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
115751 BAA10g09940-BAA10g09950 A10 11769223 C T intergenic_region MODIFIER n.11769223C>T| S301
S304
115752 BAA10g09940-BAA10g09950 A10 11769519 G A intergenic_region MODIFIER n.11769519G>A| S111
115753 BAA10g09940-BAA10g09950 A10 11770047 C T intergenic_region MODIFIER n.11770047C>T| S166
115754 BAA10g09940-BAA10g09950 A10 11771993 C T intergenic_region MODIFIER n.11771993C>T| S270
115755 BAA10g09940-BAA10g09950 A10 11773199 T A intergenic_region MODIFIER n.11773199T>A| S77
S82
115756 BAA10g09940-BAA10g09950 A10 11774785 G A intergenic_region MODIFIER n.11774785G>A| S283
115757 BAA10g09950 A10 11775534 C T upstream_gene_variant MODIFIER c.-4720C>T| S157
S163
S20
S43
115758 BAA10g09950 A10 11777585 G A upstream_gene_variant MODIFIER c.-2669G>A| S4
115759 BAA10g09950 A10 11779612 C T upstream_gene_variant MODIFIER c.-642C>T| S92
115760 BAA10g09960 A10 11782323 G A missense_variant MODERATE c.452G>A|p.Arg151Lys S18
115761 BAA10g09950 A10 11784150 G A downstream_gene_variant MODIFIER c.*3582G>A| S62
115762 BAA10g09960 A10 11788281 G A downstream_gene_variant MODIFIER c.*3558G>A| S81
115763 BAA10g09960 A10 11788660 G A downstream_gene_variant MODIFIER c.*3937G>A| S57
115764 BAA10g09980 A10 11790084 G A synonymous_variant LOW c.63C>T|p.Leu21Leu S62
115765 BAA10g09970 A10 11790638 G A upstream_gene_variant MODIFIER c.-1589C>T| S240
115766 BAA10g09970 A10 11793438 C T upstream_gene_variant MODIFIER c.-4389G>A| S42
115767 BAA10g09990 A10 11794753 C T missense_variant MODERATE c.89C>T|p.Ser30Phe S273
115768 BAA10g09990 A10 11794769 C T synonymous_variant LOW c.105C>T|p.Asn35Asn S294
115769 BAA10g09990 A10 11795519 G A downstream_gene_variant MODIFIER c.*144G>A| S262
115770 BAA10g09990 A10 11797006 C T downstream_gene_variant MODIFIER c.*1631C>T| S174
115771 BAA10g09990 A10 11797012 C A downstream_gene_variant MODIFIER c.*1637C>A| S23
S294
115772 BAA10g09990 A10 11797572 G A downstream_gene_variant MODIFIER c.*2197G>A| S192
115773 BAA10g09990 A10 11798403 C T downstream_gene_variant MODIFIER c.*3028C>T| S10
115774 BAA10g09990 A10 11798479 C T downstream_gene_variant MODIFIER c.*3104C>T| S241
115775 BAA10g10000 A10 11799145 G A upstream_gene_variant MODIFIER c.-4391G>A| S259