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


Gene ID

Results: 1 - 32 of 32 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g20610 A05 12775529 G A upstream_gene_variant MODIFIER c.-4449G>A| S41
2 BAA05g20610 A05 12776028 G A upstream_gene_variant MODIFIER c.-3950G>A| S1
S90
3 BAA05g20610 A05 12776354 G A upstream_gene_variant MODIFIER c.-3624G>A| S190
4 BAA05g20610 A05 12776543 G A upstream_gene_variant MODIFIER c.-3435G>A| S39
5 BAA05g20610 A05 12776744 G A upstream_gene_variant MODIFIER c.-3234G>A| S126
S133
6 BAA05g20610 A05 12778565 G A upstream_gene_variant MODIFIER c.-1413G>A| S288
7 BAA05g20610 A05 12778568 A C upstream_gene_variant MODIFIER c.-1410A>C| S217
8 BAA05g20610 A05 12778585 G A upstream_gene_variant MODIFIER c.-1393G>A| S249
9 BAA05g20610 A05 12778666 G A upstream_gene_variant MODIFIER c.-1312G>A| S188
10 BAA05g20610 A05 12779605 G A upstream_gene_variant MODIFIER c.-373G>A| S187
11 BAA05g20610 A05 12780030 G A missense_variant MODERATE c.53G>A|p.Gly18Asp S173
12 BAA05g20610 A05 12780090 G A missense_variant MODERATE c.113G>A|p.Gly38Glu S266
13 BAA05g20610 A05 12780230 C T stop_gained HIGH c.253C>T|p.Gln85* S207
14 BAA05g20610 A05 12780409 C T synonymous_variant LOW c.432C>T|p.His144His S142
15 BAA05g20610 A05 12780515 G A missense_variant MODERATE c.538G>A|p.Ala180Thr S157
16 BAA05g20610 A05 12781018 C T missense_variant MODERATE c.955C>T|p.Leu319Phe S268
17 BAA05g20610 A05 12781175 C T synonymous_variant LOW c.1038C>T|p.Phe346Phe S146
18 BAA05g20610 A05 12781400 G A missense_variant MODERATE c.1178G>A|p.Arg393Lys S294
19 BAA05g20610 A05 12782359 C T synonymous_variant LOW c.1779C>T|p.Ile593Ile S241
20 BAA05g20610 A05 12783192 C T synonymous_variant LOW c.2013C>T|p.Phe671Phe S268
21 BAA05g20610 A05 12783623 G A missense_variant MODERATE c.2278G>A|p.Glu760Lys S190
22 BAA05g20610 A05 12783987 C T synonymous_variant LOW c.2529C>T|p.Asp843Asp S59
23 BAA05g20610 A05 12784059 C T synonymous_variant LOW c.2601C>T|p.Leu867Leu S137
S215
24 BAA05g20610 A05 12784624 C T synonymous_variant LOW c.2883C>T|p.Arg961Arg S19
25 BAA05g20610 A05 12786769 G A downstream_gene_variant MODIFIER c.*1328G>A| S132
S137