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
128601 BAA10g16730-BAA10g16740 A10 16395666 G A intergenic_region MODIFIER n.16395666G>A| S178
128602 BAA10g16730-BAA10g16740 A10 16395884 G A intergenic_region MODIFIER n.16395884G>A| S67
128603 BAA10g16730-BAA10g16740 A10 16396234 C T intergenic_region MODIFIER n.16396234C>T| S2
128604 BAA10g16730-BAA10g16740 A10 16396743 C T intergenic_region MODIFIER n.16396743C>T| S231
128605 BAA10g16740 A10 16397912 C T upstream_gene_variant MODIFIER c.-4612C>T| S235
128606 BAA10g16740 A10 16398155 G A upstream_gene_variant MODIFIER c.-4369G>A| S290
128607 BAA10g16740 A10 16398631 C T upstream_gene_variant MODIFIER c.-3893C>T| S175
128608 BAA10g16740 A10 16398889 C T upstream_gene_variant MODIFIER c.-3635C>T| S189
128609 BAA10g16740 A10 16399767 G A upstream_gene_variant MODIFIER c.-2757G>A| S128
128610 BAA10g16740 A10 16402461 C T upstream_gene_variant MODIFIER c.-63C>T| S48
128611 BAA10g16750 A10 16402804 G A downstream_gene_variant MODIFIER c.*2534C>T| S270
128612 BAA10g16750 A10 16403590 C T downstream_gene_variant MODIFIER c.*1748G>A| S123
128613 BAA10g16740 A10 16403760 C T synonymous_variant LOW c.321C>T|p.Asn107Asn S277
128614 BAA10g16740 A10 16403989 G A missense_variant MODERATE c.550G>A|p.Asp184Asn S160
128615 BAA10g16740 A10 16404275 G A missense_variant MODERATE c.836G>A|p.Arg279Gln S174
S216
S241
S265
128616 BAA10g16740 A10 16404397 G A missense_variant MODERATE c.958G>A|p.Ala320Thr S138
128617 BAA10g16740 A10 16404516 G A synonymous_variant LOW c.1077G>A|p.Ala359Ala S198
128618 BAA10g16740 A10 16404652 G A missense_variant MODERATE c.1213G>A|p.Asp405Asn S148
S30
S31
128619 BAA10g16740 A10 16404676 G A missense_variant MODERATE c.1237G>A|p.Glu413Lys S129
128620 BAA10g16740 A10 16404717 C T synonymous_variant LOW c.1278C>T|p.Phe426Phe S119
128621 BAA10g16740 A10 16404858 G A synonymous_variant LOW c.1419G>A|p.Ala473Ala S125
128622 BAA10g16740 A10 16406165 C T downstream_gene_variant MODIFIER c.*1073C>T| S259
128623 BAA10g16750 A10 16406525 C T missense_variant MODERATE c.545G>A|p.Gly182Asp S168
128624 BAA10g16750 A10 16406918 G A missense_variant MODERATE c.308C>T|p.Thr103Ile S40
S49
128625 BAA10g16750 A10 16407060 C A missense_variant MODERATE c.231G>T|p.Trp77Cys S6