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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g19120 A05 11171459 G A upstream_gene_variant MODIFIER c.-3715G>A| S104
S52
2 BAA05g19120 A05 11171671 G A upstream_gene_variant MODIFIER c.-3503G>A| S308
3 BAA05g19120 A05 11172575 C T upstream_gene_variant MODIFIER c.-2599C>T| S44
4 BAA05g19120 A05 11172622 C T upstream_gene_variant MODIFIER c.-2552C>T| S17
5 BAA05g19120 A05 11175324 C T missense_variant MODERATE c.151C>T|p.Pro51Ser S295
6 BAA05g19120 A05 11177504 G A missense_variant MODERATE c.1684G>A|p.Ala562Thr S283
7 BAA05g19120 A05 11178098 C T stop_gained HIGH c.2278C>T|p.Gln760* S198
8 BAA05g19120 A05 11179585 C T missense_variant MODERATE c.2647C>T|p.Pro883Ser S105
9 BAA05g19120 A05 11179618 G A missense_variant MODERATE c.2680G>A|p.Ala894Thr S78
10 BAA05g19120 A05 11179721 C T missense_variant MODERATE c.2783C>T|p.Pro928Leu S103
11 BAA05g19120 A05 11179820 C T missense_variant MODERATE c.2882C>T|p.Ser961Phe S117
12 BAA05g19120 A05 11180101 G A missense_variant MODERATE c.3163G>A|p.Glu1055Lys S23
13 BAA05g19120 A05 11180215 C T missense_variant MODERATE c.3277C>T|p.Pro1093Ser S262
14 BAA05g19120 A05 11180743 C T missense_variant MODERATE c.3805C>T|p.Leu1269Phe S295
15 BAA05g19120 A05 11181018 C T missense_variant MODERATE c.3986C>T|p.Ala1329Val S232
16 BAA05g19120 A05 11181463 C T synonymous_variant LOW c.4305C>T|p.Asn1435Asn S153
S213
17 BAA05g19120 A05 11183086 C T synonymous_variant LOW c.5133C>T|p.Ser1711Ser S198
18 BAA05g19120 A05 11183181 C T missense_variant MODERATE c.5228C>T|p.Ser1743Phe S164
19 BAA05g19120 A05 11183649 C T missense_variant MODERATE c.5401C>T|p.Pro1801Ser S256
20 BAA05g19120 A05 11183799 C T missense_variant MODERATE c.5551C>T|p.Pro1851Ser S246