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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g22770 A08 17035314 G A missense_variant MODERATE c.2918C>T|p.Ala973Val S190
2 BAA08g22770 A08 17035384 C T missense_variant MODERATE c.2848G>A|p.Glu950Lys S223
3 BAA08g22770 A08 17035651 G A missense_variant MODERATE c.2581C>T|p.Leu861Phe S155
S211
4 BAA08g22770 A08 17035905 C T missense_variant MODERATE c.2327G>A|p.Gly776Glu S166
5 BAA08g22770 A08 17036009 C T synonymous_variant LOW c.2223G>A|p.Glu741Glu S174
6 BAA08g22770 A08 17036237 C T synonymous_variant LOW c.1995G>A|p.Glu665Glu S230
7 BAA08g22770 A08 17037027 C T missense_variant MODERATE c.1205G>A|p.Ser402Asn S63
8 BAA08g22770 A08 17037067 C T missense_variant MODERATE c.1165G>A|p.Asp389Asn S90
9 BAA08g22770 A08 17037302 G A synonymous_variant LOW c.930C>T|p.Cys310Cys S42
10 BAA08g22770 A08 17037357 G A missense_variant MODERATE c.875C>T|p.Ser292Phe S72
S78
11 BAA08g22770 A08 17038230 G A missense_variant MODERATE c.74C>T|p.Ser25Phe S5
12 BAA08g22770 A08 17038254 G A missense_variant MODERATE c.50C>T|p.Ser17Phe S41
13 BAA08g22770 A08 17039395 C T upstream_gene_variant MODIFIER c.-1092G>A| S249
14 BAA08g22770 A08 17039688 C T upstream_gene_variant MODIFIER c.-1385G>A| S277
15 BAA08g22770 A08 17039717 C T upstream_gene_variant MODIFIER c.-1414G>A| S143
16 BAA08g22770 A08 17039935 T A upstream_gene_variant MODIFIER c.-1632A>T| S236
17 BAA08g22770 A08 17041470 C T upstream_gene_variant MODIFIER c.-3167G>A| S252