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
135001 BAA10g21040 A10 18655583 C T upstream_gene_variant MODIFIER c.-2738G>A| S236
135002 BAA10g21040 A10 18656539 C T upstream_gene_variant MODIFIER c.-3694G>A| S162
S283
135003 BAA10g21040 A10 18656560 C T upstream_gene_variant MODIFIER c.-3715G>A| S165
135004 BAA10g21050 A10 18656628 C T missense_variant MODERATE c.2525C>T|p.Ser842Leu S189
135005 BAA10g21040 A10 18656715 C T upstream_gene_variant MODIFIER c.-3870G>A| S238
135006 BAA10g21050 A10 18657311 G A synonymous_variant LOW c.3120G>A|p.Leu1040Leu S63
135007 BAA10g21040 A10 18657402 C T upstream_gene_variant MODIFIER c.-4557G>A| S211
135008 BAA10g21040 A10 18657794 G A upstream_gene_variant MODIFIER c.-4949C>T| S3
135009 BAA10g21050 A10 18657859 C T downstream_gene_variant MODIFIER c.*461C>T| S45
135010 BAA10g21050 A10 18657898 C T downstream_gene_variant MODIFIER c.*500C>T| S199
135011 BAA10g21060 A10 18658401 G A synonymous_variant LOW c.3603C>T|p.Cys1201Cys S105
S106
135012 BAA10g21070 A10 18664248 C T upstream_gene_variant MODIFIER c.-2542C>T| S162
135013 BAA10g21060 A10 18665241 G A upstream_gene_variant MODIFIER c.-656C>T| S71
135014 BAA10g21060 A10 18665710 C T upstream_gene_variant MODIFIER c.-1125G>A| S238
135015 BAA10g21060 A10 18665954 C T upstream_gene_variant MODIFIER c.-1369G>A| S168
S219
S72
135016 BAA10g21060 A10 18667663 C T upstream_gene_variant MODIFIER c.-3078G>A| S20
135017 BAA10g21070 A10 18667733 G A missense_variant MODERATE c.272G>A|p.Arg91Lys S192
135018 BAA10g21070 A10 18667965 C T synonymous_variant LOW c.405C>T|p.Cys135Cys S107
135019 BAA10g21060 A10 18668114 C T upstream_gene_variant MODIFIER c.-3529G>A| S87
135020 BAA10g21070 A10 18668355 A C synonymous_variant LOW c.708A>C|p.Ile236Ile S157
S163
S249
S43
135021 BAA10g21070 A10 18668462 G A missense_variant MODERATE c.815G>A|p.Gly272Glu S69
135022 BAA10g21070 A10 18668770 G A missense_variant MODERATE c.1123G>A|p.Ala375Thr S27
135023 BAA10g21070 A10 18668993 G A missense_variant MODERATE c.1346G>A|p.Gly449Glu S270
135024 BAA10g21070 A10 18669485 G A missense_variant MODERATE c.1838G>A|p.Arg613Lys S279
135025 BAA10g21070 A10 18670806 G A splice_donor_variant&intron_variant HIGH c.2793+1G>A| S288