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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g13600 A10 14592052 C T missense_variant MODERATE c.1117G>A|p.Gly373Arg S104
S52
2 BAA10g13600 A10 14592073 C T missense_variant MODERATE c.1096G>A|p.Ala366Thr S137
S45
3 BAA10g13600 A10 14592175 G A missense_variant MODERATE c.994C>T|p.Pro332Ser S217
S248
4 BAA10g13600 A10 14592479 G A synonymous_variant LOW c.690C>T|p.Ile230Ile S295
5 BAA10g13600 A10 14592611 G A missense_variant MODERATE c.632C>T|p.Ala211Val S236
6 BAA10g13600 A10 14592854 C T missense_variant MODERATE c.389G>A|p.Gly130Glu S230
S26
7 BAA10g13600 A10 14593126 G A synonymous_variant LOW c.117C>T|p.Thr39Thr S43
8 BAA10g13600 A10 14593235 G A missense_variant MODERATE c.8C>T|p.Ser3Phe S164
9 BAA10g13600 A10 14593799 G A upstream_gene_variant MODIFIER c.-557C>T| S127
10 BAA10g13600 A10 14594504 C T upstream_gene_variant MODIFIER c.-1262G>A| S116
11 BAA10g13600 A10 14594939 C T upstream_gene_variant MODIFIER c.-1697G>A| S116
12 BAA10g13600 A10 14596180 G A upstream_gene_variant MODIFIER c.-2938C>T| S175
13 BAA10g13600 A10 14597099 C T upstream_gene_variant MODIFIER c.-3857G>A| S122