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
149751 BAA10g33830 A10 23976784 T C upstream_gene_variant MODIFIER c.-2918A>G| S218
149752 BAA10g33840 A10 23977359 C T missense_variant MODERATE c.203C>T|p.Ala68Val S262
149753 BAA10g33840 A10 23977460 C T missense_variant MODERATE c.304C>T|p.Arg102Cys S150
149754 BAA10g33850 A10 23977959 G A stop_gained HIGH c.922C>T|p.Gln308* S200
149755 BAA10g33830 A10 23978021 G A upstream_gene_variant MODIFIER c.-4155C>T| S261
149756 BAA10g33850 A10 23978220 G A synonymous_variant LOW c.783C>T|p.Thr261Thr S57
149757 BAA10g33840 A10 23979701 G A downstream_gene_variant MODIFIER c.*2221G>A| S43
149758 BAA10g33850 A10 23980434 G A upstream_gene_variant MODIFIER c.-286C>T| S202
149759 BAA10g33850 A10 23981588 G A upstream_gene_variant MODIFIER c.-1440C>T| S303
149760 BAA10g33860 A10 23981894 C T missense_variant MODERATE c.496G>A|p.Glu166Lys S80
149761 BAA10g33860 A10 23982299 C T missense_variant MODERATE c.154G>A|p.Gly52Ser S281
149762 BAA10g33870 A10 23984236 C T missense_variant MODERATE c.3106G>A|p.Ala1036Thr S221
149763 BAA10g33870 A10 23984769 G A missense_variant MODERATE c.2573C>T|p.Ser858Phe S70
149764 BAA10g33870 A10 23984780 C T synonymous_variant LOW c.2562G>A|p.Glu854Glu S25
149765 BAA10g33870 A10 23985638 C T synonymous_variant LOW c.1704G>A|p.Lys568Lys S292
149766 BAA10g33870 A10 23986914 C T missense_variant MODERATE c.580G>A|p.Gly194Arg S44
149767 BAA10g33870 A10 23989084 C T upstream_gene_variant MODIFIER c.-1295G>A| S221
149768 BAA10g33870 A10 23989130 C T upstream_gene_variant MODIFIER c.-1341G>A| S186
S296
149769 BAA10g33870 A10 23992144 C T upstream_gene_variant MODIFIER c.-4355G>A| S148
S30
S31
149770 BAA10g33880 A10 23993282 G A upstream_gene_variant MODIFIER c.-4G>A| S250
149771 BAA10g33880 A10 23995032 C T missense_variant MODERATE c.1373C>T|p.Thr458Ile S11
149772 BAA10g33890 A10 23995360 A T downstream_gene_variant MODIFIER c.*615T>A| S303
149773 BAA10g33890 A10 23996044 C T synonymous_variant LOW c.1650G>A|p.Thr550Thr S48
149774 BAA10g33890 A10 23996211 G A synonymous_variant LOW c.1483C>T|p.Leu495Leu S185
149775 BAA10g33880 A10 23996968 G A downstream_gene_variant MODIFIER c.*1311G>A| S202