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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g42050 A09 48589070 G A synonymous_variant LOW c.282G>A|p.Glu94Glu S156
2 BAA09g42050 A09 48589698 C T missense_variant MODERATE c.712C>T|p.Leu238Phe S20
3 BAA09g42050 A09 48589939 C T missense_variant MODERATE c.953C>T|p.Thr318Ile S292
4 BAA09g42050 A09 48590140 C T missense_variant MODERATE c.1154C>T|p.Pro385Leu S55
5 BAA09g42050 A09 48590184 C T missense_variant MODERATE c.1198C>T|p.Pro400Ser S174
6 BAA09g42050 A09 48591376 G A intron_variant MODIFIER c.1356+344G>A| S107
7 BAA09g42050 A09 48591542 G A intron_variant MODIFIER c.1356+510G>A| S271
S79
8 BAA09g42050 A09 48591748 C T intron_variant MODIFIER c.1356+716C>T| S245
9 BAA09g42050 A09 48592000 C T intron_variant MODIFIER c.1357-488C>T| S303
10 BAA09g42050 A09 48592369 G A intron_variant MODIFIER c.1357-119G>A| S231
11 BAA09g42050 A09 48592940 T G synonymous_variant LOW c.1629T>G|p.Ala543Ala S153
S205
S235
S250
12 BAA09g42050 A09 48593202 C T missense_variant MODERATE c.1891C>T|p.Leu631Phe S186
13 BAA09g42050 A09 48593411 C T synonymous_variant LOW c.2100C>T|p.Asn700Asn S114
14 BAA09g42050 A09 48593649 C T missense_variant MODERATE c.2338C>T|p.His780Tyr S257