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 BAA10g20590 A10 18451879 C T upstream_gene_variant MODIFIER c.-1688C>T| S274
2 BAA10g20590 A10 18452874 G A upstream_gene_variant MODIFIER c.-693G>A| S162
3 BAA10g20590 A10 18453626 C T splice_region_variant&intron_variant LOW c.56+4C>T| S117
4 BAA10g20590 A10 18454027 A C missense_variant MODERATE c.319A>C|p.Thr107Pro S111
S152
S236
S308
S68
5 BAA10g20590 A10 18454666 G A missense_variant MODERATE c.958G>A|p.Asp320Asn S198
6 BAA10g20590 A10 18454852 G A missense_variant MODERATE c.1144G>A|p.Glu382Lys S272
7 BAA10g20590 A10 18455423 C T missense_variant MODERATE c.1628C>T|p.Ser543Phe S204
8 BAA10g20590 A10 18455486 G A missense_variant MODERATE c.1691G>A|p.Gly564Asp S16
S92
9 BAA10g20590 A10 18455515 G A missense_variant MODERATE c.1720G>A|p.Asp574Asn S139
10 BAA10g20590 A10 18455584 G A missense_variant MODERATE c.1789G>A|p.Asp597Asn S35
11 BAA10g20590 A10 18456381 G A downstream_gene_variant MODIFIER c.*168G>A| S178
12 BAA10g20590 A10 18456450 G A downstream_gene_variant MODIFIER c.*237G>A| S263
13 BAA10g20590 A10 18456809 C T downstream_gene_variant MODIFIER c.*596C>T| S10
14 BAA10g20590 A10 18457702 G A downstream_gene_variant MODIFIER c.*1489G>A| S265
15 BAA10g20590 A10 18458555 C T downstream_gene_variant MODIFIER c.*2342C>T| S266
16 BAA10g20590 A10 18458762 C T downstream_gene_variant MODIFIER c.*2549C>T| S194
17 BAA10g20590 A10 18458958 C T downstream_gene_variant MODIFIER c.*2745C>T| S25