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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g18060 A10 17085580 G A upstream_gene_variant MODIFIER c.-3031G>A| S35
2 BAA10g18060 A10 17086225 C T upstream_gene_variant MODIFIER c.-2386C>T| S10
3 BAA10g18060 A10 17086559 C T upstream_gene_variant MODIFIER c.-2052C>T| S68
4 BAA10g18060 A10 17086644 G A upstream_gene_variant MODIFIER c.-1967G>A| S3
5 BAA10g18060 A10 17086814 C T upstream_gene_variant MODIFIER c.-1797C>T| S256
6 BAA10g18060 A10 17087728 G A upstream_gene_variant MODIFIER c.-883G>A| S234
7 BAA10g18060 A10 17087824 C T upstream_gene_variant MODIFIER c.-787C>T| S201
8 BAA10g18060 A10 17089291 C T synonymous_variant LOW c.681C>T|p.Val227Val S201
9 BAA10g18060 A10 17089755 G A missense_variant MODERATE c.1145G>A|p.Arg382Lys S228
10 BAA10g18060 A10 17089823 G A missense_variant MODERATE c.1213G>A|p.Val405Met S98
11 BAA10g18060 A10 17089862 C T missense_variant MODERATE c.1252C>T|p.Leu418Phe S277
12 BAA10g18060 A10 17090023 C T synonymous_variant LOW c.1413C>T|p.Leu471Leu S199
13 BAA10g18060 A10 17090104 G A synonymous_variant LOW c.1494G>A|p.Arg498Arg S265
14 BAA10g18060 A10 17090189 G A missense_variant MODERATE c.1579G>A|p.Ala527Thr S59
15 BAA10g18060 A10 17090236 C T synonymous_variant LOW c.1626C>T|p.Tyr542Tyr S26
16 BAA10g18060 A10 17094131 G A downstream_gene_variant MODIFIER c.*3379G>A| S166
17 BAA10g18060 A10 17095359 C T downstream_gene_variant MODIFIER c.*4607C>T| S244
18 BAA10g18060 A10 17095366 G A downstream_gene_variant MODIFIER c.*4614G>A| S192
19 BAA10g18060 A10 17095664 G A downstream_gene_variant MODIFIER c.*4912G>A| S295