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
93551 BAA10g02890 A10 1408310 C T downstream_gene_variant MODIFIER c.*495G>A| S40
S49
93552 BAA10g02890 A10 1408712 C T downstream_gene_variant MODIFIER c.*93G>A| S205
93553 BAA10g02890 A10 1409107 C T missense_variant MODERATE c.335G>A|p.Gly112Glu S23
93554 BAA10g02890 A10 1409354 C T splice_donor_variant&intron_variant HIGH c.173+1G>A| S180
93555 BAA10g02890 A10 1409590 G A upstream_gene_variant MODIFIER c.-63C>T| S57
93556 BAA10g02890 A10 1409909 C T upstream_gene_variant MODIFIER c.-382G>A| S44
93557 BAA10g02890 A10 1410733 G A upstream_gene_variant MODIFIER c.-1206C>T| S295
93558 BAA10g02890 A10 1410861 G A upstream_gene_variant MODIFIER c.-1334C>T| S67
93559 BAA10g02890 A10 1411166 C T upstream_gene_variant MODIFIER c.-1639G>A| S88
93560 BAA10g02890 A10 1411484 G A upstream_gene_variant MODIFIER c.-1957C>T| S107
93561 BAA10g02890 A10 1413180 C T upstream_gene_variant MODIFIER c.-3653G>A| S260
93562 BAA10g02890 A10 1413791 G A upstream_gene_variant MODIFIER c.-4264C>T| S100
93563 BAA10g02900 A10 1414981 C T upstream_gene_variant MODIFIER c.-2223C>T| S152
93564 BAA10g02900 A10 1415747 C T upstream_gene_variant MODIFIER c.-1457C>T| S143
93565 BAA10g02900 A10 1416171 G A upstream_gene_variant MODIFIER c.-1033G>A| S302
93566 BAA10g02900 A10 1416393 G A upstream_gene_variant MODIFIER c.-811G>A| S85
93567 BAA10g02900 A10 1416661 G A upstream_gene_variant MODIFIER c.-543G>A| S107
93568 BAA10g02900 A10 1417914 C T missense_variant MODERATE c.394C>T|p.Leu132Phe S60
93569 BAA10g02900 A10 1419004 G A downstream_gene_variant MODIFIER c.*411G>A| S32
93570 BAA10g02900 A10 1419887 G A downstream_gene_variant MODIFIER c.*1294G>A| S48
93571 BAA10g02900 A10 1420338 G A downstream_gene_variant MODIFIER c.*1745G>A| S158
93572 BAA10g02900 A10 1420876 G A downstream_gene_variant MODIFIER c.*2283G>A| S255
93573 BAA10g02910 A10 1421190 C T missense_variant MODERATE c.305G>A|p.Gly102Glu S202
93574 BAA10g02910 A10 1421246 C T synonymous_variant LOW c.249G>A|p.Val83Val S11
93575 BAA10g02910 A10 1421747 G A splice_region_variant&intron_variant LOW c.152+6C>T| S133