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 BAA01g25160 A01 13502202 C T missense_variant MODERATE c.1103G>A|p.Gly368Glu S261
2 BAA01g25160 A01 13502237 G A synonymous_variant LOW c.1068C>T|p.Phe356Phe S239
3 BAA01g25160 A01 13502402 G A splice_region_variant&intron_variant LOW c.1014+8C>T| S84
S93
4 BAA01g25160 A01 13502409 C T splice_donor_variant&intron_variant HIGH c.1014+1G>A| S255
5 BAA01g25160 A01 13502514 G A intron_variant MODIFIER c.919-9C>T| S232
6 BAA01g25160 A01 13503245 G A missense_variant MODERATE c.509C>T|p.Ser170Phe S279
7 BAA01g25160 A01 13503778 G A missense_variant MODERATE c.320C>T|p.Ser107Phe S23
8 BAA01g25160 A01 13504091 C T intron_variant MODIFIER c.129+41G>A| S4
9 BAA01g25160 A01 13504183 G A synonymous_variant LOW c.78C>T|p.Leu26Leu S80
10 BAA01g25160 A01 13505151 C T upstream_gene_variant MODIFIER c.-891G>A| S200
11 BAA01g25160 A01 13506688 A G upstream_gene_variant MODIFIER c.-2428T>C| S210
12 BAA01g25160 A01 13508199 G A upstream_gene_variant MODIFIER c.-3939C>T| S142
S251
13 BAA01g25160 A01 13508218 G A upstream_gene_variant MODIFIER c.-3958C>T| S301
S304