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 BAA01g27510 A01 15948652 C T missense_variant MODERATE c.2128G>A|p.Ala710Thr S128
2 BAA01g27510 A01 15949550 C T splice_acceptor_variant&intron_variant HIGH c.1540-1G>A| S295
3 BAA01g27510 A01 15951516 C T missense_variant MODERATE c.259G>A|p.Val87Met S230
4 BAA01g27510 A01 15951671 G A synonymous_variant LOW c.195C>T|p.Leu65Leu S37
5 BAA01g27510 A01 15951706 C T missense_variant MODERATE c.160G>A|p.Glu54Lys S159
S234
6 BAA01g27510 A01 15952516 G A intron_variant MODIFIER c.92-742C>T| S56
7 BAA01g27510 A01 15953965 G A missense_variant MODERATE c.4C>T|p.Pro2Ser S294
8 BAA01g27510 A01 15954986 C T upstream_gene_variant MODIFIER c.-1018G>A| S206
9 BAA01g27510 A01 15955048 C T upstream_gene_variant MODIFIER c.-1080G>A| S282
10 BAA01g27510 A01 15956643 C T upstream_gene_variant MODIFIER c.-2675G>A| S125
11 BAA01g27510 A01 15957654 G A upstream_gene_variant MODIFIER c.-3686C>T| S122
S60
12 BAA01g27510 A01 15958280 G A upstream_gene_variant MODIFIER c.-4312C>T| S236
S260
13 BAA01g27510 A01 15958936 C T upstream_gene_variant MODIFIER c.-4968G>A| S39