Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g36390 A01 24386707 G A downstream_gene_variant MODIFIER c.*2967C>T| S226
2 BAA01g36390 A01 24386755 C T downstream_gene_variant MODIFIER c.*2919G>A| S275
3 BAA01g36390 A01 24386776 C T downstream_gene_variant MODIFIER c.*2898G>A| S107
4 BAA01g36390 A01 24388842 G A downstream_gene_variant MODIFIER c.*832C>T| S246
5 BAA01g36390 A01 24389193 G A downstream_gene_variant MODIFIER c.*481C>T| S244
6 BAA01g36390 A01 24389488 G A downstream_gene_variant MODIFIER c.*186C>T| S181
7 BAA01g36390 A01 24389619 C T downstream_gene_variant MODIFIER c.*55G>A| S256
8 BAA01g36390 A01 24390170 G A missense_variant MODERATE c.1823C>T|p.Ala608Val S20
9 BAA01g36390 A01 24391086 C T missense_variant MODERATE c.1429G>A|p.Gly477Ser S183
S198
10 BAA01g36390 A01 24391413 C T splice_acceptor_variant&intron_variant HIGH c.1285-1G>A| S32
11 BAA01g36390 A01 24391543 G T missense_variant MODERATE c.1251C>A|p.Asn417Lys S117
S124
S148
S172
S210
S286
S298
S8
12 BAA01g36390 A01 24391828 C T missense_variant MODERATE c.1103G>A|p.Arg368Lys S39
13 BAA01g36390 A01 24391851 C T synonymous_variant LOW c.1080G>A|p.Glu360Glu S120
14 BAA01g36390 A01 24393447 C T missense_variant MODERATE c.322G>A|p.Glu108Lys S264
15 BAA01g36390 A01 24394043 C T missense_variant MODERATE c.25G>A|p.Glu9Lys S208
16 BAA01g36390 A01 24396977 C T upstream_gene_variant MODIFIER c.-2910G>A| S98
17 BAA01g36390 A01 24397540 G A upstream_gene_variant MODIFIER c.-3473C>T| S199