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
158451 BAA02g06050 A02 2577193 C T upstream_gene_variant MODIFIER c.-2023G>A| S68
158452 BAA02g06050 A02 2578126 C T upstream_gene_variant MODIFIER c.-2956G>A| S272
158453 BAA02g06050 A02 2578893 G A upstream_gene_variant MODIFIER c.-3723C>T| S305
158454 BAA02g06060 A02 2580069 T G synonymous_variant LOW c.267T>G|p.Leu89Leu S186
158455 BAA02g06060 A02 2580363 G C synonymous_variant LOW c.561G>C|p.Gly187Gly S91
158456 BAA02g06060 A02 2580372 T C synonymous_variant LOW c.570T>C|p.Tyr190Tyr S91
158457 BAA02g06060 A02 2580378 G T synonymous_variant LOW c.576G>T|p.Ala192Ala S91
158458 BAA02g06060 A02 2580387 G T synonymous_variant LOW c.585G>T|p.Leu195Leu S91
158459 BAA02g06060 A02 2580514 G A missense_variant MODERATE c.712G>A|p.Glu238Lys S109
158460 BAA02g06060 A02 2580537 G A synonymous_variant LOW c.735G>A|p.Glu245Glu S187
158461 BAA02g06070 A02 2582028 C T upstream_gene_variant MODIFIER c.-2259C>T| S295
158462 BAA02g06070 A02 2583101 G A upstream_gene_variant MODIFIER c.-1186G>A| S132
S137
S215
158463 BAA02g06070 A02 2583729 C T upstream_gene_variant MODIFIER c.-558C>T| S216
158464 BAA02g06070 A02 2583927 G A upstream_gene_variant MODIFIER c.-360G>A| S256
158465 BAA02g06070 A02 2584357 G A missense_variant MODERATE c.71G>A|p.Ser24Asn S192
158466 BAA02g06070 A02 2584394 G A synonymous_variant LOW c.108G>A|p.Lys36Lys S231
158467 BAA02g06070 A02 2584657 C T missense_variant&splice_region_variant MODERATE c.263C>T|p.Thr88Met S33
158468 BAA02g06070 A02 2584845 G A synonymous_variant LOW c.372G>A|p.Glu124Glu S247
158469 BAA02g06070 A02 2586543 C T downstream_gene_variant MODIFIER c.*854C>T| S42
158470 BAA02g06080 A02 2587726 G A synonymous_variant LOW c.478C>T|p.Leu160Leu S174
158471 BAA02g06080 A02 2587991 G A missense_variant MODERATE c.409C>T|p.Leu137Phe S110
158472 BAA02g06080 A02 2588178 C T synonymous_variant LOW c.336G>A|p.Thr112Thr S46
158473 BAA02g06080 A02 2590189 G A upstream_gene_variant MODIFIER c.-1261C>T| S5
158474 BAA02g06090 A02 2592039 G A missense_variant MODERATE c.14G>A|p.Arg5His S79
S91
158475 BAA02g06090 A02 2592048 C T missense_variant MODERATE c.23C>T|p.Pro8Leu S111