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
201001 BAA02g30650 A02 17981041 C T upstream_gene_variant MODIFIER c.-2908C>T| S308
201002 BAA02g30650 A02 17981113 C T upstream_gene_variant MODIFIER c.-2836C>T| S124
201003 BAA02g30650 A02 17981152 C T upstream_gene_variant MODIFIER c.-2797C>T| S239
201004 BAA02g30650 A02 17983957 C T synonymous_variant LOW c.9C>T|p.Asn3Asn S2
201005 BAA02g30650 A02 17984094 C T missense_variant MODERATE c.146C>T|p.Ser49Leu S276
201006 BAA02g30650 A02 17984302 C T synonymous_variant LOW c.354C>T|p.Asp118Asp S91
201007 BAA02g30650 A02 17984305 T C synonymous_variant LOW c.357T>C|p.Ile119Ile S91
201008 BAA02g30660 A02 17984876 C T downstream_gene_variant MODIFIER c.*2652G>A| S51
201009 BAA02g30650 A02 17985276 C T synonymous_variant LOW c.621C>T|p.Thr207Thr S147
S91
201010 BAA02g30650 A02 17985285 T C synonymous_variant LOW c.630T>C|p.Phe210Phe S147
S91
201011 BAA02g30650 A02 17985293 G C missense_variant MODERATE c.638G>C|p.Ser213Thr S147
S91
201012 BAA02g30650 A02 17985294 T C synonymous_variant LOW c.639T>C|p.Ser213Ser S147
S91
201013 BAA02g30650 A02 17985757 C T downstream_gene_variant MODIFIER c.*367C>T| S239
201014 BAA02g30650 A02 17986023 T A downstream_gene_variant MODIFIER c.*633T>A| S189
201015 BAA02g30670 A02 17989019 G A upstream_gene_variant MODIFIER c.-4961G>A| S256
201016 BAA02g30670 A02 17989146 G A upstream_gene_variant MODIFIER c.-4834G>A| S287
201017 BAA02g30660 A02 17992406 G A upstream_gene_variant MODIFIER c.-2753C>T| S74
201018 BAA02g30660 A02 17992870 G A upstream_gene_variant MODIFIER c.-3217C>T| S200
201019 BAA02g30670 A02 17999228 C T synonymous_variant LOW c.3936C>T|p.Phe1312Phe S275
201020 BAA02g30670 A02 17999530 C T missense_variant MODERATE c.4159C>T|p.Leu1387Phe S46
201021 BAA02g30670 A02 17999702 G A missense_variant MODERATE c.4331G>A|p.Cys1444Tyr S279
201022 BAA02g30670 A02 17999890 C T missense_variant MODERATE c.4396C>T|p.Leu1466Phe S75
S81
201023 BAA02g30670 A02 18001471 C T downstream_gene_variant MODIFIER c.*815C>T| S2
201024 BAA02g30670 A02 18003472 G A downstream_gene_variant MODIFIER c.*2816G>A| S26
201025 BAA02g30670 A02 18003939 G A downstream_gene_variant MODIFIER c.*3283G>A| S156
S263