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
136451 BAA10g22090 A10 19170472 G A upstream_gene_variant MODIFIER c.-4910G>A| S221
136452 BAA10g22090 A10 19171203 C T upstream_gene_variant MODIFIER c.-4179C>T| S262
136453 BAA10g22090 A10 19171819 G A upstream_gene_variant MODIFIER c.-3563G>A| S298
136454 BAA10g22090 A10 19172114 G A upstream_gene_variant MODIFIER c.-3268G>A| S11
S207
S224
S248
S271
S272
S40
S49
S71
136455 BAA10g22090 A10 19172428 G A upstream_gene_variant MODIFIER c.-2954G>A| S265
136456 BAA10g22090 A10 19172820 C T upstream_gene_variant MODIFIER c.-2562C>T| S282
136457 BAA10g22090 A10 19173538 G A upstream_gene_variant MODIFIER c.-1844G>A| S252
136458 BAA10g22090 A10 19174863 G A upstream_gene_variant MODIFIER c.-519G>A| S198
136459 BAA10g22090 A10 19176039 C T synonymous_variant LOW c.658C>T|p.Leu220Leu S83
S88
136460 BAA10g22090 A10 19176461 G A downstream_gene_variant MODIFIER c.*282G>A| S155
S211
136461 BAA10g22100 A10 19177429 G A missense_variant MODERATE c.238C>T|p.Pro80Ser S50
136462 BAA10g22100 A10 19179522 C T upstream_gene_variant MODIFIER c.-1054G>A| S235
136463 BAA10g22100 A10 19182157 G A upstream_gene_variant MODIFIER c.-3689C>T| S172
136464 BAA10g22110 A10 19183548 C T upstream_gene_variant MODIFIER c.-28C>T| S306
S308
136465 BAA10g22110 A10 19184843 C T missense_variant MODERATE c.671C>T|p.Ala224Val S96
136466 BAA10g22110 A10 19184921 G A missense_variant MODERATE c.749G>A|p.Ser250Asn S36
136467 BAA10g22110 A10 19185260 C T missense_variant MODERATE c.1088C>T|p.Thr363Ile S116
136468 BAA10g22120 A10 19185985 C A upstream_gene_variant MODIFIER c.-572C>A| S51
S92
136469 BAA10g22110 A10 19186874 G A downstream_gene_variant MODIFIER c.*1523G>A| S71
136470 BAA10g22110 A10 19187166 C T downstream_gene_variant MODIFIER c.*1815C>T| S244
136471 BAA10g22110 A10 19187463 C T downstream_gene_variant MODIFIER c.*2112C>T| S255
136472 BAA10g22120 A10 19189329 C T missense_variant MODERATE c.1298C>T|p.Ser433Leu S259
136473 BAA10g22120 A10 19189877 G A missense_variant MODERATE c.1547G>A|p.Gly516Glu S174
S27
136474 BAA10g22120 A10 19190107 G A missense_variant MODERATE c.1690G>A|p.Ala564Thr S62
136475 BAA10g22120 A10 19190856 C T stop_gained HIGH c.1921C>T|p.Gln641* S282