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 BAA10g25720 A10 20660568 G A missense_variant MODERATE c.307G>A|p.Glu103Lys S255
2 BAA10g25720 A10 20660656 G A missense_variant MODERATE c.395G>A|p.Gly132Glu S176
3 BAA10g25720 A10 20660724 G A missense_variant MODERATE c.463G>A|p.Val155Ile S120
4 BAA10g25720 A10 20661363 C T missense_variant MODERATE c.983C>T|p.Pro328Leu S243
5 BAA10g25720 A10 20661798 G A missense_variant MODERATE c.1418G>A|p.Cys473Tyr S207
6 BAA10g25720 A10 20661813 C T missense_variant MODERATE c.1433C>T|p.Ser478Leu S153
S213
7 BAA10g25720 A10 20661837 C T missense_variant MODERATE c.1457C>T|p.Ser486Phe S189
8 BAA10g25720 A10 20662434 G A missense_variant MODERATE c.2054G>A|p.Gly685Glu S143
9 BAA10g25720 A10 20662609 G A synonymous_variant LOW c.2229G>A|p.Gly743Gly S64
10 BAA10g25720 A10 20663345 G A missense_variant MODERATE c.2965G>A|p.Glu989Lys S205
11 BAA10g25720 A10 20663557 G A synonymous_variant LOW c.3177G>A|p.Gly1059Gly S4
12 BAA10g25720 A10 20666602 G A downstream_gene_variant MODIFIER c.*2096G>A| S53
13 BAA10g25720 A10 20668472 C T downstream_gene_variant MODIFIER c.*3966C>T| S166