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 BAA07g39360 A07 35330536 G A upstream_gene_variant MODIFIER c.-2903G>A| S302
2 BAA07g39360 A07 35331944 G A upstream_gene_variant MODIFIER c.-1495G>A| S166
3 BAA07g39360 A07 35332688 C T upstream_gene_variant MODIFIER c.-751C>T| S191
4 BAA07g39360 A07 35333450 G A synonymous_variant LOW c.12G>A|p.Glu4Glu S1
S90
5 BAA07g39360 A07 35333753 C T synonymous_variant LOW c.315C>T|p.Pro105Pro S77
S82
6 BAA07g39360 A07 35333780 G A synonymous_variant LOW c.342G>A|p.Lys114Lys S20
7 BAA07g39360 A07 35334420 G A missense_variant MODERATE c.860G>A|p.Arg287His S246
8 BAA07g39360 A07 35335292 C T missense_variant MODERATE c.1732C>T|p.Leu578Phe S299
9 BAA07g39360 A07 35335890 G A missense_variant MODERATE c.2330G>A|p.Ser777Asn S202
10 BAA07g39360 A07 35336204 G A missense_variant MODERATE c.2644G>A|p.Glu882Lys S152
11 BAA07g39360 A07 35336973 C T missense_variant MODERATE c.3413C>T|p.Ser1138Phe S301
S304
12 BAA07g39360 A07 35337528 C T missense_variant MODERATE c.3968C>T|p.Ser1323Phe S41
13 BAA07g39360 A07 35338433 C T splice_region_variant&intron_variant LOW c.4422+7C>T| S207