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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g33910 A07 32605550 C T missense_variant MODERATE c.364C>T|p.Pro122Ser S56
2 BAA07g33910 A07 32606936 C T missense_variant MODERATE c.1630C>T|p.Pro544Ser S9
3 BAA07g33910 A07 32607129 G A intron_variant MODIFIER c.1689+134G>A| S183
S198
4 BAA07g33910 A07 32607144 G A intron_variant MODIFIER c.1689+149G>A| S295
5 BAA07g33910 A07 32607491 C T missense_variant MODERATE c.1814C>T|p.Ser605Leu S293
6 BAA07g33910 A07 32608571 C T missense_variant MODERATE c.2894C>T|p.Ser965Phe S177
7 BAA07g33910 A07 32608581 C T synonymous_variant LOW c.2904C>T|p.Asp968Asp S293
8 BAA07g33910 A07 32608667 G A missense_variant MODERATE c.2990G>A|p.Cys997Tyr S186
9 BAA07g33910 A07 32608675 C T missense_variant MODERATE c.2998C>T|p.Pro1000Ser S100
10 BAA07g33910 A07 32608735 G A missense_variant MODERATE c.3058G>A|p.Glu1020Lys S182
11 BAA07g33910 A07 32608852 C T stop_gained HIGH c.3175C>T|p.Gln1059* S108
12 BAA07g33910 A07 32608988 C T missense_variant MODERATE c.3311C>T|p.Pro1104Leu S138
13 BAA07g33910 A07 32609552 C T missense_variant MODERATE c.3875C>T|p.Thr1292Ile S138
14 BAA07g33910 A07 32609786 G A missense_variant MODERATE c.4109G>A|p.Arg1370Lys S139
15 BAA07g33910 A07 32609953 G A missense_variant MODERATE c.4276G>A|p.Val1426Ile S152
16 BAA07g33910 A07 32610163 G A missense_variant MODERATE c.4486G>A|p.Val1496Ile S295
17 BAA07g33910 A07 32610339 C T synonymous_variant LOW c.4662C>T|p.Phe1554Phe S201
18 BAA07g33910 A07 32610542 G A missense_variant MODERATE c.4865G>A|p.Arg1622Lys S13
19 BAA07g33910 A07 32610598 G A missense_variant MODERATE c.4921G>A|p.Asp1641Asn S130