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


Gene ID

Results: 1 - 30 of 30 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g34880 A02 30003819 G A upstream_gene_variant MODIFIER c.-371G>A| S134
2 BAA02g34880 A02 30004305 G A missense_variant MODERATE c.116G>A|p.Gly39Asp S72
S78
3 BAA02g34880 A02 30004562 G A missense_variant MODERATE c.373G>A|p.Val125Ile S58
4 BAA02g34880 A02 30004601 G A missense_variant MODERATE c.412G>A|p.Glu138Lys S280
5 BAA02g34880 A02 30004608 G A stop_gained HIGH c.419G>A|p.Trp140* S17
6 BAA02g34880 A02 30004686 C T missense_variant MODERATE c.497C>T|p.Thr166Ile S242
7 BAA02g34880 A02 30004729 C T synonymous_variant LOW c.540C>T|p.Thr180Thr S116
8 BAA02g34880 A02 30005328 G A missense_variant MODERATE c.1139G>A|p.Gly380Glu S10
9 BAA02g34880 A02 30005404 C T synonymous_variant LOW c.1215C>T|p.Asn405Asn S107
10 BAA02g34880 A02 30005490 C T missense_variant MODERATE c.1301C>T|p.Ala434Val S257
11 BAA02g34880 A02 30005614 G A synonymous_variant LOW c.1425G>A|p.Gly475Gly S136
12 BAA02g34880 A02 30005621 C T stop_gained HIGH c.1432C>T|p.Gln478* S179
13 BAA02g34880 A02 30006121 G A missense_variant MODERATE c.1799G>A|p.Gly600Glu S45
14 BAA02g34880 A02 30007882 G A intron_variant MODIFIER c.3248+44G>A| S136
15 BAA02g34880 A02 30007889 C T intron_variant MODIFIER c.3248+51C>T| S15
16 BAA02g34880 A02 30008080 C T intron_variant MODIFIER c.3249-93C>T| S239
17 BAA02g34880 A02 30008127 G A intron_variant MODIFIER c.3249-46G>A| S5
18 BAA02g34880 A02 30008634 C T intron_variant MODIFIER c.3515+195C>T| S92
19 BAA02g34880 A02 30008817 C T intron_variant MODIFIER c.3515+378C>T| S252
20 BAA02g34880 A02 30008818 G C intron_variant MODIFIER c.3515+379G>C| S257
21 BAA02g34880 A02 30009145 G A intron_variant MODIFIER c.3515+706G>A| S256
22 BAA02g34880 A02 30009364 G A intron_variant MODIFIER c.3515+925G>A| S19
23 BAA02g34880 A02 30010131 G A intron_variant MODIFIER c.3516-777G>A| S203
24 BAA02g34880 A02 30013500 G A intron_variant MODIFIER c.3861-619G>A| S56
25 BAA02g34880 A02 30017673 C T downstream_gene_variant MODIFIER c.*1069C>T| S177