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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g01480 A10 743448 G A upstream_gene_variant MODIFIER c.-3442G>A| S133
2 BAA10g01480 A10 744064 C T upstream_gene_variant MODIFIER c.-2826C>T| S206
S210
S26
3 BAA10g01480 A10 744244 C T upstream_gene_variant MODIFIER c.-2646C>T| S113
4 BAA10g01480 A10 744418 G A upstream_gene_variant MODIFIER c.-2472G>A| S264
5 BAA10g01480 A10 744776 C T upstream_gene_variant MODIFIER c.-2114C>T| S31
6 BAA10g01480 A10 745174 G A upstream_gene_variant MODIFIER c.-1716G>A| S69
7 BAA10g01480 A10 745507 G A upstream_gene_variant MODIFIER c.-1383G>A| S17
8 BAA10g01480 A10 745854 G A upstream_gene_variant MODIFIER c.-1036G>A| S48
9 BAA10g01480 A10 746009 C T upstream_gene_variant MODIFIER c.-881C>T| S221
10 BAA10g01480 A10 746450 C T upstream_gene_variant MODIFIER c.-440C>T| S31
11 BAA10g01480 A10 746577 G A upstream_gene_variant MODIFIER c.-313G>A| S211
S227
12 BAA10g01480 A10 747991 C T synonymous_variant LOW c.516C>T|p.Val172Val S31
13 BAA10g01480 A10 748418 G A missense_variant MODERATE c.757G>A|p.Asp253Asn S219
S72
14 BAA10g01480 A10 749462 C T synonymous_variant LOW c.1479C>T|p.Thr493Thr S286
15 BAA10g01480 A10 749540 C T synonymous_variant LOW c.1557C>T|p.Asn519Asn S113