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 BAA02g42210 A02 35187318 C T missense_variant MODERATE c.463C>T|p.Pro155Ser S98
2 BAA02g42210 A02 35187734 C T missense_variant MODERATE c.673C>T|p.Pro225Ser S182
3 BAA02g42210 A02 35188134 G A synonymous_variant LOW c.876G>A|p.Val292Val S4
4 BAA02g42210 A02 35190496 C T intron_variant MODIFIER c.1830+11C>T| S239
5 BAA02g42210 A02 35191708 G A missense_variant MODERATE c.2275G>A|p.Ala759Thr S159
S243
6 BAA02g42210 A02 35191902 G A synonymous_variant LOW c.2469G>A|p.Gln823Gln S25
7 BAA02g42210 A02 35192061 C T synonymous_variant LOW c.2556C>T|p.Asn852Asn S47
S50
S51
S74
S85
8 BAA02g42210 A02 35192959 C T missense_variant MODERATE c.3454C>T|p.Pro1152Ser S165
9 BAA02g42210 A02 35193793 C T synonymous_variant LOW c.4209C>T|p.Tyr1403Tyr S98
10 BAA02g42210 A02 35194072 G A synonymous_variant LOW c.4488G>A|p.Arg1496Arg S233
11 BAA02g42210 A02 35195599 G A downstream_gene_variant MODIFIER c.*583G>A| S103
12 BAA02g42210 A02 35196013 G A downstream_gene_variant MODIFIER c.*997G>A| S35
13 BAA02g42210 A02 35197932 C T downstream_gene_variant MODIFIER c.*2916C>T| S211
14 BAA02g42210 A02 35198165 C T downstream_gene_variant MODIFIER c.*3149C>T| S234
15 BAA02g42210 A02 35199694 C T downstream_gene_variant MODIFIER c.*4678C>T| S202
16 BAA02g42210 A02 35199969 G A downstream_gene_variant MODIFIER c.*4953G>A| S159
S243