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 BAA05g32780 A05 34764106 G A missense_variant MODERATE c.5153C>T|p.Thr1718Ile S134
2 BAA05g32780 A05 34764150 G A synonymous_variant LOW c.5109C>T|p.Leu1703Leu S230
3 BAA05g32780 A05 34764360 G A synonymous_variant LOW c.4899C>T|p.Leu1633Leu S180
4 BAA05g32780 A05 34765347 C T splice_region_variant&intron_variant LOW c.4433-4G>A| S117
5 BAA05g32780 A05 34765659 C T missense_variant MODERATE c.4291G>A|p.Gly1431Ser S255
6 BAA05g32780 A05 34765704 G A synonymous_variant LOW c.4246C>T|p.Leu1416Leu S6
7 BAA05g32780 A05 34766628 G A intron_variant MODIFIER c.3718+10C>T| S159
8 BAA05g32780 A05 34766647 C T missense_variant MODERATE c.3709G>A|p.Asp1237Asn S193
9 BAA05g32780 A05 34768943 C T missense_variant MODERATE c.2322G>A|p.Met774Ile S198
10 BAA05g32780 A05 34769119 G A intron_variant MODIFIER c.2261-22C>T| S165
11 BAA05g32780 A05 34769962 C T stop_gained HIGH c.1761G>A|p.Trp587* S289
S290
12 BAA05g32780 A05 34770766 C T synonymous_variant LOW c.1440G>A|p.Gln480Gln S13
13 BAA05g32780 A05 34772021 C T splice_acceptor_variant&intron_variant HIGH c.670-1G>A| S2
14 BAA05g32780 A05 34773586 C T upstream_gene_variant MODIFIER c.-20G>A| S35
15 BAA05g32780 A05 34773652 G A upstream_gene_variant MODIFIER c.-86C>T| S256
16 BAA05g32780 A05 34774112 G A upstream_gene_variant MODIFIER c.-546C>T| S275
17 BAA05g32780 A05 34774568 C T upstream_gene_variant MODIFIER c.-1002G>A| S167
18 BAA05g32780 A05 34775051 G A upstream_gene_variant MODIFIER c.-1485C>T| S66
19 BAA05g32780 A05 34777345 G A upstream_gene_variant MODIFIER c.-3779C>T| S225
S73
20 BAA05g32780 A05 34777555 C T upstream_gene_variant MODIFIER c.-3989G>A| S292