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 BAA10g12130 A10 13610955 C T upstream_gene_variant MODIFIER c.-4475C>T| S199
2 BAA10g12130 A10 13613695 C T upstream_gene_variant MODIFIER c.-1735C>T| S297
3 BAA10g12130 A10 13614331 C T upstream_gene_variant MODIFIER c.-1099C>T| S225
S73
4 BAA10g12130 A10 13614696 C T upstream_gene_variant MODIFIER c.-734C>T| S140
5 BAA10g12130 A10 13614748 G A upstream_gene_variant MODIFIER c.-682G>A| S155
6 BAA10g12130 A10 13614901 C T upstream_gene_variant MODIFIER c.-529C>T| S144
7 BAA10g12130 A10 13614934 G A upstream_gene_variant MODIFIER c.-496G>A| S13
8 BAA10g12130 A10 13615072 G A upstream_gene_variant MODIFIER c.-358G>A| S1
S90
9 BAA10g12130 A10 13615080 G A upstream_gene_variant MODIFIER c.-350G>A| S158
10 BAA10g12130 A10 13615570 C T synonymous_variant LOW c.141C>T|p.Ile47Ile S162
11 BAA10g12130 A10 13615596 C T missense_variant MODERATE c.167C>T|p.Ser56Phe S156
12 BAA10g12130 A10 13618263 G A missense_variant MODERATE c.869G>A|p.Gly290Glu S50
13 BAA10g12130 A10 13618681 G A downstream_gene_variant MODIFIER c.*192G>A| S280
14 BAA10g12130 A10 13619165 C T downstream_gene_variant MODIFIER c.*676C>T| S149