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
144951 BAA10g29610 A10 22214940 C T downstream_gene_variant MODIFIER c.*3296G>A| S247
144952 BAA10g29610 A10 22215021 T G downstream_gene_variant MODIFIER c.*3215A>C| S86
144953 BAA10g29610 A10 22215328 C T downstream_gene_variant MODIFIER c.*2908G>A| S155
S211
144954 BAA10g29610 A10 22215535 C T downstream_gene_variant MODIFIER c.*2701G>A| S230
144955 BAA10g29600 A10 22217832 G A downstream_gene_variant MODIFIER c.*1550G>A| S43
144956 BAA10g29610 A10 22218447 G A missense_variant MODERATE c.929C>T|p.Ala310Val S192
144957 BAA10g29610 A10 22218823 C T missense_variant MODERATE c.553G>A|p.Asp185Asn S9
144958 BAA10g29610 A10 22219239 G A missense_variant MODERATE c.137C>T|p.Thr46Ile S273
144959 BAA10g29610 A10 22219423 C T upstream_gene_variant MODIFIER c.-48G>A| S105
144960 BAA10g29610 A10 22219490 C T upstream_gene_variant MODIFIER c.-115G>A| S38
144961 BAA10g29610 A10 22220088 C T upstream_gene_variant MODIFIER c.-713G>A| S188
144962 BAA10g29610 A10 22220598 C T upstream_gene_variant MODIFIER c.-1223G>A| S306
S308
144963 BAA10g29620 A10 22226529 C T synonymous_variant LOW c.543C>T|p.Ile181Ile S168
144964 BAA10g29630 A10 22227337 C T upstream_gene_variant MODIFIER c.-2186C>T| S46
144965 BAA10g29620 A10 22227786 C T missense_variant MODERATE c.1250C>T|p.Ser417Phe S232
144966 BAA10g29630 A10 22228022 C T upstream_gene_variant MODIFIER c.-1501C>T| S96
144967 BAA10g29630 A10 22228555 C T upstream_gene_variant MODIFIER c.-968C>T| S9
144968 BAA10g29640 A10 22230140 G A upstream_gene_variant MODIFIER c.-1772G>A| S59
144969 BAA10g29640 A10 22230402 C T upstream_gene_variant MODIFIER c.-1510C>T| S161
144970 BAA10g29630 A10 22230695 G A missense_variant MODERATE c.553G>A|p.Glu185Lys S76
144971 BAA10g29630 A10 22230720 G A missense_variant MODERATE c.578G>A|p.Arg193Lys S53
144972 BAA10g29630 A10 22230756 C T missense_variant MODERATE c.614C>T|p.Ser205Phe S187
S188
S299
144973 BAA10g29630 A10 22230902 C T missense_variant MODERATE c.650C>T|p.Ala217Val S292
144974 BAA10g29640 A10 22232052 C T synonymous_variant LOW c.141C>T|p.Pro47Pro S78
144975 BAA10g29640 A10 22232819 G A missense_variant MODERATE c.719G>A|p.Gly240Glu S132
S137
S215