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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g14900 A03 6177639 C T upstream_gene_variant MODIFIER c.-3754C>T| S44
2 BAA03g14900 A03 6177708 G A upstream_gene_variant MODIFIER c.-3685G>A| S128
3 BAA03g14900 A03 6178285 G A upstream_gene_variant MODIFIER c.-3108G>A| S229
4 BAA03g14900 A03 6178354 G A upstream_gene_variant MODIFIER c.-3039G>A| S213
5 BAA03g14900 A03 6178593 C T upstream_gene_variant MODIFIER c.-2800C>T| S217
6 BAA03g14900 A03 6179058 G A upstream_gene_variant MODIFIER c.-2335G>A| S159
S243
7 BAA03g14900 A03 6179303 C T upstream_gene_variant MODIFIER c.-2090C>T| S35
8 BAA03g14900 A03 6179395 G A upstream_gene_variant MODIFIER c.-1998G>A| S84
S93
9 BAA03g14900 A03 6180072 G A upstream_gene_variant MODIFIER c.-1321G>A| S25
S264
10 BAA03g14900 A03 6180255 G A upstream_gene_variant MODIFIER c.-1138G>A| S233
11 BAA03g14900 A03 6181469 G A missense_variant MODERATE c.77G>A|p.Cys26Tyr S94
12 BAA03g14900 A03 6181688 G A missense_variant MODERATE c.296G>A|p.Arg99His S267
13 BAA03g14900 A03 6185606 G A missense_variant MODERATE c.733G>A|p.Gly245Ser S206
S26
14 BAA03g14900 A03 6185837 C T stop_gained HIGH c.964C>T|p.Gln322* S82
S92