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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g60800 A03 30650086 G A missense_variant MODERATE c.2351C>T|p.Pro784Leu S135
2 BAA03g60800 A03 30650255 G A missense_variant MODERATE c.2182C>T|p.Pro728Ser S262
3 BAA03g60800 A03 30650316 T C synonymous_variant LOW c.2121A>G|p.Pro707Pro S36
4 BAA03g60800 A03 30650349 G A synonymous_variant LOW c.2088C>T|p.Ser696Ser S121
5 BAA03g60800 A03 30650601 G A synonymous_variant LOW c.1836C>T|p.Ser612Ser S282
6 BAA03g60800 A03 30651247 C T missense_variant MODERATE c.1190G>A|p.Gly397Asp S187
7 BAA03g60800 A03 30651421 G A missense_variant MODERATE c.1016C>T|p.Ser339Phe S6
8 BAA03g60800 A03 30651465 C T synonymous_variant LOW c.972G>A|p.Ala324Ala S293
9 BAA03g60800 A03 30651653 T G missense_variant MODERATE c.784A>C|p.Asn262His S127
10 BAA03g60800 A03 30651765 G A synonymous_variant LOW c.672C>T|p.Phe224Phe S88
11 BAA03g60800 A03 30651820 G A missense_variant MODERATE c.617C>T|p.Pro206Leu S249
12 BAA03g60800 A03 30652085 C T missense_variant MODERATE c.352G>A|p.Val118Ile S91
13 BAA03g60800 A03 30652131 G A synonymous_variant LOW c.306C>T|p.Tyr102Tyr S69
14 BAA03g60800 A03 30652620 G A upstream_gene_variant MODIFIER c.-184C>T| S13
S64
15 BAA03g60800 A03 30653712 C T upstream_gene_variant MODIFIER c.-1276G>A| S201