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 BAA09g11300 A09 6352654 G A missense_variant MODERATE c.148G>A|p.Gly50Arg S128
2 BAA09g11300 A09 6352656 G A synonymous_variant LOW c.150G>A|p.Gly50Gly S159
S299
3 BAA09g11300 A09 6352770 G A missense_variant MODERATE c.264G>A|p.Met88Ile S246
4 BAA09g11300 A09 6352792 G A missense_variant MODERATE c.286G>A|p.Val96Ile S91
5 BAA09g11300 A09 6352800 G A synonymous_variant LOW c.294G>A|p.Lys98Lys S91
6 BAA09g11300 A09 6352803 C T synonymous_variant LOW c.297C>T|p.His99His S268
S91
7 BAA09g11300 A09 6352809 T A synonymous_variant LOW c.303T>A|p.Gly101Gly S91
8 BAA09g11300 A09 6352812 G A synonymous_variant LOW c.306G>A|p.Pro102Pro S91
9 BAA09g11300 A09 6352819 C T missense_variant MODERATE c.313C>T|p.Leu105Phe S91
10 BAA09g11300 A09 6352821 C G synonymous_variant LOW c.315C>G|p.Leu105Leu S91
11 BAA09g11300 A09 6352851 C T synonymous_variant LOW c.345C>T|p.Asn115Asn S91
12 BAA09g11300 A09 6352866 C T synonymous_variant LOW c.360C>T|p.Phe120Phe S91
13 BAA09g11300 A09 6352872 C T synonymous_variant LOW c.366C>T|p.Cys122Cys S91