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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g04600 A05 2205539 C T upstream_gene_variant MODIFIER c.-4166C>T| S57
2 BAA05g04600 A05 2207083 C G upstream_gene_variant MODIFIER c.-2622C>G| S30
S31
3 BAA05g04600 A05 2208172 C T upstream_gene_variant MODIFIER c.-1533C>T| S92
4 BAA05g04600 A05 2208771 C T upstream_gene_variant MODIFIER c.-934C>T| S175
5 BAA05g04600 A05 2209274 G A upstream_gene_variant MODIFIER c.-431G>A| S122
6 BAA05g04600 A05 2209484 G A upstream_gene_variant MODIFIER c.-221G>A| S112
7 BAA05g04600 A05 2209636 C T upstream_gene_variant MODIFIER c.-69C>T| S163
8 BAA05g04600 A05 2211271 C T intron_variant MODIFIER c.442+537C>T| S61
9 BAA05g04600 A05 2211423 G A intron_variant MODIFIER c.442+689G>A| S273
10 BAA05g04600 A05 2211544 G A intron_variant MODIFIER c.442+810G>A| S48
11 BAA05g04600 A05 2211569 C T intron_variant MODIFIER c.442+835C>T| S36
12 BAA05g04600 A05 2213156 G A intron_variant MODIFIER c.442+2422G>A| S138
13 BAA05g04600 A05 2214724 C T intron_variant MODIFIER c.443-1117C>T| S53
14 BAA05g04600 A05 2215322 T A intron_variant MODIFIER c.443-519T>A| S162
15 BAA05g04600 A05 2215461 G A intron_variant MODIFIER c.443-380G>A| S192
16 BAA05g04600 A05 2216709 C T missense_variant MODERATE c.983C>T|p.Thr328Ile S41
17 BAA05g04600 A05 2216717 C T stop_gained HIGH c.991C>T|p.Gln331* S60
18 BAA05g04600 A05 2217099 C T missense_variant MODERATE c.1168C>T|p.Leu390Phe S207
19 BAA05g04600 A05 2217624 G A missense_variant MODERATE c.1459G>A|p.Asp487Asn S1
S90