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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g31850 A10 23116029 G A downstream_gene_variant MODIFIER c.*3026C>T| S273
2 BAA10g31850 A10 23116474 G A downstream_gene_variant MODIFIER c.*2581C>T| S239
3 BAA10g31850 A10 23117023 G A downstream_gene_variant MODIFIER c.*2032C>T| S178
4 BAA10g31850 A10 23117449 C T downstream_gene_variant MODIFIER c.*1606G>A| S116
S123
5 BAA10g31850 A10 23119266 C T missense_variant MODERATE c.2228G>A|p.Arg743Lys S211
S227
6 BAA10g31850 A10 23119936 C T synonymous_variant LOW c.1737G>A|p.Thr579Thr S262
7 BAA10g31850 A10 23120630 C T missense_variant MODERATE c.1043G>A|p.Arg348Lys S229
8 BAA10g31850 A10 23121540 C T missense_variant MODERATE c.683G>A|p.Gly228Glu S176
9 BAA10g31850 A10 23121595 G A missense_variant MODERATE c.628C>T|p.Pro210Ser S265
10 BAA10g31850 A10 23122151 G A missense_variant MODERATE c.304C>T|p.Leu102Phe S216
11 BAA10g31850 A10 23122246 G A missense_variant MODERATE c.280C>T|p.Pro94Ser S65
12 BAA10g31850 A10 23122343 G A synonymous_variant LOW c.183C>T|p.Asp61Asp S240
13 BAA10g31850 A10 23122430 G A synonymous_variant LOW c.96C>T|p.His32His S84
S93
14 BAA10g31850 A10 23124393 C T upstream_gene_variant MODIFIER c.-1868G>A| S203