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
130551 BAA10g18090 A10 17107531 G A upstream_gene_variant MODIFIER c.-1436G>A| S161
130552 BAA10g18090 A10 17107967 C T upstream_gene_variant MODIFIER c.-1000C>T| S257
130553 BAA10g18090 A10 17108077 T C upstream_gene_variant MODIFIER c.-890T>C| S208
S219
130554 BAA10g18090 A10 17109486 G A missense_variant MODERATE c.520G>A|p.Gly174Arg S1
S90
130555 BAA10g18090 A10 17109690 G A missense_variant MODERATE c.724G>A|p.Ala242Thr S198
130556 BAA10g18090 A10 17109835 G A missense_variant MODERATE c.869G>A|p.Gly290Glu S89
130557 BAA10g18100 A10 17110194 G A upstream_gene_variant MODIFIER c.-192G>A| S61
130558 BAA10g18100 A10 17110218 C T upstream_gene_variant MODIFIER c.-168C>T| S281
130559 BAA10g18110 A10 17111318 C G upstream_gene_variant MODIFIER c.-670C>G| S59
130560 BAA10g18110 A10 17112136 G A missense_variant MODERATE c.149G>A|p.Gly50Glu S63
130561 BAA10g18110 A10 17112807 C T missense_variant MODERATE c.820C>T|p.Pro274Ser S23
130562 BAA10g18090 A10 17113435 C T downstream_gene_variant MODIFIER c.*3416C>T| S286
130563 BAA10g18090 A10 17113671 C T downstream_gene_variant MODIFIER c.*3652C>T| S45
130564 BAA10g18120 A10 17113874 G A upstream_gene_variant MODIFIER c.-4897G>A| S16
130565 BAA10g18120 A10 17116730 C T upstream_gene_variant MODIFIER c.-2041C>T| S256
130566 BAA10g18120 A10 17117204 G A upstream_gene_variant MODIFIER c.-1567G>A| S198
130567 BAA10g18120 A10 17117711 C T upstream_gene_variant MODIFIER c.-1060C>T| S204
130568 BAA10g18120 A10 17117763 C T upstream_gene_variant MODIFIER c.-1008C>T| S260
130569 BAA10g18120 A10 17118088 C T upstream_gene_variant MODIFIER c.-683C>T| S286
130570 BAA10g18120 A10 17118417 G A upstream_gene_variant MODIFIER c.-354G>A| S175
130571 BAA10g18120 A10 17118555 C T upstream_gene_variant MODIFIER c.-216C>T| S113
130572 BAA10g18120 A10 17119391 C T synonymous_variant LOW c.621C>T|p.Thr207Thr S306
130573 BAA10g18120 A10 17119471 C T missense_variant MODERATE c.701C>T|p.Pro234Leu S188
130574 BAA10g18120 A10 17119555 C T missense_variant MODERATE c.785C>T|p.Ser262Phe S26
130575 BAA10g18140 A10 17120501 G A upstream_gene_variant MODIFIER c.-4041G>A| S262