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
136401 BAA10g22060 A10 19149987 G A downstream_gene_variant MODIFIER c.*345G>A| S160
136402 BAA10g22060 A10 19154021 C T downstream_gene_variant MODIFIER c.*4379C>T| S45
136403 BAA10g22060-BAA10g22070 A10 19155724 G A intergenic_region MODIFIER n.19155724G>A| S43
136404 BAA10g22060-BAA10g22070 A10 19157266 G A intergenic_region MODIFIER n.19157266G>A| S178
136405 BAA10g22060-BAA10g22070 A10 19158109 G A intergenic_region MODIFIER n.19158109G>A| S105
S106
136406 BAA10g22070 A10 19159245 C T upstream_gene_variant MODIFIER c.-4302C>T| S291
136407 BAA10g22070 A10 19160561 G A upstream_gene_variant MODIFIER c.-2986G>A| S212
136408 BAA10g22070 A10 19160855 G A upstream_gene_variant MODIFIER c.-2692G>A| S16
136409 BAA10g22070 A10 19162008 C T upstream_gene_variant MODIFIER c.-1539C>T| S119
136410 BAA10g22070 A10 19162332 C T upstream_gene_variant MODIFIER c.-1215C>T| S257
136411 BAA10g22070 A10 19162931 C T upstream_gene_variant MODIFIER c.-616C>T| S269
136412 BAA10g22080 A10 19163967 C T upstream_gene_variant MODIFIER c.-4865C>T| S143
136413 BAA10g22080 A10 19166569 C T upstream_gene_variant MODIFIER c.-2263C>T| S229
136414 BAA10g22080 A10 19166613 C T upstream_gene_variant MODIFIER c.-2219C>T| S148
S210
S30
S31
136415 BAA10g22080 A10 19167247 G A upstream_gene_variant MODIFIER c.-1585G>A| S166
136416 BAA10g22080 A10 19167502 G A upstream_gene_variant MODIFIER c.-1330G>A| S117
136417 BAA10g22080 A10 19167507 G A upstream_gene_variant MODIFIER c.-1325G>A| S288
136418 BAA10g22080 A10 19168136 G A upstream_gene_variant MODIFIER c.-696G>A| S263
136419 BAA10g22080 A10 19168318 C T upstream_gene_variant MODIFIER c.-514C>T| S169
136420 BAA10g22070 A10 19169013 G A downstream_gene_variant MODIFIER c.*3958G>A| S4
136421 BAA10g22070 A10 19169018 C T downstream_gene_variant MODIFIER c.*3963C>T| S103
136422 BAA10g22080 A10 19169764 G A missense_variant MODERATE c.158G>A|p.Gly53Glu S273
136423 BAA10g22080 A10 19170159 C T intron_variant MODIFIER c.371-17C>T| S150
136424 BAA10g22080 A10 19170358 G A downstream_gene_variant MODIFIER c.*94G>A| S178
136425 BAA10g22080 A10 19170371 C T downstream_gene_variant MODIFIER c.*107C>T| S206
S26