
20551 BAA01g15160 A01 7259004 C T upstream_gene_variant MODIFIER c.-1003G>A| S8
20552 BAA01g15160 A01 7259043 G A upstream_gene_variant MODIFIER c.-1042C>T| S34
20553 BAA01g15160 A01 7259067 C T upstream_gene_variant MODIFIER c.-1066G>A| S48
20554 BAA01g15160 A01 7260242 C T upstream_gene_variant MODIFIER c.-2241G>A| S134
20555 BAA01g15160 A01 7260367 C T upstream_gene_variant MODIFIER c.-2366G>A| S198
20556 BAA01g15170 A01 7261016 G A missense_variant MODERATE c.1160C>T|p.Thr387Ile S95
20557 BAA01g15160 A01 7261643 C T upstream_gene_variant MODIFIER c.-3642G>A| S128
20558 BAA01g15160 A01 7261878 G A upstream_gene_variant MODIFIER c.-3877C>T| S178
20559 BAA01g15160 A01 7262374 G A upstream_gene_variant MODIFIER c.-4373C>T| S272
20560 BAA01g15170 A01 7262795 G A missense_variant MODERATE c.602C>T|p.Thr201Ile S239
20561 BAA01g15170 A01 7262905 A G synonymous_variant LOW c.492T>C|p.Asp164Asp S232
20562 BAA01g15170 A01 7263368 C T stop_gained HIGH c.29G>A|p.Trp10* S179
20563 BAA01g15170 A01 7264662 G A upstream_gene_variant MODIFIER c.-1266C>T| S72
S78
20564 BAA01g15170 A01 7265517 G A upstream_gene_variant MODIFIER c.-2121C>T| S163
20565 BAA01g15170 A01 7265871 G A upstream_gene_variant MODIFIER c.-2475C>T| S262
20566 BAA01g15170 A01 7266217 G A upstream_gene_variant MODIFIER c.-2821C>T| S276
20567 BAA01g15170 A01 7267265 G A upstream_gene_variant MODIFIER c.-3869C>T| S306
20568 BAA01g15170 A01 7268016 G A upstream_gene_variant MODIFIER c.-4620C>T| S202
20569 BAA01g15170 A01 7268218 C T upstream_gene_variant MODIFIER c.-4822G>A| S159
S243
20570 BAA01g15170 A01 7268237 G A upstream_gene_variant MODIFIER c.-4841C>T| S92
20571 BAA01g15180 A01 7268442 G A upstream_gene_variant MODIFIER c.-605G>A| S163
20572 BAA01g15180 A01 7269043 G A upstream_gene_variant MODIFIER c.-4G>A| S180
20573 BAA01g15180 A01 7269229 C T synonymous_variant LOW c.183C>T|p.Phe61Phe S247
20574 BAA01g15180 A01 7269687 G A intron_variant MODIFIER c.338+47G>A| S217
20575 BAA01g15180 A01 7269753 G A intron_variant MODIFIER c.339-9G>A| S175