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
94551 BAA10g03570 A10 1717897 G A missense_variant MODERATE c.842C>T|p.Pro281Leu S168
94552 BAA10g03570 A10 1717898 G A missense_variant MODERATE c.841C>T|p.Pro281Ser S129
94553 BAA10g03570 A10 1718651 G A missense_variant MODERATE c.88C>T|p.Leu30Phe S140
94554 BAA10g03570 A10 1719400 G A upstream_gene_variant MODIFIER c.-662C>T| S240
94555 BAA10g03570 A10 1720227 G A upstream_gene_variant MODIFIER c.-1489C>T| S133
94556 BAA10g03570 A10 1720474 G A upstream_gene_variant MODIFIER c.-1736C>T| S140
94557 BAA10g03570 A10 1720800 G A upstream_gene_variant MODIFIER c.-2062C>T| S283
94558 BAA10g03570 A10 1721281 G A upstream_gene_variant MODIFIER c.-2543C>T| S53
94559 BAA10g03570 A10 1721325 G A upstream_gene_variant MODIFIER c.-2587C>T| S184
94560 BAA10g03570 A10 1721964 C T upstream_gene_variant MODIFIER c.-3226G>A| S87
94561 BAA10g03570 A10 1723529 C T upstream_gene_variant MODIFIER c.-4791G>A| S74
94562 BAA10g03580 A10 1723860 G A downstream_gene_variant MODIFIER c.*2454C>T| S151
94563 BAA10g03580 A10 1724827 C T downstream_gene_variant MODIFIER c.*1487G>A| S67
94564 BAA10g03580 A10 1724993 T C downstream_gene_variant MODIFIER c.*1321A>G| S138
94565 BAA10g03580 A10 1726366 C T missense_variant MODERATE c.191G>A|p.Gly64Glu S263
94566 BAA10g03580 A10 1726867 C T upstream_gene_variant MODIFIER c.-231G>A| S113
94567 BAA10g03580 A10 1726924 G A upstream_gene_variant MODIFIER c.-288C>T| S171
94568 BAA10g03580 A10 1727077 G A upstream_gene_variant MODIFIER c.-441C>T| S86
94569 BAA10g03580 A10 1727352 A T upstream_gene_variant MODIFIER c.-716T>A| S304
94570 BAA10g03580 A10 1727722 C T upstream_gene_variant MODIFIER c.-1086G>A| S108
94571 BAA10g03580 A10 1727763 G A upstream_gene_variant MODIFIER c.-1127C>T| S192
94572 BAA10g03590 A10 1728210 G A missense_variant MODERATE c.1385C>T|p.Pro462Leu S43
94573 BAA10g03590 A10 1728664 G A missense_variant MODERATE c.931C>T|p.Leu311Phe S13
94574 BAA10g03590 A10 1729305 G A missense_variant MODERATE c.290C>T|p.Ala97Val S211
S227
94575 BAA10g03590 A10 1729363 C T missense_variant MODERATE c.232G>A|p.Asp78Asn S121