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
133051 BAA10g19670 A10 17979804 G A missense_variant MODERATE c.1178C>T|p.Thr393Met S38
133052 BAA10g19670 A10 17979965 G A synonymous_variant LOW c.1017C>T|p.Tyr339Tyr S67
133053 BAA10g19670 A10 17980104 C T missense_variant MODERATE c.878G>A|p.Arg293Lys S92
133054 BAA10g19670 A10 17980117 G A missense_variant MODERATE c.865C>T|p.Pro289Ser S71
133055 BAA10g19670 A10 17980140 G A missense_variant MODERATE c.842C>T|p.Ser281Phe S94
133056 BAA10g19670 A10 17980954 C T missense_variant MODERATE c.545G>A|p.Gly182Glu S297
133057 BAA10g19670 A10 17982224 C T upstream_gene_variant MODIFIER c.-555G>A| S242
133058 BAA10g19670 A10 17985121 G A upstream_gene_variant MODIFIER c.-3452C>T| S286
133059 BAA10g19670 A10 17985907 G A upstream_gene_variant MODIFIER c.-4238C>T| S181
133060 BAA10g19690 A10 17987190 G A downstream_gene_variant MODIFIER c.*2934C>T| S208
S219
133061 BAA10g19690 A10 17987364 G A downstream_gene_variant MODIFIER c.*2760C>T| S212
133062 BAA10g19690 A10 17987662 G A downstream_gene_variant MODIFIER c.*2462C>T| S165
133063 BAA10g19690 A10 17988717 C T downstream_gene_variant MODIFIER c.*1407G>A| S281
133064 BAA10g19690 A10 17990155 C T missense_variant MODERATE c.2120G>A|p.Ser707Asn S119
133065 BAA10g19680 A10 17990655 C T upstream_gene_variant MODIFIER c.-1618G>A| S87
133066 BAA10g19690 A10 17990774 C T missense_variant MODERATE c.1756G>A|p.Val586Met S51
133067 BAA10g19690 A10 17990857 C T missense_variant MODERATE c.1673G>A|p.Gly558Glu S170
133068 BAA10g19680 A10 17990951 C T upstream_gene_variant MODIFIER c.-1914G>A| S146
133069 BAA10g19690 A10 17991640 G A missense_variant MODERATE c.1580C>T|p.Ser527Leu S184
133070 BAA10g19690 A10 17991778 C T missense_variant MODERATE c.1442G>A|p.Arg481His S259
133071 BAA10g19690 A10 17991800 C T missense_variant MODERATE c.1420G>A|p.Asp474Asn S46
133072 BAA10g19690 A10 17992172 C T missense_variant MODERATE c.1048G>A|p.Asp350Asn S116
133073 BAA10g19690 A10 17992228 G A missense_variant MODERATE c.992C>T|p.Ser331Phe S39
133074 BAA10g19690 A10 17992388 C T missense_variant MODERATE c.832G>A|p.Glu278Lys S283
133075 BAA10g19680 A10 17992920 C T upstream_gene_variant MODIFIER c.-3883G>A| S68