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
14351 BAA01g11180 A01 5166433 C T missense_variant MODERATE c.946G>A|p.Val316Ile S230
14352 BAA01g11180 A01 5166520 C T missense_variant MODERATE c.859G>A|p.Glu287Lys S170
14353 BAA01g11180 A01 5166673 C T missense_variant MODERATE c.706G>A|p.Glu236Lys S182
14354 BAA01g11180 A01 5167987 C T upstream_gene_variant MODIFIER c.-609G>A| S255
14355 BAA01g11180 A01 5168059 C T upstream_gene_variant MODIFIER c.-681G>A| S18
14356 BAA01g11180 A01 5168646 G A upstream_gene_variant MODIFIER c.-1268C>T| S209
14357 BAA01g11180 A01 5168929 G A upstream_gene_variant MODIFIER c.-1551C>T| S274
14358 BAA01g11180 A01 5169158 C T upstream_gene_variant MODIFIER c.-1780G>A| S242
14359 BAA01g11180 A01 5170359 C T upstream_gene_variant MODIFIER c.-2981G>A| S125
14360 BAA01g11180 A01 5171516 G A upstream_gene_variant MODIFIER c.-4138C>T| S274
14361 BAA01g11180 A01 5171914 C T upstream_gene_variant MODIFIER c.-4536G>A| S249
14362 BAA01g11200 A01 5172904 C T missense_variant MODERATE c.1393G>A|p.Asp465Asn S176
14363 BAA01g11200 A01 5173141 C T missense_variant MODERATE c.1156G>A|p.Glu386Lys S1
S90
14364 BAA01g11200 A01 5173508 C T synonymous_variant LOW c.789G>A|p.Glu263Glu S185
14365 BAA01g11200 A01 5173571 C T synonymous_variant LOW c.726G>A|p.Gly242Gly S135
14366 BAA01g11200 A01 5173901 C T synonymous_variant LOW c.396G>A|p.Gln132Gln S164
14367 BAA01g11200 A01 5175860 G A upstream_gene_variant MODIFIER c.-1564C>T| S63
14368 BAA01g11200 A01 5176328 G A upstream_gene_variant MODIFIER c.-2032C>T| S245
14369 BAA01g11200 A01 5177025 G A upstream_gene_variant MODIFIER c.-2729C>T| S122
14370 BAA01g11200 A01 5177707 C T upstream_gene_variant MODIFIER c.-3411G>A| S69
14371 BAA01g11200 A01 5178236 G A upstream_gene_variant MODIFIER c.-3940C>T| S116
S148
S295
S296
S30
S31
S54
14372 BAA01g11210 A01 5180660 C T synonymous_variant LOW c.178C>T|p.Leu60Leu S158
14373 BAA01g11210 A01 5181051 G A synonymous_variant LOW c.501G>A|p.Lys167Lys S14
14374 BAA01g11210 A01 5181407 C T missense_variant MODERATE c.695C>T|p.Ala232Val S213
14375 BAA01g11210 A01 5181824 G A missense_variant&splice_region_variant MODERATE c.943G>A|p.Ala315Thr S280