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
121351 BAA10g12280-BAA10g12290 A10 13734670 G A intergenic_region MODIFIER n.13734670G>A| S95
121352 BAA10g12280-BAA10g12290 A10 13734857 C T intergenic_region MODIFIER n.13734857C>T| S131
121353 BAA10g12290 A10 13735596 C T upstream_gene_variant MODIFIER c.-4754C>T| S151
S263
121354 BAA10g12290 A10 13735774 C T upstream_gene_variant MODIFIER c.-4576C>T| S123
121355 BAA10g12290 A10 13735944 G A upstream_gene_variant MODIFIER c.-4406G>A| S74
121356 BAA10g12290 A10 13737243 C T upstream_gene_variant MODIFIER c.-3107C>T| S180
121357 BAA10g12290 A10 13737960 C T upstream_gene_variant MODIFIER c.-2390C>T| S183
121358 BAA10g12290 A10 13738727 G A upstream_gene_variant MODIFIER c.-1623G>A| S72
121359 BAA10g12290 A10 13739592 G A upstream_gene_variant MODIFIER c.-758G>A| S82
S92
121360 BAA10g12290 A10 13739738 G A upstream_gene_variant MODIFIER c.-612G>A| S95
121361 BAA10g12290 A10 13739976 G A upstream_gene_variant MODIFIER c.-374G>A| S208
121362 BAA10g12290 A10 13740306 C T upstream_gene_variant MODIFIER c.-44C>T| S225
S73
121363 BAA10g12290 A10 13741167 G A missense_variant MODERATE c.469G>A|p.Gly157Arg S163
121364 BAA10g12290 A10 13741258 C T missense_variant MODERATE c.560C>T|p.Pro187Leu S210
S225
121365 BAA10g12290 A10 13741285 G A missense_variant MODERATE c.587G>A|p.Gly196Asp S250
121366 BAA10g12300 A10 13743321 G A missense_variant MODERATE c.3229C>T|p.Pro1077Ser S57
121367 BAA10g12290 A10 13744057 G A downstream_gene_variant MODIFIER c.*2158G>A| S290
121368 BAA10g12290 A10 13744819 C T downstream_gene_variant MODIFIER c.*2920C>T| S25
121369 BAA10g12300 A10 13744974 C T missense_variant MODERATE c.2339G>A|p.Gly780Glu S63
121370 BAA10g12300 A10 13745479 G A missense_variant MODERATE c.1927C>T|p.Leu643Phe S280
121371 BAA10g12300 A10 13747971 G A intron_variant MODIFIER c.754+24C>T| S216
121372 BAA10g12300 A10 13748285 G A intron_variant MODIFIER c.663+54C>T| S192
121373 BAA10g12300 A10 13748438 G A synonymous_variant LOW c.564C>T|p.Thr188Thr S295
121374 BAA10g12300 A10 13748994 C T missense_variant&splice_region_variant MODERATE c.298G>A|p.Asp100Asn S40
S49
121375 BAA10g12300 A10 13749253 C T synonymous_variant LOW c.126G>A|p.Leu42Leu S187