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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g02860 A08 2041265 G A upstream_gene_variant MODIFIER c.-4926G>A| S263
2 BAA08g02860 A08 2042184 C T upstream_gene_variant MODIFIER c.-4007C>T| S60
3 BAA08g02860 A08 2042615 G A upstream_gene_variant MODIFIER c.-3576G>A| S221
4 BAA08g02860 A08 2043417 C T upstream_gene_variant MODIFIER c.-2774C>T| S46
5 BAA08g02860 A08 2043434 G A upstream_gene_variant MODIFIER c.-2757G>A| S153
6 BAA08g02860 A08 2043531 G A upstream_gene_variant MODIFIER c.-2660G>A| S34
7 BAA08g02860 A08 2043876 C T upstream_gene_variant MODIFIER c.-2315C>T| S289
S290
8 BAA08g02860 A08 2044058 C T upstream_gene_variant MODIFIER c.-2133C>T| S122
9 BAA08g02860 A08 2044106 C T upstream_gene_variant MODIFIER c.-2085C>T| S86
10 BAA08g02860 A08 2044321 C T upstream_gene_variant MODIFIER c.-1870C>T| S2
11 BAA08g02860 A08 2044727 C T upstream_gene_variant MODIFIER c.-1464C>T| S162
12 BAA08g02860 A08 2046010 C T upstream_gene_variant MODIFIER c.-181C>T| S215
13 BAA08g02860 A08 2046215 G A missense_variant MODERATE c.25G>A|p.Asp9Asn S98
14 BAA08g02860 A08 2046325 C T synonymous_variant LOW c.135C>T|p.Val45Val S59
15 BAA08g02860 A08 2046333 G A missense_variant MODERATE c.143G>A|p.Gly48Glu S125
16 BAA08g02860 A08 2046489 C T missense_variant MODERATE c.299C>T|p.Ser100Phe S51
17 BAA08g02860 A08 2047437 G A missense_variant MODERATE c.667G>A|p.Glu223Lys S221
18 BAA08g02860 A08 2051941 T G downstream_gene_variant MODIFIER c.*3706T>G| S304
19 BAA08g02860 A08 2052116 C T downstream_gene_variant MODIFIER c.*3881C>T| S201
20 BAA08g02860 A08 2052380 C T downstream_gene_variant MODIFIER c.*4145C>T| S152