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 BAA08g33930 A08 22001174 C T synonymous_variant LOW c.2580G>A|p.Ala860Ala S295
2 BAA08g33930 A08 22001233 G A missense_variant MODERATE c.2521C>T|p.Pro841Ser S218
3 BAA08g33930 A08 22001303 C T stop_gained HIGH c.2451G>A|p.Trp817* S20
4 BAA08g33930 A08 22001732 G A synonymous_variant LOW c.2022C>T|p.Tyr674Tyr S139
5 BAA08g33930 A08 22001861 G A synonymous_variant LOW c.1893C>T|p.Ile631Ile S139
6 BAA08g33930 A08 22002169 G A synonymous_variant LOW c.1585C>T|p.Leu529Leu S119
7 BAA08g33930 A08 22002524 G A synonymous_variant LOW c.1230C>T|p.Val410Val S86
8 BAA08g33930 A08 22003295 G A synonymous_variant LOW c.459C>T|p.Phe153Phe S151
S263
9 BAA08g33930 A08 22003490 C T synonymous_variant LOW c.264G>A|p.Gln88Gln S282
10 BAA08g33930 A08 22003995 G A upstream_gene_variant MODIFIER c.-242C>T| S292
11 BAA08g33930 A08 22004450 G A upstream_gene_variant MODIFIER c.-697C>T| S40
S49
12 BAA08g33930 A08 22004532 A T upstream_gene_variant MODIFIER c.-779T>A| S170
13 BAA08g33930 A08 22005642 C T upstream_gene_variant MODIFIER c.-1889G>A| S262
14 BAA08g33930 A08 22005814 C T upstream_gene_variant MODIFIER c.-2061G>A| S286