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
66001 BAA01g34560 A01 23109160 G A downstream_gene_variant MODIFIER c.*3547C>T| S169
66002 BAA01g34560 A01 23109757 C T downstream_gene_variant MODIFIER c.*2950G>A| S92
66003 BAA01g34560 A01 23110344 C T downstream_gene_variant MODIFIER c.*2363G>A| S303
66004 BAA01g34560 A01 23110600 G A downstream_gene_variant MODIFIER c.*2107C>T| S80
66005 BAA01g34560 A01 23110728 C T downstream_gene_variant MODIFIER c.*1979G>A| S219
S39
S72
66006 BAA01g34560 A01 23111796 G A downstream_gene_variant MODIFIER c.*911C>T| S38
66007 BAA01g34560 A01 23111845 C T downstream_gene_variant MODIFIER c.*862G>A| S128
66008 BAA01g34560 A01 23118448 C T missense_variant MODERATE c.1777G>A|p.Val593Ile S48
66009 BAA01g34560 A01 23119244 G A synonymous_variant LOW c.981C>T|p.Val327Val S155
66010 BAA01g34560 A01 23119290 G A missense_variant MODERATE c.935C>T|p.Ala312Val S25
66011 BAA01g34560 A01 23119437 C T missense_variant MODERATE c.874G>A|p.Asp292Asn S182
66012 BAA01g34560 A01 23119553 G A missense_variant MODERATE c.758C>T|p.Pro253Leu S221
66013 BAA01g34560 A01 23119646 C T missense_variant MODERATE c.665G>A|p.Gly222Glu S264
66014 BAA01g34560 A01 23119719 G A missense_variant MODERATE c.592C>T|p.Leu198Phe S96
66015 BAA01g34560 A01 23120018 C T missense_variant MODERATE c.293G>A|p.Arg98Lys S295
66016 BAA01g34560 A01 23120090 G A missense_variant MODERATE c.221C>T|p.Thr74Met S308
66017 BAA01g34560 A01 23120172 C T missense_variant MODERATE c.139G>A|p.Ala47Thr S51
66018 BAA01g34560 A01 23120284 G A synonymous_variant LOW c.27C>T|p.Ile9Ile S201
66019 BAA01g34560 A01 23120415 C T upstream_gene_variant MODIFIER c.-105G>A| S231
66020 BAA01g34560 A01 23121215 G A upstream_gene_variant MODIFIER c.-905C>T| S245
66021 BAA01g34560 A01 23121309 C T upstream_gene_variant MODIFIER c.-999G>A| S282
66022 BAA01g34560 A01 23121410 C T upstream_gene_variant MODIFIER c.-1100G>A| S219
S72
66023 BAA01g34560 A01 23121458 C T upstream_gene_variant MODIFIER c.-1148G>A| S208
S93
66024 BAA01g34560 A01 23121513 G A upstream_gene_variant MODIFIER c.-1203C>T| S160
66025 BAA01g34560 A01 23121851 C T upstream_gene_variant MODIFIER c.-1541G>A| S11