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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g04570 A10 2329330 C T synonymous_variant LOW c.831G>A|p.Ser277Ser S40
S49
2 BAA10g04570 A10 2330736 C T missense_variant MODERATE c.116G>A|p.Gly39Glu S132
S137
S215
3 BAA10g04570 A10 2330787 G A missense_variant MODERATE c.65C>T|p.Thr22Ile S65
4 BAA10g04570 A10 2330937 G A upstream_gene_variant MODIFIER c.-86C>T| S257
5 BAA10g04570 A10 2331355 C T upstream_gene_variant MODIFIER c.-504G>A| S275
6 BAA10g04570 A10 2331643 C T upstream_gene_variant MODIFIER c.-792G>A| S132
S137
S215
S89
7 BAA10g04570 A10 2331650 C T upstream_gene_variant MODIFIER c.-799G>A| S256
8 BAA10g04570 A10 2332854 C T upstream_gene_variant MODIFIER c.-2003G>A| S88
9 BAA10g04570 A10 2335222 G A upstream_gene_variant MODIFIER c.-4371C>T| S172
S217
10 BAA10g04570 A10 2335244 G A upstream_gene_variant MODIFIER c.-4393C>T| S39
11 BAA10g04570 A10 2335351 G A upstream_gene_variant MODIFIER c.-4500C>T| S245
12 BAA10g04570 A10 2335488 G A upstream_gene_variant MODIFIER c.-4637C>T| S100
13 BAA10g04570 A10 2335804 G A upstream_gene_variant MODIFIER c.-4953C>T| S189