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
22751 BAA01g16480 A01 8010963 G A missense_variant MODERATE c.914C>T|p.Ser305Leu S165
22752 BAA01g16480 A01 8011181 C T synonymous_variant LOW c.696G>A|p.Leu232Leu S18
22753 BAA01g16480 A01 8011255 G A missense_variant MODERATE c.622C>T|p.Arg208Cys S293
22754 BAA01g16480 A01 8011345 C T missense_variant MODERATE c.532G>A|p.Asp178Asn S50
22755 BAA01g16480 A01 8011491 G A missense_variant MODERATE c.386C>T|p.Ser129Phe S110
22756 BAA01g16490 A01 8011829 C T upstream_gene_variant MODIFIER c.-1892C>T| S9
22757 BAA01g16480 A01 8012095 C T synonymous_variant LOW c.189G>A|p.Glu63Glu S264
22758 BAA01g16480 A01 8012177 G A missense_variant MODERATE c.107C>T|p.Ala36Val S162
22759 BAA01g16480 A01 8012293 C T upstream_gene_variant MODIFIER c.-10G>A| S284
22760 BAA01g16490 A01 8014026 G A missense_variant MODERATE c.306G>A|p.Met102Ile S287
22761 BAA01g16490 A01 8014213 G A missense_variant MODERATE c.493G>A|p.Ala165Thr S241
22762 BAA01g16480 A01 8014932 G A upstream_gene_variant MODIFIER c.-2649C>T| S183
22763 BAA01g16500 A01 8016321 C T missense_variant MODERATE c.2020G>A|p.Ala674Thr S306
S308
22764 BAA01g16500 A01 8017173 G A missense_variant MODERATE c.1610C>T|p.Ser537Phe S249
22765 BAA01g16500 A01 8017259 C T splice_region_variant&intron_variant LOW c.1528-4G>A| S185
22766 BAA01g16500 A01 8017887 G A missense_variant MODERATE c.1184C>T|p.Ser395Phe S139
22767 BAA01g16490 A01 8018472 G A downstream_gene_variant MODIFIER c.*3804G>A| S84
S93
22768 BAA01g16490 A01 8019158 C T downstream_gene_variant MODIFIER c.*4490C>T| S252
22769 BAA01g16500 A01 8020702 C T missense_variant MODERATE c.224G>A|p.Ser75Asn S20
22770 BAA01g16500 A01 8021173 G A stop_gained HIGH c.100C>T|p.Gln34* S293
22771 BAA01g16500 A01 8021565 G A upstream_gene_variant MODIFIER c.-293C>T| S8
22772 BAA01g16500 A01 8021794 G A upstream_gene_variant MODIFIER c.-522C>T| S142
22773 BAA01g16500 A01 8022501 C T upstream_gene_variant MODIFIER c.-1229G>A| S275
22774 BAA01g16500 A01 8023240 G A upstream_gene_variant MODIFIER c.-1968C>T| S124
22775 BAA01g16500 A01 8023261 G A upstream_gene_variant MODIFIER c.-1989C>T| S56