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
179501 BAA02g19840 A02 10416488 C T downstream_gene_variant MODIFIER c.*938G>A| S163
179502 BAA02g19840 A02 10419906 C T intron_variant MODIFIER c.657-448G>A| S292
179503 BAA02g19840 A02 10420185 C T intron_variant MODIFIER c.656+257G>A| S8
179504 BAA02g19840 A02 10420314 C T intron_variant MODIFIER c.656+128G>A| S202
179505 BAA02g19840 A02 10420338 C T intron_variant MODIFIER c.656+104G>A| S218
179506 BAA02g19840 A02 10422728 C T upstream_gene_variant MODIFIER c.-1463G>A| S289
S290
179507 BAA02g19840 A02 10424114 G A upstream_gene_variant MODIFIER c.-2849C>T| S200
179508 BAA02g19840 A02 10424508 C T upstream_gene_variant MODIFIER c.-3243G>A| S301
S304
179509 BAA02g19840 A02 10425276 A C upstream_gene_variant MODIFIER c.-4011T>G| S55
179510 BAA02g19840 A02 10425530 G A upstream_gene_variant MODIFIER c.-4265C>T| S12
179511 BAA02g19840 A02 10425837 C T upstream_gene_variant MODIFIER c.-4572G>A| S275
179512 BAA02g19850 A02 10426581 C T upstream_gene_variant MODIFIER c.-3052C>T| S167
179513 BAA02g19850 A02 10427352 G A upstream_gene_variant MODIFIER c.-2281G>A| S206
S26
179514 BAA02g19850 A02 10429925 G A missense_variant MODERATE c.220G>A|p.Ala74Thr S134
179515 BAA02g19850 A02 10430385 C T synonymous_variant LOW c.471C>T|p.Ile157Ile S77
S82
179516 BAA02g19850 A02 10430386 C T stop_gained HIGH c.472C>T|p.Arg158* S183
S198
179517 BAA02g19850 A02 10431108 C T missense_variant MODERATE c.865C>T|p.His289Tyr S73
179518 BAA02g19850 A02 10432249 C T intron_variant MODIFIER c.882-251C>T| S255
179519 BAA02g19850 A02 10432414 C T intron_variant MODIFIER c.882-86C>T| S250
179520 BAA02g19850 A02 10432834 C T missense_variant MODERATE c.1216C>T|p.Leu406Phe S219
S72
179521 BAA02g19850 A02 10434662 C T downstream_gene_variant MODIFIER c.*1253C>T| S105
S106
179522 BAA02g19860 A02 10438880 G A intron_variant MODIFIER c.2194+98C>T| S59
179523 BAA02g19860 A02 10439305 C T missense_variant MODERATE c.1867G>A|p.Gly623Ser S171
179524 BAA02g19860 A02 10439324 G A synonymous_variant LOW c.1848C>T|p.Asn616Asn S296
179525 BAA02g19860 A02 10440366 G A intron_variant MODIFIER c.1690+19C>T| S11