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
153401 BAA02g01890 A02 831365 G A upstream_gene_variant MODIFIER c.-2893C>T| S302
153402 BAA02g01900 A02 831997 C T missense_variant MODERATE c.1169C>T|p.Ser390Phe S174
153403 BAA02g01900 A02 832240 G A splice_acceptor_variant&intron_variant HIGH c.1216-1G>A| S302
153404 BAA02g01900 A02 832289 G A missense_variant MODERATE c.1264G>A|p.Asp422Asn S136
S305
153405 BAA02g01900 A02 833228 C T missense_variant MODERATE c.2131C>T|p.Leu711Phe S120
153406 BAA02g01900 A02 833340 C T missense_variant&splice_region_variant MODERATE c.2147C>T|p.Ala716Val S33
153407 BAA02g01900 A02 834708 C T synonymous_variant LOW c.2643C>T|p.Ile881Ile S255
153408 BAA02g01900 A02 836169 C T intron_variant MODIFIER c.3042+110C>T| S144
153409 BAA02g01900 A02 836900 G A intron_variant MODIFIER c.3186+37G>A| S59
153410 BAA02g01900 A02 837346 C T missense_variant MODERATE c.3314C>T|p.Ser1105Phe S218
153411 BAA02g01900 A02 837546 C T missense_variant MODERATE c.3377C>T|p.Ser1126Leu S81
S85
153412 BAA02g01900 A02 838163 G A missense_variant MODERATE c.3682G>A|p.Asp1228Asn S158
153413 BAA02g01900 A02 838463 C T intron_variant MODIFIER c.3844-56C>T| S16
153414 BAA02g01900 A02 839600 C T synonymous_variant LOW c.4413C>T|p.Pro1471Pro S179
153415 BAA02g01910 A02 839907 G A upstream_gene_variant MODIFIER c.-3833G>A| S217
S248
153416 BAA02g01910 A02 842976 G A upstream_gene_variant MODIFIER c.-764G>A| S163
153417 BAA02g01910 A02 843413 C T upstream_gene_variant MODIFIER c.-327C>T| S178
153418 BAA02g01900 A02 844617 G A downstream_gene_variant MODIFIER c.*3693G>A| S25
153419 BAA02g01920 A02 845692 C T upstream_gene_variant MODIFIER c.-4967C>T| S182
153420 BAA02g01920 A02 849140 G A upstream_gene_variant MODIFIER c.-1519G>A| S156
153421 BAA02g01910 A02 849229 G A synonymous_variant LOW c.2841G>A|p.Gln947Gln S23
153422 BAA02g01910 A02 851170 C T downstream_gene_variant MODIFIER c.*1151C>T| S142
153423 BAA02g01920 A02 851807 G A missense_variant MODERATE c.781G>A|p.Glu261Lys S50
153424 BAA02g01920 A02 851876 T A missense_variant MODERATE c.850T>A|p.Phe284Ile S73
S91
153425 BAA02g01920 A02 852093 G A missense_variant MODERATE c.977G>A|p.Gly326Glu S308