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
751 BAA01g00520 A01 257797 C T synonymous_variant LOW c.7689C>T|p.Leu2563Leu S265
752 BAA01g00520 A01 258248 C T missense_variant MODERATE c.7969C>T|p.Leu2657Phe S267
753 BAA01g00520 A01 258803 C T synonymous_variant LOW c.8301C>T|p.His2767His S206
S26
754 BAA01g00520 A01 259051 C T synonymous_variant LOW c.8430C>T|p.Phe2810Phe S182
755 BAA01g00520 A01 259752 G A synonymous_variant LOW c.8958G>A|p.Glu2986Glu S136
756 BAA01g00520 A01 260886 G A downstream_gene_variant MODIFIER c.*690G>A| S177
757 BAA01g00520 A01 261231 C T downstream_gene_variant MODIFIER c.*1035C>T| S212
758 BAA01g00520 A01 261456 G A downstream_gene_variant MODIFIER c.*1260G>A| S247
759 BAA01g00520 A01 261918 C T downstream_gene_variant MODIFIER c.*1722C>T| S53
760 BAA01g00520 A01 262656 G A downstream_gene_variant MODIFIER c.*2460G>A| S197
761 BAA01g00540 A01 262887 C T upstream_gene_variant MODIFIER c.-4972C>T| S273
762 BAA01g00540 A01 262921 G A upstream_gene_variant MODIFIER c.-4938G>A| S294
763 BAA01g00540 A01 263688 C T upstream_gene_variant MODIFIER c.-4171C>T| S20
764 BAA01g00530 A01 264494 G A synonymous_variant LOW c.891C>T|p.Thr297Thr S218
765 BAA01g00530 A01 265488 C T splice_region_variant&synonymous_variant LOW c.345G>A|p.Gln115Gln S176
766 BAA01g00540 A01 265677 G A upstream_gene_variant MODIFIER c.-2182G>A| S260
767 BAA01g00540 A01 265685 C T upstream_gene_variant MODIFIER c.-2174C>T| S246
768 BAA01g00540 A01 265754 G A upstream_gene_variant MODIFIER c.-2105G>A| S28
769 BAA01g00530 A01 267298 G A upstream_gene_variant MODIFIER c.-693C>T| S259
770 BAA01g00540 A01 268052 C T missense_variant MODERATE c.194C>T|p.Ser65Phe S244
771 BAA01g00540 A01 269391 G A missense_variant MODERATE c.823G>A|p.Asp275Asn S301
S304
772 BAA01g00530 A01 270202 C T upstream_gene_variant MODIFIER c.-3597G>A| S273
773 BAA01g00550 A01 270524 G A synonymous_variant LOW c.288C>T|p.Leu96Leu S260
774 BAA01g00550 A01 270613 C T missense_variant MODERATE c.199G>A|p.Glu67Lys S255
775 BAA01g00550 A01 270672 G A missense_variant MODERATE c.140C>T|p.Pro47Leu S7