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
154901 BAA02g03110 A02 1371278 C T missense_variant MODERATE c.311C>T|p.Ser104Phe S79
S84
154902 BAA02g03100 A02 1371326 C T upstream_gene_variant MODIFIER c.-1440G>A| S245
154903 BAA02g03120 A02 1372378 G A synonymous_variant LOW c.906C>T|p.Pro302Pro S221
154904 BAA02g03100 A02 1372523 C T upstream_gene_variant MODIFIER c.-2637G>A| S283
154905 BAA02g03120 A02 1372975 G A missense_variant MODERATE c.494C>T|p.Ala165Val S288
154906 BAA02g03120 A02 1373203 C T synonymous_variant LOW c.354G>A|p.Ser118Ser S183
S198
154907 BAA02g03120 A02 1373347 C T synonymous_variant LOW c.210G>A|p.Arg70Arg S180
154908 BAA02g03120 A02 1373500 G A synonymous_variant LOW c.57C>T|p.Leu19Leu S246
154909 BAA02g03100 A02 1373786 G A upstream_gene_variant MODIFIER c.-3900C>T| S244
154910 BAA02g03100 A02 1373910 C T upstream_gene_variant MODIFIER c.-4024G>A| S179
154911 BAA02g03100 A02 1374124 G A upstream_gene_variant MODIFIER c.-4238C>T| S244
154912 BAA02g03140 A02 1379268 G A upstream_gene_variant MODIFIER c.-2032G>A| S204
154913 BAA02g03130 A02 1379853 G A missense_variant MODERATE c.212C>T|p.Ala71Val S168
154914 BAA02g03130 A02 1379899 C T missense_variant MODERATE c.166G>A|p.Glu56Lys S174
S175
154915 BAA02g03130 A02 1380212 G A upstream_gene_variant MODIFIER c.-148C>T| S269
154916 BAA02g03130 A02 1380390 C T upstream_gene_variant MODIFIER c.-326G>A| S54
154917 BAA02g03130 A02 1380466 G A upstream_gene_variant MODIFIER c.-402C>T| S236
154918 BAA02g03130 A02 1380475 C T upstream_gene_variant MODIFIER c.-411G>A| S200
154919 BAA02g03130 A02 1381530 G A upstream_gene_variant MODIFIER c.-1466C>T| S45
154920 BAA02g03130 A02 1381625 G A upstream_gene_variant MODIFIER c.-1561C>T| S125
154921 BAA02g03130 A02 1382221 G A upstream_gene_variant MODIFIER c.-2157C>T| S86
154922 BAA02g03130 A02 1382694 C T upstream_gene_variant MODIFIER c.-2630G>A| S287
154923 BAA02g03130 A02 1383117 G A upstream_gene_variant MODIFIER c.-3053C>T| S210
154924 BAA02g03130 A02 1383768 G A upstream_gene_variant MODIFIER c.-3704C>T| S289
154925 BAA02g03130 A02 1383990 G A upstream_gene_variant MODIFIER c.-3926C>T| S95