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
124951 BAA10g14310 A10 15080066 G A missense_variant MODERATE c.59C>T|p.Thr20Ile S85
124952 BAA10g14310 A10 15080245 G A upstream_gene_variant MODIFIER c.-121C>T| S198
124953 BAA10g14310 A10 15080778 G A upstream_gene_variant MODIFIER c.-654C>T| S125
124954 BAA10g14310 A10 15080793 A T upstream_gene_variant MODIFIER c.-669T>A| S293
124955 BAA10g14310 A10 15081135 G A upstream_gene_variant MODIFIER c.-1011C>T| S62
124956 BAA10g14320 A10 15081987 C T synonymous_variant LOW c.177C>T|p.Ser59Ser S26
124957 BAA10g14320 A10 15082783 G A missense_variant MODERATE c.973G>A|p.Glu325Lys S241
124958 BAA10g14320 A10 15083399 C T missense_variant MODERATE c.1406C>T|p.Ser469Phe S195
124959 BAA10g14310 A10 15083958 C T upstream_gene_variant MODIFIER c.-3834G>A| S259
124960 BAA10g14310 A10 15084892 T A upstream_gene_variant MODIFIER c.-4768A>T| S276
124961 BAA10g14310 A10 15085007 C T upstream_gene_variant MODIFIER c.-4883G>A| S298
124962 BAA10g14330 A10 15085682 G A upstream_gene_variant MODIFIER c.-969C>T| S198
124963 BAA10g14330 A10 15085726 G A upstream_gene_variant MODIFIER c.-1013C>T| S217
S248
124964 BAA10g14330 A10 15086179 C T upstream_gene_variant MODIFIER c.-1466G>A| S183
124965 BAA10g14330 A10 15086186 C A upstream_gene_variant MODIFIER c.-1473G>T| S76
124966 BAA10g14330 A10 15086243 G A upstream_gene_variant MODIFIER c.-1530C>T| S18
124967 BAA10g14340 A10 15086390 C T missense_variant MODERATE c.94C>T|p.Pro32Ser S193
S255
124968 BAA10g14340 A10 15086511 C T missense_variant MODERATE c.215C>T|p.Ala72Val S143
124969 BAA10g14340 A10 15087549 C T missense_variant MODERATE c.1253C>T|p.Ser418Phe S140
124970 BAA10g14340 A10 15087758 C T missense_variant MODERATE c.1462C>T|p.His488Tyr S133
124971 BAA10g14340 A10 15088075 C T synonymous_variant LOW c.1779C>T|p.Arg593Arg S247
124972 BAA10g14340 A10 15088344 C T missense_variant MODERATE c.2048C>T|p.Pro683Leu S86
124973 BAA10g14340 A10 15092873 G A downstream_gene_variant MODIFIER c.*532G>A| S57
124974 BAA10g14350 A10 15093886 C T missense_variant MODERATE c.1696G>A|p.Ala566Thr S176
124975 BAA10g14350 A10 15094761 G A missense_variant MODERATE c.892C>T|p.Pro298Ser S198