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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g66310 A09 60678756 C T upstream_gene_variant MODIFIER c.-2762C>T| S242
2 BAA09g66310 A09 60679648 C T upstream_gene_variant MODIFIER c.-1870C>T| S183
S198
3 BAA09g66310 A09 60680935 G A upstream_gene_variant MODIFIER c.-583G>A| S96
4 BAA09g66310 A09 60684014 C T synonymous_variant LOW c.1611C>T|p.Ser537Ser S236
5 BAA09g66310 A09 60684448 G A missense_variant MODERATE c.2045G>A|p.Ser682Asn S190
6 BAA09g66310 A09 60684852 C T synonymous_variant LOW c.2370C>T|p.Gly790Gly S138
7 BAA09g66310 A09 60685154 G A intron_variant MODIFIER c.2505+167G>A| S283
8 BAA09g66310 A09 60686765 C T missense_variant MODERATE c.3478C>T|p.Pro1160Ser S172
S217
9 BAA09g66310 A09 60686946 C T missense_variant MODERATE c.3659C>T|p.Ser1220Phe S279
10 BAA09g66310 A09 60686949 C T missense_variant MODERATE c.3662C>T|p.Pro1221Leu S50
11 BAA09g66310 A09 60686958 C T missense_variant MODERATE c.3671C>T|p.Ser1224Phe S156
12 BAA09g66310 A09 60687188 G A missense_variant MODERATE c.3901G>A|p.Glu1301Lys S211
13 BAA09g66310 A09 60687587 G A missense_variant MODERATE c.4156G>A|p.Ala1386Thr S2
14 BAA09g66310 A09 60688298 G A splice_region_variant&intron_variant LOW c.4603-4G>A| S36
15 BAA09g66310 A09 60688692 C T missense_variant MODERATE c.4904C>T|p.Pro1635Leu S259
16 BAA09g66310 A09 60688771 C T synonymous_variant LOW c.4983C>T|p.Asn1661Asn S6