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 BAA10g19400 A10 17792424 C T upstream_gene_variant MODIFIER c.-3672C>T| S162
2 BAA10g19400 A10 17793014 G A upstream_gene_variant MODIFIER c.-3082G>A| S57
3 BAA10g19400 A10 17794173 C T upstream_gene_variant MODIFIER c.-1923C>T| S153
S213
4 BAA10g19400 A10 17794450 C T upstream_gene_variant MODIFIER c.-1646C>T| S189
5 BAA10g19400 A10 17794718 A G upstream_gene_variant MODIFIER c.-1378A>G| S189
6 BAA10g19400 A10 17795653 C T upstream_gene_variant MODIFIER c.-443C>T| S249
7 BAA10g19400 A10 17795676 G A upstream_gene_variant MODIFIER c.-420G>A| S174
8 BAA10g19400 A10 17798400 G A missense_variant MODERATE c.961G>A|p.Gly321Arg S36
9 BAA10g19400 A10 17799453 C T missense_variant MODERATE c.1309C>T|p.Pro437Ser S282
10 BAA10g19400 A10 17800656 G A missense_variant MODERATE c.2147G>A|p.Gly716Glu S131
11 BAA10g19400 A10 17800677 C T missense_variant MODERATE c.2168C>T|p.Thr723Ile S146
12 BAA10g19400 A10 17803375 C T downstream_gene_variant MODIFIER c.*1727C>T| S86
13 BAA10g19400 A10 17803456 C T downstream_gene_variant MODIFIER c.*1808C>T| S33
14 BAA10g19400 A10 17804396 C T downstream_gene_variant MODIFIER c.*2748C>T| S232
15 BAA10g19400 A10 17805634 C T downstream_gene_variant MODIFIER c.*3986C>T| S2