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
131901 BAA10g19000 A10 17599909 G A missense_variant MODERATE c.1444G>A|p.Ala482Thr S74
131902 BAA10g19000 A10 17600384 G A downstream_gene_variant MODIFIER c.*440G>A| S126
131903 BAA10g19000 A10 17600896 C T downstream_gene_variant MODIFIER c.*952C>T| S20
131904 BAA10g19010 A10 17601282 C T missense_variant MODERATE c.1342G>A|p.Glu448Lys S168
131905 BAA10g19010 A10 17602119 G A synonymous_variant LOW c.768C>T|p.Asn256Asn S208
S219
131906 BAA10g19010 A10 17602344 C T synonymous_variant LOW c.630G>A|p.Gln210Gln S199
131907 BAA10g19010 A10 17602368 C T synonymous_variant LOW c.606G>A|p.Leu202Leu S298
131908 BAA10g19030 A10 17602437 C T upstream_gene_variant MODIFIER c.-4937C>T| S51
131909 BAA10g19010 A10 17603654 C T upstream_gene_variant MODIFIER c.-437G>A| S51
131910 BAA10g19010 A10 17603786 C T upstream_gene_variant MODIFIER c.-569G>A| S281
131911 BAA10g19010 A10 17604057 C T upstream_gene_variant MODIFIER c.-840G>A| S60
131912 BAA10g19020 A10 17604334 G T missense_variant MODERATE c.200C>A|p.Ser67Tyr S134
131913 BAA10g19020 A10 17604342 C T synonymous_variant LOW c.192G>A|p.Glu64Glu S243
131914 BAA10g19020 A10 17604580 G A missense_variant MODERATE c.31C>T|p.His11Tyr S223
131915 BAA10g19010 A10 17604662 G A upstream_gene_variant MODIFIER c.-1445C>T| S126
131916 BAA10g19010 A10 17604783 G A upstream_gene_variant MODIFIER c.-1566C>T| S63
131917 BAA10g19010 A10 17605536 G A upstream_gene_variant MODIFIER c.-2319C>T| S163
131918 BAA10g19010 A10 17605610 G A upstream_gene_variant MODIFIER c.-2393C>T| S158
131919 BAA10g19010 A10 17606900 G A upstream_gene_variant MODIFIER c.-3683C>T| S100
131920 BAA10g19030 A10 17608621 G A missense_variant MODERATE c.541G>A|p.Ala181Thr S193
131921 BAA10g19020 A10 17608942 G A upstream_gene_variant MODIFIER c.-4332C>T| S148
S210
131922 BAA10g19020 A10 17609015 C T upstream_gene_variant MODIFIER c.-4405G>A| S113
131923 BAA10g19030 A10 17610193 G A downstream_gene_variant MODIFIER c.*832G>A| S192
131924 BAA10g19040 A10 17612311 C T upstream_gene_variant MODIFIER c.-1157G>A| S54
131925 BAA10g19040 A10 17613923 G A upstream_gene_variant MODIFIER c.-2769C>T| S217