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
94751 BAA10g03660 A10 1770924 G A upstream_gene_variant MODIFIER c.-1998C>T| S217
94752 BAA10g03670 A10 1771381 C T synonymous_variant LOW c.501G>A|p.Gly167Gly S252
94753 BAA10g03670 A10 1771538 G A missense_variant MODERATE c.344C>T|p.Pro115Leu S283
94754 BAA10g03670 A10 1771633 G A synonymous_variant LOW c.249C>T|p.His83His S274
94755 BAA10g03670 A10 1771652 G A missense_variant MODERATE c.230C>T|p.Pro77Leu S43
94756 BAA10g03660 A10 1772015 G A upstream_gene_variant MODIFIER c.-3089C>T| S295
94757 BAA10g03660 A10 1772299 G A upstream_gene_variant MODIFIER c.-3373C>T| S65
94758 BAA10g03680 A10 1773112 G A missense_variant MODERATE c.640G>A|p.Val214Ile S164
94759 BAA10g03660 A10 1773729 G A upstream_gene_variant MODIFIER c.-4803C>T| S234
94760 BAA10g03690 A10 1773761 T G stop_lost&splice_region_variant HIGH c.1623A>C|p.Ter541Tyrext*? S199
94761 BAA10g03690 A10 1773762 T G stop_lost&splice_region_variant HIGH c.1622A>C|p.Ter541Serext*? S199
94762 BAA10g03670 A10 1774506 C T upstream_gene_variant MODIFIER c.-2625G>A| S42
94763 BAA10g03670 A10 1774913 C T upstream_gene_variant MODIFIER c.-3032G>A| S19
94764 BAA10g03690 A10 1775750 G A missense_variant MODERATE c.736C>T|p.Pro246Ser S134
94765 BAA10g03670 A10 1776072 G A upstream_gene_variant MODIFIER c.-4191C>T| S158
94766 BAA10g03690 A10 1776599 G A missense_variant MODERATE c.346C>T|p.Leu116Phe S59
94767 BAA10g03690 A10 1777282 C T missense_variant MODERATE c.70G>A|p.Glu24Lys S247
94768 BAA10g03690 A10 1777315 C T missense_variant MODERATE c.37G>A|p.Ala13Thr S2
94769 BAA10g03690 A10 1777721 G A upstream_gene_variant MODIFIER c.-370C>T| S60
94770 BAA10g03690 A10 1777884 G A upstream_gene_variant MODIFIER c.-533C>T| S81
94771 BAA10g03690 A10 1779534 G A upstream_gene_variant MODIFIER c.-2183C>T| S17
S176
94772 BAA10g03690 A10 1780212 G A upstream_gene_variant MODIFIER c.-2861C>T| S83
S88
94773 BAA10g03700 A10 1783509 G A missense_variant MODERATE c.742C>T|p.Pro248Ser S18
94774 BAA10g03720 A10 1784075 G A upstream_gene_variant MODIFIER c.-3703G>A| S148
S210
S30
94775 BAA10g03700 A10 1785081 C T missense_variant MODERATE c.64G>A|p.Gly22Ser S19