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
157401 BAA02g05100 A02 2239373 C T upstream_gene_variant MODIFIER c.-3767C>T| S180
157402 BAA02g05100 A02 2242338 G A upstream_gene_variant MODIFIER c.-802G>A| S308
157403 BAA02g05100 A02 2242438 G T upstream_gene_variant MODIFIER c.-702G>T| S289
157404 BAA02g05100 A02 2243240 C T missense_variant MODERATE c.101C>T|p.Pro34Leu S121
157405 BAA02g05110 A02 2243996 C T downstream_gene_variant MODIFIER c.*2506G>A| S230
157406 BAA02g05100 A02 2244742 C T missense_variant MODERATE c.725C>T|p.Thr242Ile S178
157407 BAA02g05100 A02 2245380 C T missense_variant MODERATE c.1141C>T|p.Pro381Ser S241
157408 BAA02g05100 A02 2245574 G A missense_variant MODERATE c.1258G>A|p.Gly420Ser S166
157409 BAA02g05100 A02 2245708 C T missense_variant MODERATE c.1304C>T|p.Ser435Phe S185
157410 BAA02g05110 A02 2246668 C T missense_variant MODERATE c.1019G>A|p.Gly340Glu S131
157411 BAA02g05100 A02 2247313 A T downstream_gene_variant MODIFIER c.*1038A>T| S231
157412 BAA02g05110 A02 2247422 C T missense_variant MODERATE c.829G>A|p.Ala277Thr S175
157413 BAA02g05110 A02 2247774 C T synonymous_variant LOW c.477G>A|p.Arg159Arg S211
S227
157414 BAA02g05110 A02 2248171 G A missense_variant MODERATE c.80C>T|p.Ala27Val S192
157415 BAA02g05110 A02 2248939 C T upstream_gene_variant MODIFIER c.-689G>A| S152
157416 BAA02g05110 A02 2251924 C T upstream_gene_variant MODIFIER c.-3674G>A| S73
157417 BAA02g05110 A02 2252021 C T upstream_gene_variant MODIFIER c.-3771G>A| S193
157418 BAA02g05120 A02 2254296 C T missense_variant MODERATE c.824C>T|p.Thr275Ile S202
157419 BAA02g05120 A02 2254314 C T missense_variant MODERATE c.842C>T|p.Ser281Phe S174
S265
S39
157420 BAA02g05120 A02 2254912 C T missense_variant MODERATE c.1345C>T|p.Leu449Phe S73
157421 BAA02g05120 A02 2255179 G A missense_variant MODERATE c.1612G>A|p.Gly538Ser S259
157422 BAA02g05130 A02 2256773 G A missense_variant MODERATE c.40G>A|p.Glu14Lys S256
157423 BAA02g05120 A02 2257381 G A downstream_gene_variant MODIFIER c.*2101G>A| S158
157424 BAA02g05130 A02 2258681 C T synonymous_variant LOW c.714C>T|p.Asn238Asn S19
157425 BAA02g05140 A02 2262629 G A upstream_gene_variant MODIFIER c.-668G>A| S163