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


Gene ID

Results: 1 - 38 of 38 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g15280 A02 7324026 C T downstream_gene_variant MODIFIER c.*4918G>A| S77
S82
2 BAA02g15280 A02 7324549 G C downstream_gene_variant MODIFIER c.*4395C>G| S41
3 BAA02g15280 A02 7325341 C T downstream_gene_variant MODIFIER c.*3603G>A| S25
4 BAA02g15280 A02 7325608 G A downstream_gene_variant MODIFIER c.*3336C>T| S166
5 BAA02g15280 A02 7327696 C T downstream_gene_variant MODIFIER c.*1248G>A| S252
6 BAA02g15280 A02 7328084 G A downstream_gene_variant MODIFIER c.*860C>T| S59
7 BAA02g15280 A02 7328621 C T downstream_gene_variant MODIFIER c.*323G>A| S186
8 BAA02g15280 A02 7328762 G A downstream_gene_variant MODIFIER c.*182C>T| S295
9 BAA02g15280 A02 7329347 C T missense_variant MODERATE c.3314G>A|p.Arg1105Lys S205
10 BAA02g15280 A02 7329749 G A missense_variant MODERATE c.2912C>T|p.Ala971Val S204
11 BAA02g15280 A02 7329774 G A missense_variant MODERATE c.2887C>T|p.His963Tyr S279
12 BAA02g15280 A02 7330086 G A missense_variant MODERATE c.2575C>T|p.His859Tyr S47
13 BAA02g15280 A02 7330996 G A intron_variant MODIFIER c.2352-687C>T| S41
14 BAA02g15280 A02 7331139 G A intron_variant MODIFIER c.2351+647C>T| S109
15 BAA02g15280 A02 7331339 G A intron_variant MODIFIER c.2351+447C>T| S105
16 BAA02g15280 A02 7331340 C T intron_variant MODIFIER c.2351+446G>A| S9
17 BAA02g15280 A02 7331576 G A intron_variant MODIFIER c.2351+210C>T| S265
18 BAA02g15280 A02 7331649 T C intron_variant MODIFIER c.2351+137A>G| S32
19 BAA02g15280 A02 7331755 G A intron_variant MODIFIER c.2351+31C>T| S45
20 BAA02g15280 A02 7331802 C T missense_variant MODERATE c.2335G>A|p.Glu779Lys S88
21 BAA02g15280 A02 7331996 C T missense_variant MODERATE c.2141G>A|p.Arg714Lys S242
22 BAA02g15280 A02 7332011 C T missense_variant MODERATE c.2126G>A|p.Gly709Glu S273
23 BAA02g15280 A02 7332035 C T missense_variant MODERATE c.2102G>A|p.Ser701Asn S123
S278
24 BAA02g15280 A02 7332390 G A intron_variant MODIFIER c.1828-81C>T| S45
25 BAA02g15280 A02 7332522 C T intron_variant MODIFIER c.1828-213G>A| S25