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 BAA01g36500 A01 24437186 C T missense_variant MODERATE c.3290G>A|p.Gly1097Glu S298
2 BAA01g36500 A01 24437240 C T splice_acceptor_variant&intron_variant HIGH c.3237-1G>A| S242
3 BAA01g36500 A01 24437362 G A synonymous_variant LOW c.3201C>T|p.His1067His S221
4 BAA01g36500 A01 24437457 C T missense_variant MODERATE c.3106G>A|p.Val1036Met S164
5 BAA01g36500 A01 24437908 C T intron_variant MODIFIER c.2880-131G>A| S167
6 BAA01g36500 A01 24438602 G A missense_variant MODERATE c.2558C>T|p.Ser853Phe S35
7 BAA01g36500 A01 24440379 C T intron_variant MODIFIER c.1080-53G>A| S305
8 BAA01g36500 A01 24440605 G A missense_variant MODERATE c.1028C>T|p.Ser343Phe S5
9 BAA01g36500 A01 24441382 C T missense_variant MODERATE c.440G>A|p.Ser147Asn S166
10 BAA01g36500 A01 24442226 G A upstream_gene_variant MODIFIER c.-308C>T| S110
S262
11 BAA01g36500 A01 24445360 C T upstream_gene_variant MODIFIER c.-3442G>A| S249
12 BAA01g36500 A01 24446204 G A upstream_gene_variant MODIFIER c.-4286C>T| S197
13 BAA01g36500 A01 24446414 G A upstream_gene_variant MODIFIER c.-4496C>T| S299