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
149901 BAA10g33960 A10 24033157 G A upstream_gene_variant MODIFIER c.-3955C>T| S197
149902 BAA10g33960 A10 24033230 G A upstream_gene_variant MODIFIER c.-4028C>T| S308
149903 BAA10g33960 A10 24033429 C T upstream_gene_variant MODIFIER c.-4227G>A| S169
S236
149904 BAA10g33960 A10 24033536 C T upstream_gene_variant MODIFIER c.-4334G>A| S269
149905 BAA10g33960 A10 24033537 G A upstream_gene_variant MODIFIER c.-4335C>T| S243
149906 BAA10g33960 A10 24033815 G A upstream_gene_variant MODIFIER c.-4613C>T| S180
149907 BAA10g33970 A10 24035115 C T downstream_gene_variant MODIFIER c.*2319G>A| S243
149908 BAA10g33970 A10 24035174 C T downstream_gene_variant MODIFIER c.*2260G>A| S142
149909 BAA10g33970 A10 24035290 C T downstream_gene_variant MODIFIER c.*2144G>A| S67
149910 BAA10g33970 A10 24035741 G A downstream_gene_variant MODIFIER c.*1693C>T| S7
149911 BAA10g33970 A10 24036340 G A downstream_gene_variant MODIFIER c.*1094C>T| S219
S72
149912 BAA10g33970 A10 24036744 C T downstream_gene_variant MODIFIER c.*690G>A| S202
149913 BAA10g33970 A10 24037378 C T downstream_gene_variant MODIFIER c.*56G>A| S208
S93
149914 BAA10g33970 A10 24037735 G A missense_variant MODERATE c.1220C>T|p.Ser407Phe S162
149915 BAA10g33970 A10 24037792 C T missense_variant MODERATE c.1163G>A|p.Ser388Asn S74
149916 BAA10g33970 A10 24039491 C T synonymous_variant LOW c.285G>A|p.Gln95Gln S103
149917 BAA10g33970 A10 24039953 G A missense_variant MODERATE c.175C>T|p.Pro59Ser S125
149918 BAA10g33970 A10 24040214 G A upstream_gene_variant MODIFIER c.-87C>T| S294
149919 BAA10g33970 A10 24043595 C T upstream_gene_variant MODIFIER c.-3468G>A| S103
149920 BAA10g33970 A10 24043982 C T upstream_gene_variant MODIFIER c.-3855G>A| S277
149921 BAA10g33980 A10 24046578 T C upstream_gene_variant MODIFIER c.-44A>G| S205
149922 BAA10g33980 A10 24046579 C T upstream_gene_variant MODIFIER c.-45G>A| S279
149923 BAA10g33980 A10 24047989 C T upstream_gene_variant MODIFIER c.-1455G>A| S165
149924 BAA10g33990 A10 24048518 G A missense_variant MODERATE c.268G>A|p.Val90Ile S298
149925 BAA10g33990 A10 24048664 G A splice_acceptor_variant&intron_variant HIGH c.326-1G>A| S202