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 BAA06g24190 A06 16074824 C T synonymous_variant LOW c.165G>A|p.Leu55Leu S42
2 BAA06g24190 A06 16075096 G A missense_variant MODERATE c.8C>T|p.Ser3Phe S219
S72
3 BAA06g24190 A06 16076050 C T upstream_gene_variant MODIFIER c.-947G>A| S159
S243
4 BAA06g24190 A06 16076214 C T upstream_gene_variant MODIFIER c.-1111G>A| S247
5 BAA06g24190 A06 16076629 A C upstream_gene_variant MODIFIER c.-1526T>G| S38
6 BAA06g24190 A06 16076832 G A upstream_gene_variant MODIFIER c.-1729C>T| S17
7 BAA06g24190 A06 16077503 C T upstream_gene_variant MODIFIER c.-2400G>A| S62
8 BAA06g24190 A06 16078350 G A upstream_gene_variant MODIFIER c.-3247C>T| S119
9 BAA06g24190 A06 16078488 G A upstream_gene_variant MODIFIER c.-3385C>T| S123
10 BAA06g24190 A06 16078619 C T upstream_gene_variant MODIFIER c.-3516G>A| S46
11 BAA06g24190 A06 16078681 C T upstream_gene_variant MODIFIER c.-3578G>A| S117
12 BAA06g24190 A06 16078683 C T upstream_gene_variant MODIFIER c.-3580G>A| S124
13 BAA06g24190 A06 16079744 C T upstream_gene_variant MODIFIER c.-4641G>A| S165
14 BAA06g24190 A06 16080019 G A upstream_gene_variant MODIFIER c.-4916C>T| S132
S137
S215
S89