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 BAA09g58990 A09 57377826 C T missense_variant MODERATE c.1208G>A|p.Ser403Asn S75
S81
2 BAA09g58990 A09 57378491 G A synonymous_variant LOW c.543C>T|p.Ile181Ile S15
S3
3 BAA09g58990 A09 57379650 C T upstream_gene_variant MODIFIER c.-43G>A| S43
4 BAA09g58990 A09 57379903 G A upstream_gene_variant MODIFIER c.-296C>T| S13
5 BAA09g58990 A09 57380036 G A upstream_gene_variant MODIFIER c.-429C>T| S202
6 BAA09g58990 A09 57380427 G A upstream_gene_variant MODIFIER c.-820C>T| S65
7 BAA09g58990 A09 57381305 G A upstream_gene_variant MODIFIER c.-1698C>T| S241
8 BAA09g58990 A09 57381320 G A upstream_gene_variant MODIFIER c.-1713C>T| S240
9 BAA09g58990 A09 57381905 C T upstream_gene_variant MODIFIER c.-2298G>A| S159
10 BAA09g58990 A09 57382649 C T upstream_gene_variant MODIFIER c.-3042G>A| S251
11 BAA09g58990 A09 57382760 C T upstream_gene_variant MODIFIER c.-3153G>A| S13
12 BAA09g58990 A09 57382785 C T upstream_gene_variant MODIFIER c.-3178G>A| S186
13 BAA09g58990 A09 57383727 C T upstream_gene_variant MODIFIER c.-4120G>A| S63
14 BAA09g58990 A09 57384468 C T upstream_gene_variant MODIFIER c.-4861G>A| S146