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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g00130 A10 45049 G A upstream_gene_variant MODIFIER c.-4933G>A| S251
2 BAA10g00130 A10 45372 C T upstream_gene_variant MODIFIER c.-4610C>T| S281
3 BAA10g00130 A10 46339 C T upstream_gene_variant MODIFIER c.-3643C>T| S12
4 BAA10g00130 A10 52147 G A stop_gained HIGH c.1497G>A|p.Trp499* S234
5 BAA10g00130 A10 52566 C T splice_region_variant&intron_variant LOW c.1708-3C>T| S286
6 BAA10g00130 A10 52595 G A synonymous_variant LOW c.1734G>A|p.Val578Val S67
7 BAA10g00130 A10 52700 G A intron_variant MODIFIER c.1830+9G>A| S57
8 BAA10g00130 A10 54058 C T intron_variant MODIFIER c.2506-135C>T| S56
9 BAA10g00130 A10 54307 G A missense_variant MODERATE c.2620G>A|p.Val874Ile S107
10 BAA10g00130 A10 55713 G A synonymous_variant LOW c.3393G>A|p.Lys1131Lys S60
11 BAA10g00130 A10 55901 G A missense_variant MODERATE c.3478G>A|p.Glu1160Lys S192
12 BAA10g00130 A10 56030 G A missense_variant MODERATE c.3607G>A|p.Asp1203Asn S215
13 BAA10g00130 A10 56956 G A missense_variant MODERATE c.4018G>A|p.Ala1340Thr S290
14 BAA10g00130 A10 57914 C T synonymous_variant LOW c.4599C>T|p.Ile1533Ile S202
15 BAA10g00130 A10 58471 G A missense_variant MODERATE c.4885G>A|p.Val1629Met S76
16 BAA10g00130 A10 58602 G A intron_variant MODIFIER c.4917+99G>A| S256
17 BAA10g00130 A10 58783 C T stop_gained HIGH c.4990C>T|p.Gln1664* S104
S52
18 BAA10g00130 A10 59078 C T intron_variant MODIFIER c.5113-45C>T| S87
19 BAA10g00130 A10 60469 G A missense_variant&splice_region_variant MODERATE c.5710G>A|p.Glu1904Lys S184
20 BAA10g00130 A10 60755 G A splice_region_variant&intron_variant LOW c.5889+5G>A| S153
S213