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 BAA01g13990 A01 6651493 A G upstream_gene_variant MODIFIER c.-4861A>G| S115
2 BAA01g13990 A01 6656501 G A missense_variant MODERATE c.148G>A|p.Val50Met S129
3 BAA01g13990 A01 6656933 C T synonymous_variant LOW c.492C>T|p.Gly164Gly S80
4 BAA01g13990 A01 6657702 G A missense_variant MODERATE c.1261G>A|p.Gly421Ser S105
S106
5 BAA01g13990 A01 6658000 C T missense_variant MODERATE c.1492C>T|p.His498Tyr S249
6 BAA01g13990 A01 6659019 G A synonymous_variant LOW c.2511G>A|p.Arg837Arg S122
7 BAA01g13990 A01 6659224 G A missense_variant MODERATE c.2716G>A|p.Asp906Asn S8
8 BAA01g13990 A01 6659341 G A missense_variant MODERATE c.2833G>A|p.Asp945Asn S110
9 BAA01g13990 A01 6659367 C T synonymous_variant LOW c.2859C>T|p.Phe953Phe S226
10 BAA01g13990 A01 6659630 C T missense_variant MODERATE c.3122C>T|p.Ser1041Phe S158
11 BAA01g13990 A01 6661470 C T synonymous_variant LOW c.3579C>T|p.Arg1193Arg S2
12 BAA01g13990 A01 6661509 T C synonymous_variant LOW c.3618T>C|p.Arg1206Arg S235
13 BAA01g13990 A01 6661542 C T synonymous_variant LOW c.3651C>T|p.Leu1217Leu S132
S137
14 BAA01g13990 A01 6664376 C T downstream_gene_variant MODIFIER c.*2807C>T| S249
15 BAA01g13990 A01 6666528 G A downstream_gene_variant MODIFIER c.*4959G>A| S96