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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g05770 A08 4439799 G A downstream_gene_variant MODIFIER c.*3764C>T| S32
2 BAA08g05770 A08 4440337 C T downstream_gene_variant MODIFIER c.*3226G>A| S82
S92
3 BAA08g05770 A08 4441641 G A downstream_gene_variant MODIFIER c.*1922C>T| S262
4 BAA08g05770 A08 4443760 C T missense_variant MODERATE c.1915G>A|p.Glu639Lys S174
S216
S241
5 BAA08g05770 A08 4443800 G A synonymous_variant LOW c.1875C>T|p.Tyr625Tyr S240
6 BAA08g05770 A08 4443868 C T missense_variant MODERATE c.1807G>A|p.Glu603Lys S132
S137
S89
7 BAA08g05770 A08 4443870 G A missense_variant MODERATE c.1805C>T|p.Ser602Leu S242
8 BAA08g05770 A08 4444139 G A synonymous_variant LOW c.1536C>T|p.Tyr512Tyr S249
9 BAA08g05770 A08 4444379 C T synonymous_variant LOW c.1365G>A|p.Ser455Ser S143
10 BAA08g05770 A08 4444555 G A missense_variant MODERATE c.1256C>T|p.Pro419Leu S169
11 BAA08g05770 A08 4444708 C T missense_variant MODERATE c.1103G>A|p.Gly368Asp S173
12 BAA08g05770 A08 4444849 G A missense_variant MODERATE c.962C>T|p.Pro321Leu S246
13 BAA08g05770 A08 4445162 G A missense_variant MODERATE c.833C>T|p.Thr278Ile S58
14 BAA08g05770 A08 4445543 C T stop_gained HIGH c.452G>A|p.Trp151* S28
15 BAA08g05770 A08 4447206 G A upstream_gene_variant MODIFIER c.-981C>T| S286
16 BAA08g05770 A08 4447237 G A upstream_gene_variant MODIFIER c.-1012C>T| S107
17 BAA08g05770 A08 4447362 G A upstream_gene_variant MODIFIER c.-1137C>T| S19
18 BAA08g05770 A08 4447472 C T upstream_gene_variant MODIFIER c.-1247G>A| S184
19 BAA08g05770 A08 4447556 G A upstream_gene_variant MODIFIER c.-1331C>T| S85
20 BAA08g05770 A08 4447799 C T upstream_gene_variant MODIFIER c.-1574G>A| S231
21 BAA08g05770 A08 4448749 C T upstream_gene_variant MODIFIER c.-2524G>A| S78
S83
22 BAA08g05770 A08 4450862 C T upstream_gene_variant MODIFIER c.-4637G>A| S164