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
95501 BAA10g04130-BAA10g04140 A10 2037267 G A intergenic_region MODIFIER n.2037267G>A| S107
95502 BAA10g04130-BAA10g04140 A10 2037354 C T intergenic_region MODIFIER n.2037354C>T| S15
S156
S2
S3
S34
95503 BAA10g04130-BAA10g04140 A10 2037372 G A intergenic_region MODIFIER n.2037372G>A| S245
95504 BAA10g04130-BAA10g04140 A10 2037568 C T intergenic_region MODIFIER n.2037568C>T| S224
95505 BAA10g04130-BAA10g04140 A10 2037627 G A intergenic_region MODIFIER n.2037627G>A| S236
95506 BAA10g04130-BAA10g04140 A10 2037972 C T intergenic_region MODIFIER n.2037972C>T| S35
95507 BAA10g04130-BAA10g04140 A10 2038190 C T intergenic_region MODIFIER n.2038190C>T| S190
95508 BAA10g04130-BAA10g04140 A10 2038217 C T intergenic_region MODIFIER n.2038217C>T| S84
95509 BAA10g04130-BAA10g04140 A10 2039109 C T intergenic_region MODIFIER n.2039109C>T| S305
95510 BAA10g04130-BAA10g04140 A10 2039145 C T intergenic_region MODIFIER n.2039145C>T| S183
95511 BAA10g04130-BAA10g04140 A10 2039351 C T intergenic_region MODIFIER n.2039351C>T| S256
95512 BAA10g04130-BAA10g04140 A10 2040225 C T intergenic_region MODIFIER n.2040225C>T| S169
S173
95513 BAA10g04130-BAA10g04140 A10 2041080 A T intergenic_region MODIFIER n.2041080A>T| S216
95514 BAA10g04140 A10 2041959 C T downstream_gene_variant MODIFIER c.*4183G>A| S229
95515 BAA10g04140 A10 2042358 G A downstream_gene_variant MODIFIER c.*3784C>T| S262
95516 BAA10g04140 A10 2043403 G A downstream_gene_variant MODIFIER c.*2739C>T| S1
95517 BAA10g04140 A10 2043862 G A downstream_gene_variant MODIFIER c.*2280C>T| S71
95518 BAA10g04140 A10 2043868 G A downstream_gene_variant MODIFIER c.*2274C>T| S172
95519 BAA10g04140 A10 2044819 C T downstream_gene_variant MODIFIER c.*1323G>A| S206
S26
95520 BAA10g04140 A10 2045507 G A downstream_gene_variant MODIFIER c.*635C>T| S292
95521 BAA10g04140 A10 2046280 C T synonymous_variant LOW c.879G>A|p.Leu293Leu S116
95522 BAA10g04140 A10 2046462 G A synonymous_variant LOW c.697C>T|p.Leu233Leu S46
95523 BAA10g04150 A10 2054266 C T intron_variant MODIFIER c.241-59C>T| S297
95524 BAA10g04150 A10 2054301 G A intron_variant MODIFIER c.241-24G>A| S242
95525 BAA10g04150 A10 2054784 G A downstream_gene_variant MODIFIER c.*379G>A| S36