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
15051 BAA01g11640 A01 5392825 C T splice_region_variant&intron_variant LOW c.200+3C>T| S296
15052 BAA01g11640 A01 5392865 G T intron_variant MODIFIER c.201-38G>T| S298
15053 BAA01g11640 A01 5393551 C T synonymous_variant LOW c.693C>T|p.Ile231Ile S158
15054 BAA01g11640 A01 5393677 C T synonymous_variant LOW c.819C>T|p.Ile273Ile S58
15055 BAA01g11640 A01 5394352 C T missense_variant MODERATE c.1199C>T|p.Thr400Ile S184
15056 BAA01g11640 A01 5395662 C T downstream_gene_variant MODIFIER c.*1016C>T| S148
S30
S31
15057 BAA01g11640 A01 5396022 C T downstream_gene_variant MODIFIER c.*1376C>T| S130
15058 BAA01g11640 A01 5396248 C T downstream_gene_variant MODIFIER c.*1602C>T| S192
15059 BAA01g11640 A01 5398255 C T downstream_gene_variant MODIFIER c.*3609C>T| S98
15060 BAA01g11640 A01 5398908 G A downstream_gene_variant MODIFIER c.*4262G>A| S15
15061 BAA01g11650 A01 5399208 C T missense_variant&splice_region_variant MODERATE c.163G>A|p.Glu55Lys S265
15062 BAA01g11650 A01 5400035 G A upstream_gene_variant MODIFIER c.-262C>T| S159
S243
15063 BAA01g11650 A01 5403350 G A upstream_gene_variant MODIFIER c.-3577C>T| S15
15064 BAA01g11650 A01 5404207 C T upstream_gene_variant MODIFIER c.-4434G>A| S299
15065 BAA01g11650 A01 5404709 C T upstream_gene_variant MODIFIER c.-4936G>A| S264
15066 BAA01g11650 A01 5404731 G A upstream_gene_variant MODIFIER c.-4958C>T| S45
15067 BAA01g11670 A01 5404845 C T missense_variant MODERATE c.76C>T|p.Pro26Ser S20
15068 BAA01g11660 A01 5405180 C T upstream_gene_variant MODIFIER c.-758G>A| S242
15069 BAA01g11670 A01 5405277 G A missense_variant MODERATE c.293G>A|p.Gly98Asp S293
15070 BAA01g11670 A01 5405648 C T missense_variant MODERATE c.664C>T|p.Pro222Ser S64
15071 BAA01g11670 A01 5405897 G A missense_variant MODERATE c.791G>A|p.Gly264Glu S218
15072 BAA01g11670 A01 5405991 C T synonymous_variant LOW c.885C>T|p.Pro295Pro S231
15073 BAA01g11660 A01 5407093 T A upstream_gene_variant MODIFIER c.-2671A>T| S298
15074 BAA01g11680 A01 5408749 C T synonymous_variant LOW c.555G>A|p.Arg185Arg S278
15075 BAA01g11670 A01 5409660 C T downstream_gene_variant MODIFIER c.*3633C>T| S136