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
131401 BAA10g18640 A10 17398357 C T upstream_gene_variant MODIFIER c.-1024G>A| S197
131402 BAA10g18650 A10 17399302 G A synonymous_variant LOW c.774G>A|p.Arg258Arg S169
131403 BAA10g18650 A10 17399671 C T synonymous_variant LOW c.1074C>T|p.Ile358Ile S173
131404 BAA10g18650 A10 17400639 C T stop_gained HIGH c.1966C>T|p.Gln656* S56
131405 BAA10g18650 A10 17400738 C T missense_variant MODERATE c.2065C>T|p.Leu689Phe S274
131406 BAA10g18650 A10 17400829 G A missense_variant MODERATE c.2156G>A|p.Arg719Lys S176
131407 BAA10g18640 A10 17401276 C T upstream_gene_variant MODIFIER c.-3943G>A| S79
S91
131408 BAA10g18640 A10 17401721 G A upstream_gene_variant MODIFIER c.-4388C>T| S42
131409 BAA10g18640 A10 17401881 C T upstream_gene_variant MODIFIER c.-4548G>A| S70
131410 BAA10g18660 A10 17402975 C T upstream_gene_variant MODIFIER c.-1306G>A| S281
131411 BAA10g18660 A10 17403936 C T upstream_gene_variant MODIFIER c.-2267G>A| S206
131412 BAA10g18670 A10 17405196 G A missense_variant MODERATE c.911C>T|p.Ser304Leu S16
131413 BAA10g18670 A10 17405342 G A synonymous_variant LOW c.765C>T|p.His255His S262
131414 BAA10g18670 A10 17406700 G A upstream_gene_variant MODIFIER c.-64C>T| S134
131415 BAA10g18670 A10 17407187 C T upstream_gene_variant MODIFIER c.-551G>A| S238
131416 BAA10g18670 A10 17409073 C T upstream_gene_variant MODIFIER c.-2437G>A| S45
131417 BAA10g18670 A10 17410680 G A upstream_gene_variant MODIFIER c.-4044C>T| S38
131418 BAA10g18670 A10 17410781 G A upstream_gene_variant MODIFIER c.-4145C>T| S218
131419 BAA10g18680 A10 17413716 C T downstream_gene_variant MODIFIER c.*1185C>T| S54
131420 BAA10g18680 A10 17414715 C T downstream_gene_variant MODIFIER c.*2184C>T| S153
S213
131421 BAA10g18680 A10 17414815 G A downstream_gene_variant MODIFIER c.*2284G>A| S213
131422 BAA10g18680 A10 17416678 C T downstream_gene_variant MODIFIER c.*4147C>T| S177
131423 BAA10g18700 A10 17418973 G A upstream_gene_variant MODIFIER c.-4570G>A| S182
131424 BAA10g18700 A10 17419066 C T upstream_gene_variant MODIFIER c.-4477C>T| S170
131425 BAA10g18690 A10 17420929 C T missense_variant MODERATE c.1282G>A|p.Ala428Thr S45