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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g20330 A10 18330495 C T upstream_gene_variant MODIFIER c.-2358C>T| S244
2 BAA10g20330 A10 18330572 C T upstream_gene_variant MODIFIER c.-2281C>T| S221
3 BAA10g20330 A10 18331567 G A upstream_gene_variant MODIFIER c.-1286G>A| S160
4 BAA10g20330 A10 18333226 G A missense_variant MODERATE c.163G>A|p.Glu55Lys S42
5 BAA10g20330 A10 18333906 C T intron_variant MODIFIER c.582+33C>T| S122
6 BAA10g20330 A10 18334345 G A intron_variant MODIFIER c.656-28G>A| S9
7 BAA10g20330 A10 18335328 C T intron_variant MODIFIER c.999+238C>T| S157
S163
8 BAA10g20330 A10 18335920 G A synonymous_variant LOW c.1134G>A|p.Glu378Glu S33
9 BAA10g20330 A10 18336253 G A intron_variant MODIFIER c.1226+241G>A| S298
10 BAA10g20330 A10 18336655 G A stop_gained HIGH c.1326G>A|p.Trp442* S212
11 BAA10g20330 A10 18337707 G A synonymous_variant LOW c.1995G>A|p.Pro665Pro S46
12 BAA10g20330 A10 18339261 C T missense_variant MODERATE c.3062C>T|p.Ala1021Val S161
13 BAA10g20330 A10 18339385 C T synonymous_variant LOW c.3096C>T|p.Leu1032Leu S77
14 BAA10g20330 A10 18339404 G A missense_variant MODERATE c.3115G>A|p.Glu1039Lys S272
15 BAA10g20330 A10 18340012 C T missense_variant MODERATE c.3482C>T|p.Ala1161Val S26
16 BAA10g20330 A10 18341951 G A missense_variant MODERATE c.4864G>A|p.Ala1622Thr S18