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
152401 BAA02g01020 A02 469112 G A upstream_gene_variant MODIFIER c.-7G>A| S303
152402 BAA02g01020 A02 469198 C T missense_variant MODERATE c.80C>T|p.Pro27Leu S225
152403 BAA02g01010 A02 471100 G A downstream_gene_variant MODIFIER c.*4288G>A| S168
152404 BAA02g01030 A02 473045 C T missense_variant MODERATE c.508G>A|p.Glu170Lys S38
152405 BAA02g01030 A02 475051 G A upstream_gene_variant MODIFIER c.-949C>T| S155
S211
152406 BAA02g01030 A02 475809 G A upstream_gene_variant MODIFIER c.-1707C>T| S161
152407 BAA02g01030 A02 476355 G A upstream_gene_variant MODIFIER c.-2253C>T| S127
152408 BAA02g01030 A02 476963 G A upstream_gene_variant MODIFIER c.-2861C>T| S64
152409 BAA02g01040 A02 479131 G A upstream_gene_variant MODIFIER c.-214C>T| S163
152410 BAA02g01040 A02 479545 G A upstream_gene_variant MODIFIER c.-628C>T| S50
152411 BAA02g01040 A02 479558 C T upstream_gene_variant MODIFIER c.-641G>A| S234
152412 BAA02g01040 A02 480749 G A upstream_gene_variant MODIFIER c.-1832C>T| S122
152413 BAA02g01050 A02 480970 C T synonymous_variant LOW c.37C>T|p.Leu13Leu S278
152414 BAA02g01050 A02 481274 C T synonymous_variant LOW c.234C>T|p.Gly78Gly S216
152415 BAA02g01040 A02 481519 G A upstream_gene_variant MODIFIER c.-2602C>T| S289
S290
152416 BAA02g01050 A02 483085 G A missense_variant MODERATE c.883G>A|p.Gly295Ser S69
152417 BAA02g01050 A02 483244 C T missense_variant MODERATE c.1042C>T|p.Leu348Phe S240
152418 BAA02g01070 A02 485189 C T upstream_gene_variant MODIFIER c.-3354C>T| S281
152419 BAA02g01070 A02 485332 C T upstream_gene_variant MODIFIER c.-3211C>T| S15
S3
152420 BAA02g01070 A02 486343 C T upstream_gene_variant MODIFIER c.-2200C>T| S267
152421 BAA02g01070 A02 486631 G A upstream_gene_variant MODIFIER c.-1912G>A| S90
152422 BAA02g01060 A02 487201 G A missense_variant MODERATE c.496G>A|p.Gly166Ser S187
152423 BAA02g01060 A02 487600 C T missense_variant MODERATE c.631C>T|p.Pro211Ser S306
S308
152424 BAA02g01060 A02 487646 C T missense_variant MODERATE c.677C>T|p.Ser226Phe S301
S304
152425 BAA02g01070 A02 489155 G A missense_variant MODERATE c.355G>A|p.Asp119Asn S12