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
137451 BAA10g23060 A10 19582359 G A missense_variant MODERATE c.389C>T|p.Thr130Ile S279
137452 BAA10g23060 A10 19583325 C T missense_variant MODERATE c.50G>A|p.Gly17Glu S268
137453 BAA10g23050 A10 19583378 C T upstream_gene_variant MODIFIER c.-2205G>A| S177
137454 BAA10g23050 A10 19583397 G A upstream_gene_variant MODIFIER c.-2224C>T| S192
137455 BAA10g23050 A10 19583850 G A upstream_gene_variant MODIFIER c.-2677C>T| S288
137456 BAA10g23050 A10 19584462 C T upstream_gene_variant MODIFIER c.-3289G>A| S108
137457 BAA10g23050 A10 19584880 G A upstream_gene_variant MODIFIER c.-3707C>T| S128
137458 BAA10g23050 A10 19585415 G A upstream_gene_variant MODIFIER c.-4242C>T| S18
137459 BAA10g23070 A10 19586662 C T missense_variant MODERATE c.617C>T|p.Thr206Ile S161
137460 BAA10g23070 A10 19586782 C T missense_variant MODERATE c.737C>T|p.Ser246Phe S20
137461 BAA10g23080 A10 19588482 C T upstream_gene_variant MODIFIER c.-342G>A| S52
137462 BAA10g23090 A10 19588641 G A missense_variant MODERATE c.328C>T|p.Pro110Ser S223
137463 BAA10g23090 A10 19588742 G A missense_variant MODERATE c.227C>T|p.Pro76Leu S271
137464 BAA10g23080 A10 19589210 C T upstream_gene_variant MODIFIER c.-1070G>A| S150
137465 BAA10g23100 A10 19589360 T A stop_gained HIGH c.463A>T|p.Lys155* S97
137466 BAA10g23100 A10 19590066 C T splice_acceptor_variant&intron_variant HIGH c.73-1G>A| S10
137467 BAA10g23080 A10 19590780 C T upstream_gene_variant MODIFIER c.-2640G>A| S42
137468 BAA10g23110 A10 19591531 C T missense_variant MODERATE c.22C>T|p.Leu8Phe S236
137469 BAA10g23110 A10 19596176 G A synonymous_variant LOW c.327G>A|p.Glu109Glu S35
137470 BAA10g23120 A10 19597317 G A missense_variant MODERATE c.433G>A|p.Ala145Thr S164
137471 BAA10g23130 A10 19597559 C T upstream_gene_variant MODIFIER c.-1161C>T| S37
137472 BAA10g23130 A10 19598103 C T upstream_gene_variant MODIFIER c.-617C>T| S305
137473 BAA10g23130 A10 19598396 G A upstream_gene_variant MODIFIER c.-324G>A| S298
137474 BAA10g23130 A10 19598960 G A splice_region_variant&intron_variant LOW c.234+7G>A| S6
137475 BAA10g23140 A10 19599522 G A upstream_gene_variant MODIFIER c.-2786G>A| S75