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
84151 BAA01g44610 A01 29701491 C T missense_variant MODERATE c.532G>A|p.Glu178Lys S45
84152 BAA01g44610 A01 29701525 C T synonymous_variant LOW c.498G>A|p.Ser166Ser S132
S215
84153 BAA01g44610 A01 29701620 G A missense_variant MODERATE c.403C>T|p.Pro135Ser S5
84154 BAA01g44610 A01 29701786 G A synonymous_variant LOW c.237C>T|p.Phe79Phe S189
84155 BAA01g44610 A01 29701989 G A missense_variant MODERATE c.34C>T|p.Pro12Ser S265
84156 BAA01g44610 A01 29702003 G A missense_variant MODERATE c.20C>T|p.Ser7Leu S241
84157 BAA01g44610 A01 29702354 G A upstream_gene_variant MODIFIER c.-332C>T| S42
84158 BAA01g44630 A01 29704414 G A synonymous_variant LOW c.234G>A|p.Gln78Gln S278
84159 BAA01g44630 A01 29705168 C T missense_variant MODERATE c.910C>T|p.Pro304Ser S162
84160 BAA01g44610 A01 29705428 C T upstream_gene_variant MODIFIER c.-3406G>A| S32
84161 BAA01g44610 A01 29706159 C T upstream_gene_variant MODIFIER c.-4137G>A| S242
84162 BAA01g44640 A01 29707820 C T missense_variant MODERATE c.1036G>A|p.Gly346Ser S274
84163 BAA01g44640 A01 29707942 C T missense_variant MODERATE c.914G>A|p.Ser305Asn S182
84164 BAA01g44630 A01 29708374 G A downstream_gene_variant MODIFIER c.*2484G>A| S238
84165 BAA01g44640 A01 29708944 C T missense_variant MODERATE c.302G>A|p.Gly101Asp S164
84166 BAA01g44630 A01 29709695 C T downstream_gene_variant MODIFIER c.*3805C>T| S191
84167 BAA01g44640 A01 29712145 G A upstream_gene_variant MODIFIER c.-2060C>T| S202
84168 BAA01g44640 A01 29712525 T A upstream_gene_variant MODIFIER c.-2440A>T| S35
84169 BAA01g44640 A01 29713105 C T upstream_gene_variant MODIFIER c.-3020G>A| S11
84170 BAA01g44640 A01 29713322 C T upstream_gene_variant MODIFIER c.-3237G>A| S165
84171 BAA01g44640 A01 29714107 C T upstream_gene_variant MODIFIER c.-4022G>A| S25
84172 BAA01g44640 A01 29714118 C T upstream_gene_variant MODIFIER c.-4033G>A| S57
84173 BAA01g44640 A01 29714318 G A upstream_gene_variant MODIFIER c.-4233C>T| S175
84174 BAA01g44640 A01 29714379 G A upstream_gene_variant MODIFIER c.-4294C>T| S199
84175 BAA01g44640 A01 29714383 T A upstream_gene_variant MODIFIER c.-4298A>T| S134