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
121051 BAA10g12190 A10 13647501 C T missense_variant MODERATE c.487G>A|p.Asp163Asn S256
121052 BAA10g12190 A10 13647660 G A missense_variant MODERATE c.328C>T|p.Leu110Phe S303
121053 BAA10g12190 A10 13647940 G A synonymous_variant LOW c.48C>T|p.Ala16Ala S171
121054 BAA10g12190 A10 13648333 G A upstream_gene_variant MODIFIER c.-346C>T| S159
S243
121055 BAA10g12190 A10 13648646 G A upstream_gene_variant MODIFIER c.-659C>T| S150
121056 BAA10g12190 A10 13649289 G A upstream_gene_variant MODIFIER c.-1302C>T| S75
S81
121057 BAA10g12190 A10 13650595 G A upstream_gene_variant MODIFIER c.-2608C>T| S198
121058 BAA10g12190 A10 13650610 G A upstream_gene_variant MODIFIER c.-2623C>T| S75
121059 BAA10g12190 A10 13652638 C T upstream_gene_variant MODIFIER c.-4651G>A| S302
S89
121060 BAA10g12200 A10 13653081 C T upstream_gene_variant MODIFIER c.-1435C>T| S10
121061 BAA10g12200 A10 13653249 C T upstream_gene_variant MODIFIER c.-1267C>T| S282
121062 BAA10g12200 A10 13654218 G A upstream_gene_variant MODIFIER c.-298G>A| S273
121063 BAA10g12200 A10 13654552 C T intron_variant MODIFIER c.8+29C>T| S53
121064 BAA10g12200 A10 13655628 C T intron_variant MODIFIER c.514-41C>T| S167
121065 BAA10g12200 A10 13656047 G A missense_variant MODERATE c.739G>A|p.Val247Met S241
121066 BAA10g12210 A10 13656522 G A upstream_gene_variant MODIFIER c.-4875G>A| S100
121067 BAA10g12210 A10 13656847 C T upstream_gene_variant MODIFIER c.-4550C>T| S249
121068 BAA10g12210 A10 13657465 G A upstream_gene_variant MODIFIER c.-3932G>A| S129
121069 BAA10g12210 A10 13657501 C T upstream_gene_variant MODIFIER c.-3896C>T| S224
121070 BAA10g12210 A10 13657858 G A upstream_gene_variant MODIFIER c.-3539G>A| S158
121071 BAA10g12200 A10 13658155 G A synonymous_variant LOW c.1635G>A|p.Gln545Gln S228
121072 BAA10g12200 A10 13658598 G A missense_variant MODERATE c.1921G>A|p.Glu641Lys S97
121073 BAA10g12210 A10 13659255 G A upstream_gene_variant MODIFIER c.-2142G>A| S176
121074 BAA10g12210 A10 13659487 G A upstream_gene_variant MODIFIER c.-1910G>A| S289
121075 BAA10g12210 A10 13660106 C T upstream_gene_variant MODIFIER c.-1291C>T| S92