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
169001 BAA02g14140 A02 6638507 C T upstream_gene_variant MODIFIER c.-2793G>A| S65
169002 BAA02g14150 A02 6639554 G A missense_variant MODERATE c.70G>A|p.Asp24Asn S280
169003 BAA02g14150 A02 6640020 C T missense_variant MODERATE c.536C>T|p.Ser179Phe S270
169004 BAA02g14140 A02 6640441 G A upstream_gene_variant MODIFIER c.-4727C>T| S206
169005 BAA02g14150 A02 6640913 C T synonymous_variant LOW c.810C>T|p.Ser270Ser S165
169006 BAA02g14150 A02 6641067 G A missense_variant MODERATE c.964G>A|p.Gly322Arg S202
169007 BAA02g14150 A02 6641190 A C missense_variant MODERATE c.1087A>C|p.Ser363Arg S137
S175
S221
S222
S234
S259
S286
S5
S97
169008 BAA02g14150 A02 6641322 C T missense_variant MODERATE c.1219C>T|p.Pro407Ser S178
169009 BAA02g14150 A02 6641436 G A missense_variant MODERATE c.1333G>A|p.Glu445Lys S122
169010 BAA02g14160 A02 6645698 C T upstream_gene_variant MODIFIER c.-1718G>A| S84
S93
169011 BAA02g14160 A02 6646131 C T upstream_gene_variant MODIFIER c.-2151G>A| S87
169012 BAA02g14160 A02 6646648 G A upstream_gene_variant MODIFIER c.-2668C>T| S278
169013 BAA02g14160 A02 6647294 C T upstream_gene_variant MODIFIER c.-3314G>A| S218
169014 BAA02g14180 A02 6648678 G A synonymous_variant LOW c.249C>T|p.Asp83Asp S28
169015 BAA02g14180 A02 6649006 G A upstream_gene_variant MODIFIER c.-80C>T| S164
169016 BAA02g14180 A02 6649076 G A upstream_gene_variant MODIFIER c.-150C>T| S34
169017 BAA02g14180 A02 6649877 C T upstream_gene_variant MODIFIER c.-951G>A| S131
169018 BAA02g14190 A02 6652237 C T missense_variant MODERATE c.313C>T|p.Pro105Ser S1
S90
169019 BAA02g14190 A02 6652297 G A missense_variant MODERATE c.373G>A|p.Gly125Ser S210
S225
169020 BAA02g14180 A02 6652657 C T upstream_gene_variant MODIFIER c.-3731G>A| S208
S219
169021 BAA02g14220 A02 6654311 C A upstream_gene_variant MODIFIER c.-4015C>A| S16
169022 BAA02g14200 A02 6654728 C T missense_variant MODERATE c.806C>T|p.Ser269Phe S301
S304
169023 BAA02g14200 A02 6655086 C T synonymous_variant LOW c.1164C>T|p.Ser388Ser S42
169024 BAA02g14210 A02 6656948 G A synonymous_variant LOW c.567C>T|p.Ile189Ile S45
169025 BAA02g14220 A02 6658426 C T missense_variant MODERATE c.101C>T|p.Pro34Leu S299