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
169551 BAA02g14660 A02 6854601 C T upstream_gene_variant MODIFIER c.-4761G>A| S40
S49
169552 BAA02g14670 A02 6855837 G A stop_gained HIGH c.210G>A|p.Trp70* S244
169553 BAA02g14670 A02 6856481 G A missense_variant MODERATE c.761G>A|p.Arg254Lys S45
169554 BAA02g14670 A02 6857293 G A missense_variant MODERATE c.1487G>A|p.Gly496Glu S264
169555 BAA02g14690 A02 6857597 G A upstream_gene_variant MODIFIER c.-1311G>A| S129
169556 BAA02g14690 A02 6857754 G A upstream_gene_variant MODIFIER c.-1154G>A| S69
169557 BAA02g14690 A02 6857819 G A upstream_gene_variant MODIFIER c.-1089G>A| S45
169558 BAA02g14690 A02 6858151 A C upstream_gene_variant MODIFIER c.-757A>C| S199
169559 BAA02g14680 A02 6858768 G A upstream_gene_variant MODIFIER c.-5C>T| S250
169560 BAA02g14680 A02 6858801 G A upstream_gene_variant MODIFIER c.-38C>T| S100
169561 BAA02g14680 A02 6859515 G A upstream_gene_variant MODIFIER c.-752C>T| S37
169562 BAA02g14690 A02 6859848 G A splice_region_variant&intron_variant LOW c.204-7G>A| S168
169563 BAA02g14690 A02 6860038 C T synonymous_variant LOW c.387C>T|p.Leu129Leu S276
169564 BAA02g14690 A02 6860306 G A missense_variant MODERATE c.655G>A|p.Ala219Thr S170
S207
169565 BAA02g14690 A02 6860378 G A missense_variant MODERATE c.727G>A|p.Asp243Asn S177
169566 BAA02g14680 A02 6860930 C T upstream_gene_variant MODIFIER c.-2167G>A| S87
169567 BAA02g14680 A02 6860988 G A upstream_gene_variant MODIFIER c.-2225C>T| S286
169568 BAA02g14680 A02 6862007 C T upstream_gene_variant MODIFIER c.-3244G>A| S306
S308
169569 BAA02g14680 A02 6863117 C T upstream_gene_variant MODIFIER c.-4354G>A| S289
S290
169570 BAA02g14680 A02 6863333 G T upstream_gene_variant MODIFIER c.-4570C>A| S50
169571 BAA02g14680 A02 6863396 C T upstream_gene_variant MODIFIER c.-4633G>A| S15
S3
169572 BAA02g14690 A02 6863913 C T intron_variant MODIFIER c.1415-400C>T| S13
169573 BAA02g14690 A02 6864057 C T intron_variant MODIFIER c.1415-256C>T| S162
169574 BAA02g14690 A02 6864203 C T intron_variant MODIFIER c.1415-110C>T| S18
169575 BAA02g14690 A02 6864480 C T downstream_gene_variant MODIFIER c.*82C>T| S58