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
118601 BAA10g11050 A10 12766045 C T missense_variant MODERATE c.244G>A|p.Glu82Lys S23
118602 BAA10g11040 A10 12766416 G A upstream_gene_variant MODIFIER c.-1098C>T| S157
S163
118603 BAA10g11040 A10 12766574 G A upstream_gene_variant MODIFIER c.-1256C>T| S18
118604 BAA10g11040 A10 12766631 G A upstream_gene_variant MODIFIER c.-1313C>T| S47
118605 BAA10g11040 A10 12766670 C T upstream_gene_variant MODIFIER c.-1352G>A| S135
118606 BAA10g11040 A10 12766727 G A upstream_gene_variant MODIFIER c.-1409C>T| S67
118607 BAA10g11040 A10 12766783 G A upstream_gene_variant MODIFIER c.-1465C>T| S263
118608 BAA10g11060 A10 12767150 C T missense_variant MODERATE c.137C>T|p.Ser46Phe S266
118609 BAA10g11060 A10 12767302 G A missense_variant MODERATE c.289G>A|p.Ala97Thr S219
S72
118610 BAA10g11060 A10 12767392 C T missense_variant MODERATE c.379C>T|p.Leu127Phe S244
118611 BAA10g11070 A10 12768976 G A missense_variant MODERATE c.380C>T|p.Ser127Phe S267
118612 BAA10g11040 A10 12770188 C T upstream_gene_variant MODIFIER c.-4870G>A| S76
118613 BAA10g11080 A10 12770280 G A missense_variant MODERATE c.70G>A|p.Ala24Thr S295
118614 BAA10g11080 A10 12770292 G A missense_variant MODERATE c.82G>A|p.Glu28Lys S262
118615 BAA10g11080 A10 12770304 G A missense_variant MODERATE c.94G>A|p.Glu32Lys S289
118616 BAA10g11080 A10 12770378 G A synonymous_variant LOW c.168G>A|p.Lys56Lys S216
118617 BAA10g11080 A10 12770957 C T synonymous_variant LOW c.747C>T|p.Ile249Ile S236
118618 BAA10g11090 A10 12771708 C T missense_variant MODERATE c.1249G>A|p.Asp417Asn S286
118619 BAA10g11090 A10 12772670 C T missense_variant MODERATE c.611G>A|p.Gly204Glu S143
118620 BAA10g11090 A10 12773093 G A missense_variant MODERATE c.368C>T|p.Ala123Val S234
118621 BAA10g11070 A10 12773624 A G upstream_gene_variant MODIFIER c.-3841T>C| S99
118622 BAA10g11100 A10 12776648 C T missense_variant MODERATE c.940C>T|p.Leu314Phe S113
118623 BAA10g11100 A10 12777041 G A missense_variant MODERATE c.1333G>A|p.Val445Met S1
S90
118624 BAA10g11100 A10 12777204 G A missense_variant MODERATE c.1496G>A|p.Gly499Glu S125
118625 BAA10g11100 A10 12777800 G A missense_variant MODERATE c.2014G>A|p.Val672Met S81
S85