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
151901 BAA02g00490 A02 275111 G A missense_variant MODERATE c.1478G>A|p.Gly493Glu S78
S83
151902 BAA02g00490 A02 275803 C T missense_variant MODERATE c.2170C>T|p.Pro724Ser S218
151903 BAA02g00490 A02 276554 G A synonymous_variant LOW c.2493G>A|p.Gln831Gln S265
151904 BAA02g00490 A02 276742 G A missense_variant MODERATE c.2681G>A|p.Gly894Asp S259
151905 BAA02g00490 A02 277100 C T missense_variant MODERATE c.2957C>T|p.Ala986Val S207
151906 BAA02g00490 A02 277370 G A missense_variant MODERATE c.3227G>A|p.Gly1076Glu S107
151907 BAA02g00490 A02 277436 C T missense_variant MODERATE c.3293C>T|p.Pro1098Leu S142
151908 BAA02g00490 A02 277850 C T missense_variant MODERATE c.3515C>T|p.Ala1172Val S171
151909 BAA02g00490 A02 279153 C T synonymous_variant LOW c.4500C>T|p.Leu1500Leu S272
151910 BAA02g00490 A02 279973 G A missense_variant MODERATE c.5077G>A|p.Asp1693Asn S241
151911 BAA02g00490 A02 280614 C T missense_variant MODERATE c.5620C>T|p.Leu1874Phe S121
151912 BAA02g00490 A02 280661 G A splice_donor_variant&intron_variant HIGH c.5666+1G>A| S173
151913 BAA02g00500 A02 283468 C T upstream_gene_variant MODIFIER c.-1081G>A| S45
151914 BAA02g00500 A02 283484 G A upstream_gene_variant MODIFIER c.-1097C>T| S38
151915 BAA02g00520 A02 289248 G A upstream_gene_variant MODIFIER c.-878G>A| S246
151916 BAA02g00530 A02 290502 C T upstream_gene_variant MODIFIER c.-2468C>T| S211
S227
151917 BAA02g00530 A02 290973 C T upstream_gene_variant MODIFIER c.-1997C>T| S115
151918 BAA02g00520 A02 291238 G A synonymous_variant LOW c.198G>A|p.Arg66Arg S45
151919 BAA02g00530 A02 292300 C T upstream_gene_variant MODIFIER c.-670C>T| S185
151920 BAA02g00530 A02 292466 G A upstream_gene_variant MODIFIER c.-504G>A| S244
151921 BAA02g00530 A02 292908 G A upstream_gene_variant MODIFIER c.-62G>A| S173
151922 BAA02g00530 A02 293294 G A splice_region_variant&intron_variant LOW c.160-6G>A| S59
151923 BAA02g00510 A02 293474 G A downstream_gene_variant MODIFIER c.*4595G>A| S286
151924 BAA02g00520 A02 296011 G A downstream_gene_variant MODIFIER c.*4470G>A| S161
151925 BAA02g00530 A02 296900 G A downstream_gene_variant MODIFIER c.*2989G>A| S174