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 BAA01g11790 A01 5489569 C T downstream_gene_variant MODIFIER c.*561G>A| S46
2 BAA01g11790 A01 5489873 C T downstream_gene_variant MODIFIER c.*257G>A| S2
3 BAA01g11790 A01 5490461 C T synonymous_variant LOW c.930G>A|p.Gln310Gln S17
S19
4 BAA01g11790 A01 5490473 C T splice_region_variant&synonymous_variant LOW c.918G>A|p.Gly306Gly S148
S210
S30
S31
5 BAA01g11790 A01 5490496 C T intron_variant MODIFIER c.917-22G>A| S204
6 BAA01g11790 A01 5490577 G A intron_variant MODIFIER c.917-103C>T| S45
7 BAA01g11790 A01 5491228 G A missense_variant MODERATE c.698C>T|p.Pro233Leu S257
8 BAA01g11790 A01 5492203 G A missense_variant MODERATE c.290C>T|p.Ser97Phe S32
9 BAA01g11790 A01 5492867 G A missense_variant MODERATE c.74C>T|p.Pro25Leu S54
10 BAA01g11790 A01 5492883 C T missense_variant MODERATE c.58G>A|p.Gly20Arg S46
11 BAA01g11790 A01 5494706 G A upstream_gene_variant MODIFIER c.-1766C>T| S114
12 BAA01g11790 A01 5495678 G A upstream_gene_variant MODIFIER c.-2738C>T| S127
13 BAA01g11790 A01 5496032 C T upstream_gene_variant MODIFIER c.-3092G>A| S36