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
52901 BAA01g29170 A01 18400164 C T missense_variant MODERATE c.1217G>A|p.Gly406Glu S182
52902 BAA01g29170 A01 18400367 C T missense_variant MODERATE c.1090G>A|p.Gly364Arg S94
52903 BAA01g29170 A01 18401787 C T upstream_gene_variant MODIFIER c.-283G>A| S272
52904 BAA01g29170 A01 18404552 C T upstream_gene_variant MODIFIER c.-3048G>A| S205
52905 BAA01g29170 A01 18405336 G A upstream_gene_variant MODIFIER c.-3832C>T| S74
52906 BAA01g29180 A01 18406629 G A downstream_gene_variant MODIFIER c.*4439C>T| S207
52907 BAA01g29180 A01 18407977 C T downstream_gene_variant MODIFIER c.*3091G>A| S200
52908 BAA01g29180 A01 18409580 G A downstream_gene_variant MODIFIER c.*1488C>T| S129
52909 BAA01g29180 A01 18410341 G A downstream_gene_variant MODIFIER c.*727C>T| S212
52910 BAA01g29180 A01 18410548 G A downstream_gene_variant MODIFIER c.*520C>T| S257
52911 BAA01g29180 A01 18411165 C T missense_variant MODERATE c.308G>A|p.Arg103Lys S270
52912 BAA01g29180 A01 18411170 C T synonymous_variant LOW c.303G>A|p.Lys101Lys S157
52913 BAA01g29180 A01 18411867 G A upstream_gene_variant MODIFIER c.-395C>T| S296
52914 BAA01g29190 A01 18413102 C T missense_variant MODERATE c.139G>A|p.Ala47Thr S271
52915 BAA01g29180 A01 18413262 G A upstream_gene_variant MODIFIER c.-1790C>T| S288
52916 BAA01g29200 A01 18414803 C T missense_variant MODERATE c.203G>A|p.Ser68Asn S170
52917 BAA01g29180 A01 18415626 C T upstream_gene_variant MODIFIER c.-4154G>A| S295
52918 BAA01g29180 A01 18415648 G A upstream_gene_variant MODIFIER c.-4176C>T| S124
52919 BAA01g29180 A01 18415914 C T upstream_gene_variant MODIFIER c.-4442G>A| S277
52920 BAA01g29180 A01 18415929 G A upstream_gene_variant MODIFIER c.-4457C>T| S168
52921 BAA01g29190 A01 18416932 C T upstream_gene_variant MODIFIER c.-3692G>A| S272
52922 BAA01g29210 A01 18418017 G A synonymous_variant LOW c.514C>T|p.Leu172Leu S36
52923 BAA01g29220 A01 18419445 C T missense_variant MODERATE c.763G>A|p.Gly255Arg S163
52924 BAA01g29220 A01 18419604 C T missense_variant MODERATE c.691G>A|p.Glu231Lys S166
S237
52925 BAA01g29220 A01 18419799 G A stop_gained HIGH c.496C>T|p.Gln166* S308