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
131851 BAA10g18980 A10 17584368 C T downstream_gene_variant MODIFIER c.*1884C>T| S305
131852 BAA10g18990 A10 17584660 G A missense_variant MODERATE c.1108C>T|p.Pro370Ser S167
131853 BAA10g18990 A10 17584702 G A missense_variant MODERATE c.1066C>T|p.Arg356Cys S233
131854 BAA10g18990 A10 17584763 G A synonymous_variant LOW c.1005C>T|p.Tyr335Tyr S63
131855 BAA10g18980 A10 17585072 T A downstream_gene_variant MODIFIER c.*2588T>A| S26
131856 BAA10g18990 A10 17586053 C T missense_variant MODERATE c.229G>A|p.Glu77Lys S60
131857 BAA10g18990 A10 17586069 C T synonymous_variant LOW c.213G>A|p.Arg71Arg S269
131858 BAA10g18990 A10 17588115 G A upstream_gene_variant MODIFIER c.-714C>T| S295
131859 BAA10g18990 A10 17588634 C T upstream_gene_variant MODIFIER c.-1233G>A| S202
131860 BAA10g18990 A10 17589597 C T upstream_gene_variant MODIFIER c.-2196G>A| S119
131861 BAA10g18990 A10 17589681 C T upstream_gene_variant MODIFIER c.-2280G>A| S108
131862 BAA10g18990 A10 17589748 C T upstream_gene_variant MODIFIER c.-2347G>A| S160
131863 BAA10g18990 A10 17590334 C T upstream_gene_variant MODIFIER c.-2933G>A| S2
131864 BAA10g18990 A10 17590653 G A upstream_gene_variant MODIFIER c.-3252C>T| S180
131865 BAA10g18990 A10 17590865 A C upstream_gene_variant MODIFIER c.-3464T>G| S54
131866 BAA10g18990 A10 17592117 C T upstream_gene_variant MODIFIER c.-4716G>A| S146
131867 BAA10g18990 A10 17592277 C T upstream_gene_variant MODIFIER c.-4876G>A| S10
131868 BAA10g19000 A10 17595019 G A upstream_gene_variant MODIFIER c.-1211G>A| S184
131869 BAA10g19000 A10 17595027 G A upstream_gene_variant MODIFIER c.-1203G>A| S36
131870 BAA10g19000 A10 17595897 C T upstream_gene_variant MODIFIER c.-333C>T| S123
131871 BAA10g19010 A10 17596634 G A downstream_gene_variant MODIFIER c.*4371C>T| S166
131872 BAA10g19000 A10 17598022 C T synonymous_variant LOW c.573C>T|p.Phe191Phe S70
131873 BAA10g19000 A10 17598340 C T missense_variant MODERATE c.821C>T|p.Ala274Val S23
131874 BAA10g19000 A10 17598348 G A missense_variant&splice_region_variant MODERATE c.829G>A|p.Glu277Lys S251
131875 BAA10g19010 A10 17599747 C T downstream_gene_variant MODIFIER c.*1258G>A| S107