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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g38550 A09 46339727 C T upstream_gene_variant MODIFIER c.-1125C>T| S144
2 BAA09g38550 A09 46340018 C T upstream_gene_variant MODIFIER c.-834C>T| S19
3 BAA09g38550 A09 46340631 G A upstream_gene_variant MODIFIER c.-221G>A| S151
S263
4 BAA09g38550 A09 46340860 G A synonymous_variant LOW c.9G>A|p.Glu3Glu S10
5 BAA09g38550 A09 46341278 G A missense_variant MODERATE c.244G>A|p.Glu82Lys S231
6 BAA09g38550 A09 46341403 G A synonymous_variant LOW c.369G>A|p.Glu123Glu S45
7 BAA09g38550 A09 46342162 C T synonymous_variant LOW c.1128C>T|p.Leu376Leu S260
8 BAA09g38550 A09 46343056 C T synonymous_variant LOW c.2022C>T|p.Leu674Leu S138
9 BAA09g38550 A09 46343260 G A synonymous_variant LOW c.2226G>A|p.Glu742Glu S221
10 BAA09g38550 A09 46343279 C T stop_gained HIGH c.2245C>T|p.Gln749* S37
11 BAA09g38550 A09 46343489 G A missense_variant MODERATE c.2455G>A|p.Glu819Lys S246
12 BAA09g38550 A09 46343743 G A synonymous_variant LOW c.2709G>A|p.Gln903Gln S202
13 BAA09g38550 A09 46343931 C T missense_variant MODERATE c.2897C>T|p.Ser966Leu S94
14 BAA09g38550 A09 46346235 G A missense_variant MODERATE c.4795G>A|p.Glu1599Lys S4
S70
15 BAA09g38550 A09 46350131 C T downstream_gene_variant MODIFIER c.*3022C>T| S108