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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g35200 A05 35967071 C T downstream_gene_variant MODIFIER c.*3668G>A| S139
2 BAA05g35200 A05 35968778 G A downstream_gene_variant MODIFIER c.*1961C>T| S128
3 BAA05g35200 A05 35968865 C T downstream_gene_variant MODIFIER c.*1874G>A| S8
4 BAA05g35200 A05 35968926 C T downstream_gene_variant MODIFIER c.*1813G>A| S298
5 BAA05g35200 A05 35969466 G A downstream_gene_variant MODIFIER c.*1273C>T| S252
6 BAA05g35200 A05 35970125 C T downstream_gene_variant MODIFIER c.*614G>A| S188
7 BAA05g35200 A05 35970512 G A downstream_gene_variant MODIFIER c.*227C>T| S177
8 BAA05g35200 A05 35971216 G A synonymous_variant LOW c.3778C>T|p.Leu1260Leu S138
9 BAA05g35200 A05 35971975 C T missense_variant MODERATE c.3562G>A|p.Glu1188Lys S237
10 BAA05g35200 A05 35973112 C T missense_variant MODERATE c.3184G>A|p.Gly1062Arg S132
S137
S215
11 BAA05g35200 A05 35974204 G A missense_variant MODERATE c.2378C>T|p.Ala793Val S226
12 BAA05g35200 A05 35974714 C T missense_variant MODERATE c.1868G>A|p.Gly623Asp S1
S90
13 BAA05g35200 A05 35975186 G A missense_variant MODERATE c.1396C>T|p.Pro466Ser S85
14 BAA05g35200 A05 35977814 C T synonymous_variant LOW c.57G>A|p.Ala19Ala S155
S211
15 BAA05g35200 A05 35977864 C T missense_variant MODERATE c.7G>A|p.Ala3Thr S58
16 BAA05g35200 A05 35982575 G A upstream_gene_variant MODIFIER c.-4705C>T| S18