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
140701 BAA10g25800 A10 20699022 G A missense_variant MODERATE c.1555C>T|p.Leu519Phe S81
S85
140702 BAA10g25800 A10 20699230 G A synonymous_variant LOW c.1347C>T|p.Ile449Ile S9
140703 BAA10g25800 A10 20699247 G A synonymous_variant LOW c.1330C>T|p.Leu444Leu S158
140704 BAA10g25800 A10 20699671 G A synonymous_variant LOW c.906C>T|p.Leu302Leu S160
140705 BAA10g25800 A10 20700002 C T missense_variant MODERATE c.575G>A|p.Arg192His S18
140706 BAA10g25800 A10 20701449 C T upstream_gene_variant MODIFIER c.-873G>A| S16
140707 BAA10g25800 A10 20701622 C T upstream_gene_variant MODIFIER c.-1046G>A| S14
140708 BAA10g25800 A10 20701813 C T upstream_gene_variant MODIFIER c.-1237G>A| S157
140709 BAA10g25800 A10 20701902 C A upstream_gene_variant MODIFIER c.-1326G>T| S5
140710 BAA10g25800 A10 20701903 G A upstream_gene_variant MODIFIER c.-1327C>T| S159
S243
140711 BAA10g25800 A10 20702027 G A upstream_gene_variant MODIFIER c.-1451C>T| S261
140712 BAA10g25800 A10 20702036 G A upstream_gene_variant MODIFIER c.-1460C>T| S262
140713 BAA10g25800 A10 20702211 G A upstream_gene_variant MODIFIER c.-1635C>T| S273
140714 BAA10g25800 A10 20703443 C T upstream_gene_variant MODIFIER c.-2867G>A| S23
140715 BAA10g25800 A10 20704816 C T upstream_gene_variant MODIFIER c.-4240G>A| S260
140716 BAA10g25810 A10 20706399 C T upstream_gene_variant MODIFIER c.-1953G>A| S251
140717 BAA10g25820 A10 20707273 C T missense_variant MODERATE c.799C>T|p.Leu267Phe S40
S49
140718 BAA10g25820 A10 20707315 G A missense_variant MODERATE c.841G>A|p.Glu281Lys S262
140719 BAA10g25820 A10 20709161 G A missense_variant MODERATE c.1609G>A|p.Asp537Asn S112
140720 BAA10g25830 A10 20711045 G A synonymous_variant LOW c.714G>A|p.Lys238Lys S114
S256
140721 BAA10g25830 A10 20712569 G A synonymous_variant LOW c.1209G>A|p.Lys403Lys S103
140722 BAA10g25830 A10 20712921 G A missense_variant MODERATE c.1379G>A|p.Arg460Lys S263
140723 BAA10g25830 A10 20713689 G A missense_variant MODERATE c.1747G>A|p.Asp583Asn S62
140724 BAA10g25830 A10 20713925 G A synonymous_variant LOW c.1983G>A|p.Arg661Arg S16
140725 BAA10g25840 A10 20715156 G A splice_acceptor_variant&intron_variant HIGH c.190-1G>A| S230