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
161251 BAA02g08430 A02 3601185 C T splice_region_variant&intron_variant LOW c.1242+4C>T| S15
S3
161252 BAA02g08410 A02 3601886 C T upstream_gene_variant MODIFIER c.-4795G>A| S73
161253 BAA02g08410 A02 3602067 G A upstream_gene_variant MODIFIER c.-4976C>T| S210
161254 BAA02g08440 A02 3602508 C T upstream_gene_variant MODIFIER c.-1524C>T| S292
161255 BAA02g08440 A02 3602846 C T upstream_gene_variant MODIFIER c.-1186C>T| S286
161256 BAA02g08440 A02 3602861 C T upstream_gene_variant MODIFIER c.-1171C>T| S195
161257 BAA02g08440 A02 3604277 C T synonymous_variant LOW c.246C>T|p.Ser82Ser S292
161258 BAA02g08440 A02 3604505 G A synonymous_variant LOW c.474G>A|p.Lys158Lys S5
161259 BAA02g08450 A02 3605110 C T upstream_gene_variant MODIFIER c.-4279C>T| S138
161260 BAA02g08440 A02 3607381 C T missense_variant MODERATE c.1631C>T|p.Ser544Phe S72
S78
161261 BAA02g08440 A02 3608017 C T missense_variant MODERATE c.2051C>T|p.Pro684Leu S276
161262 BAA02g08450 A02 3608356 G A upstream_gene_variant MODIFIER c.-1033G>A| S283
161263 BAA02g08450 A02 3609725 C T missense_variant MODERATE c.227C>T|p.Thr76Ile S216
161264 BAA02g08440 A02 3610287 C T downstream_gene_variant MODIFIER c.*1975C>T| S241
161265 BAA02g08460 A02 3611761 C T missense_variant MODERATE c.491G>A|p.Arg164Lys S287
161266 BAA02g08460 A02 3612728 G A upstream_gene_variant MODIFIER c.-143C>T| S10
161267 BAA02g08460 A02 3612893 G A upstream_gene_variant MODIFIER c.-308C>T| S89
161268 BAA02g08460 A02 3614841 G A upstream_gene_variant MODIFIER c.-2256C>T| S286
161269 BAA02g08470 A02 3615133 C T synonymous_variant LOW c.447G>A|p.Lys149Lys S255
161270 BAA02g08460 A02 3615823 G A upstream_gene_variant MODIFIER c.-3238C>T| S291
161271 BAA02g08480 A02 3618770 G A missense_variant MODERATE c.494C>T|p.Ala165Val S87
161272 BAA02g08480 A02 3618962 C T missense_variant MODERATE c.302G>A|p.Arg101His S202
161273 BAA02g08480 A02 3618982 A C synonymous_variant LOW c.282T>G|p.Arg94Arg S132
S135
S192
S202
S213
S215
S238
S295
S37
S69
161274 BAA02g08470 A02 3620488 C T upstream_gene_variant MODIFIER c.-4667G>A| S274
161275 BAA02g08470 A02 3620547 G A upstream_gene_variant MODIFIER c.-4726C>T| S263