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 BAA10g34800 A10 24344486 C T missense_variant MODERATE c.1597G>A|p.Asp533Asn S142
2 BAA10g34800 A10 24344999 G A missense_variant MODERATE c.1084C>T|p.Leu362Phe S260
3 BAA10g34800 A10 24345532 G A missense_variant MODERATE c.718C>T|p.Leu240Phe S209
4 BAA10g34800 A10 24345673 G A missense_variant MODERATE c.665C>T|p.Thr222Ile S15
S2
S3
S34
S4
S6
5 BAA10g34800 A10 24345884 C T synonymous_variant LOW c.537G>A|p.Glu179Glu S36
6 BAA10g34800 A10 24346318 G A synonymous_variant LOW c.510C>T|p.Leu170Leu S16
7 BAA10g34800 A10 24346424 G A missense_variant MODERATE c.404C>T|p.Ser135Phe S237
8 BAA10g34800 A10 24346948 C T upstream_gene_variant MODIFIER c.-121G>A| S136
9 BAA10g34800 A10 24346958 C T upstream_gene_variant MODIFIER c.-131G>A| S157
10 BAA10g34800 A10 24347813 T C upstream_gene_variant MODIFIER c.-986A>G| S212
11 BAA10g34800 A10 24349213 G A upstream_gene_variant MODIFIER c.-2386C>T| S94
12 BAA10g34800 A10 24350580 G A upstream_gene_variant MODIFIER c.-3753C>T| S264
13 BAA10g34800 A10 24351527 G A upstream_gene_variant MODIFIER c.-4700C>T| S64