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
115551 BAA10g09880 A10 11720743 C T missense_variant MODERATE c.263G>A|p.Gly88Asp S117
115552 BAA10g09880 A10 11721158 G A upstream_gene_variant MODIFIER c.-153C>T| S172
S217
115553 BAA10g09880 A10 11721680 G A upstream_gene_variant MODIFIER c.-675C>T| S226
115554 BAA10g09880 A10 11721911 C T upstream_gene_variant MODIFIER c.-906G>A| S191
115555 BAA10g09880 A10 11722975 C T upstream_gene_variant MODIFIER c.-1970G>A| S61
115556 BAA10g09880 A10 11723208 G A upstream_gene_variant MODIFIER c.-2203C>T| S306
115557 BAA10g09880 A10 11723587 C T upstream_gene_variant MODIFIER c.-2582G>A| S199
115558 BAA10g09880 A10 11723609 C T upstream_gene_variant MODIFIER c.-2604G>A| S89
115559 BAA10g09880 A10 11723722 C T upstream_gene_variant MODIFIER c.-2717G>A| S200
115560 BAA10g09880 A10 11723804 G A upstream_gene_variant MODIFIER c.-2799C>T| S80
115561 BAA10g09880 A10 11724623 C T upstream_gene_variant MODIFIER c.-3618G>A| S264
115562 BAA10g09880 A10 11725932 G A upstream_gene_variant MODIFIER c.-4927C>T| S168
115563 BAA10g09890 A10 11726486 G A missense_variant MODERATE c.4G>A|p.Val2Met S290
115564 BAA10g09890 A10 11726528 C T missense_variant MODERATE c.46C>T|p.Pro16Ser S162
115565 BAA10g09890 A10 11726570 C T missense_variant MODERATE c.88C>T|p.Arg30Cys S247
115566 BAA10g09890 A10 11726684 G A missense_variant MODERATE c.202G>A|p.Gly68Arg S262
115567 BAA10g09890 A10 11727137 C T intron_variant MODIFIER c.242-76C>T| S246
115568 BAA10g09890 A10 11727252 C T missense_variant MODERATE c.281C>T|p.Pro94Leu S208
S93
115569 BAA10g09890 A10 11727295 C T synonymous_variant LOW c.324C>T|p.His108His S269
115570 BAA10g09890 A10 11727362 G A missense_variant MODERATE c.391G>A|p.Asp131Asn S65
115571 BAA10g09890 A10 11727453 G A intron_variant MODIFIER c.433-45G>A| S75
S81
115572 BAA10g09890 A10 11728160 G A downstream_gene_variant MODIFIER c.*354G>A| S302
115573 BAA10g09890 A10 11728513 C T downstream_gene_variant MODIFIER c.*707C>T| S70
115574 BAA10g09890 A10 11728843 C T downstream_gene_variant MODIFIER c.*1037C>T| S146
115575 BAA10g09890 A10 11729395 C T downstream_gene_variant MODIFIER c.*1589C>T| S149