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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g66720 A09 60840547 G A synonymous_variant LOW c.2094C>T|p.Phe698Phe S47
2 BAA09g66720 A09 60840824 C T missense_variant MODERATE c.1817G>A|p.Gly606Glu S104
3 BAA09g66720 A09 60841200 C T missense_variant MODERATE c.1441G>A|p.Gly481Arg S293
4 BAA09g66720 A09 60841221 G A missense_variant MODERATE c.1420C>T|p.Leu474Phe S277
5 BAA09g66720 A09 60842320 C T missense_variant MODERATE c.811G>A|p.Asp271Asn S257
6 BAA09g66720 A09 60842690 G A splice_region_variant&synonymous_variant LOW c.654C>T|p.His218His S173
7 BAA09g66720 A09 60843575 G A missense_variant MODERATE c.239C>T|p.Ala80Val S205
8 BAA09g66720 A09 60843704 C T missense_variant MODERATE c.110G>A|p.Gly37Glu S168
9 BAA09g66720 A09 60844052 C T upstream_gene_variant MODIFIER c.-239G>A| S66
10 BAA09g66720 A09 60844277 C T upstream_gene_variant MODIFIER c.-464G>A| S289
S290
11 BAA09g66720 A09 60844615 C T upstream_gene_variant MODIFIER c.-802G>A| S82
S92
12 BAA09g66720 A09 60845767 G A upstream_gene_variant MODIFIER c.-1954C>T| S291
13 BAA09g66720 A09 60847262 C T upstream_gene_variant MODIFIER c.-3449G>A| S153
S213
14 BAA09g66720 A09 60848247 C T upstream_gene_variant MODIFIER c.-4434G>A| S267