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 BAA06g32960 A06 22277161 G A upstream_gene_variant MODIFIER c.-3459G>A| S292
2 BAA06g32960 A06 22277391 C T upstream_gene_variant MODIFIER c.-3229C>T| S148
3 BAA06g32960 A06 22279330 G A upstream_gene_variant MODIFIER c.-1290G>A| S20
4 BAA06g32960 A06 22282860 C T synonymous_variant LOW c.756C>T|p.Arg252Arg S42
5 BAA06g32960 A06 22284434 G A missense_variant MODERATE c.1958G>A|p.Ser653Asn S139
6 BAA06g32960 A06 22284917 C T missense_variant MODERATE c.2441C>T|p.Ser814Phe S303
7 BAA06g32960 A06 22285984 G A missense_variant MODERATE c.3062G>A|p.Arg1021Lys S183
S198
8 BAA06g32960 A06 22286283 G A missense_variant MODERATE c.3361G>A|p.Ala1121Thr S225
S73
9 BAA06g32960 A06 22286523 C T missense_variant MODERATE c.3601C>T|p.Pro1201Ser S232
10 BAA06g32960 A06 22286949 G A missense_variant MODERATE c.4027G>A|p.Gly1343Arg S284
11 BAA06g32960 A06 22287380 C T missense_variant MODERATE c.4340C>T|p.Ser1447Phe S128
12 BAA06g32960 A06 22289416 G A missense_variant MODERATE c.6292G>A|p.Glu2098Lys S140
13 BAA06g32960 A06 22289902 G A missense_variant MODERATE c.6778G>A|p.Ala2260Thr S12
14 BAA06g32960 A06 22290017 C T missense_variant MODERATE c.6893C>T|p.Thr2298Ile S132
S215