Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g19520 A05 11551044 G T downstream_gene_variant MODIFIER c.*1643C>A| S257
2 BAA05g19520 A05 11551132 G A downstream_gene_variant MODIFIER c.*1555C>T| S244
3 BAA05g19520 A05 11552700 G A missense_variant MODERATE c.1772C>T|p.Pro591Leu S64
4 BAA05g19520 A05 11552856 G A missense_variant MODERATE c.1616C>T|p.Thr539Ile S41
5 BAA05g19520 A05 11553124 C T missense_variant MODERATE c.1348G>A|p.Ala450Thr S36
6 BAA05g19520 A05 11553278 G A synonymous_variant LOW c.1194C>T|p.Pro398Pro S80
7 BAA05g19520 A05 11553353 G A synonymous_variant LOW c.1119C>T|p.Pro373Pro S249
8 BAA05g19520 A05 11553598 C T missense_variant MODERATE c.874G>A|p.Val292Ile S50
9 BAA05g19520 A05 11553813 G A missense_variant MODERATE c.659C>T|p.Pro220Leu S264
10 BAA05g19520 A05 11553837 G A missense_variant MODERATE c.635C>T|p.Ala212Val S203
11 BAA05g19520 A05 11554274 C T splice_donor_variant&intron_variant HIGH c.604+1G>A| S136
12 BAA05g19520 A05 11554434 C T splice_acceptor_variant&intron_variant HIGH c.446-1G>A| S174
13 BAA05g19520 A05 11554718 G A missense_variant MODERATE c.335C>T|p.Pro112Leu S134