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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g56100 A03 27743326 G A upstream_gene_variant MODIFIER c.-2321G>A| S287
2 BAA03g56100 A03 27745776 G A missense_variant MODERATE c.130G>A|p.Glu44Lys S272
3 BAA03g56100 A03 27746689 C T missense_variant MODERATE c.1043C>T|p.Thr348Met S110
4 BAA03g56100 A03 27746779 G A missense_variant MODERATE c.1133G>A|p.Ser378Asn S47
5 BAA03g56100 A03 27746801 C T synonymous_variant LOW c.1155C>T|p.Pro385Pro S59
6 BAA03g56100 A03 27746878 C T missense_variant MODERATE c.1232C>T|p.Thr411Ile S163
7 BAA03g56100 A03 27747052 G A missense_variant MODERATE c.1406G>A|p.Gly469Asp S165
8 BAA03g56100 A03 27747160 C T missense_variant MODERATE c.1514C>T|p.Ser505Phe S33
9 BAA03g56100 A03 27747463 G A missense_variant MODERATE c.1817G>A|p.Arg606His S296
10 BAA03g56100 A03 27747888 G A missense_variant MODERATE c.2078G>A|p.Gly693Glu S257
11 BAA03g56100 A03 27747913 G A synonymous_variant LOW c.2103G>A|p.Arg701Arg S112
12 BAA03g56100 A03 27748102 C T synonymous_variant LOW c.2292C>T|p.Tyr764Tyr S126
13 BAA03g56100 A03 27748348 C T synonymous_variant LOW c.2538C>T|p.Val846Val S140
14 BAA03g56100 A03 27748437 G A missense_variant MODERATE c.2627G>A|p.Gly876Glu S167
15 BAA03g56100 A03 27751050 C T downstream_gene_variant MODIFIER c.*2211C>T| S40
S49
16 BAA03g56100 A03 27751251 C T downstream_gene_variant MODIFIER c.*2412C>T| S256