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 BAA01g20690 A01 10219508 C T synonymous_variant LOW c.1608G>A|p.Glu536Glu S135
S185
S203
2 BAA01g20690 A01 10219882 G A synonymous_variant LOW c.1440C>T|p.Leu480Leu S202
3 BAA01g20690 A01 10220583 C T splice_acceptor_variant&intron_variant HIGH c.1033-1G>A| S42
4 BAA01g20690 A01 10220838 C T missense_variant&splice_region_variant MODERATE c.961G>A|p.Asp321Asn S200
5 BAA01g20690 A01 10221995 C T missense_variant MODERATE c.313G>A|p.Gly105Arg S143
6 BAA01g20690 A01 10222556 T A upstream_gene_variant MODIFIER c.-249A>T| S1
S90
7 BAA01g20690 A01 10222615 C T upstream_gene_variant MODIFIER c.-308G>A| S130
8 BAA01g20690 A01 10223130 C T upstream_gene_variant MODIFIER c.-823G>A| S270
9 BAA01g20690 A01 10223333 G A upstream_gene_variant MODIFIER c.-1026C>T| S211
S227
10 BAA01g20690 A01 10225886 G A upstream_gene_variant MODIFIER c.-3579C>T| S246
11 BAA01g20690 A01 10226164 C T upstream_gene_variant MODIFIER c.-3857G>A| S104
S184
12 BAA01g20690 A01 10226758 G A upstream_gene_variant MODIFIER c.-4451C>T| S209
13 BAA01g20690 A01 10226884 C T upstream_gene_variant MODIFIER c.-4577G>A| S158