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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g04300 A02 1878518 G A missense_variant MODERATE c.2791C>T|p.Leu931Phe S105
S106
2 BAA02g04300 A02 1878691 G A splice_region_variant&intron_variant LOW c.2623-5C>T| S41
3 BAA02g04300 A02 1878843 G A synonymous_variant LOW c.2556C>T|p.Asn852Asn S125
4 BAA02g04300 A02 1879134 C T missense_variant MODERATE c.2356G>A|p.Val786Ile S76
5 BAA02g04300 A02 1879419 G A synonymous_variant LOW c.2268C>T|p.Gly756Gly S225
S73
6 BAA02g04300 A02 1879729 C A stop_gained HIGH c.2029G>T|p.Glu677* S203
7 BAA02g04300 A02 1879903 C T missense_variant MODERATE c.1855G>A|p.Glu619Lys S179
8 BAA02g04300 A02 1880002 C T missense_variant MODERATE c.1756G>A|p.Val586Met S89
9 BAA02g04300 A02 1880066 C T synonymous_variant LOW c.1692G>A|p.Val564Val S183
S198
10 BAA02g04300 A02 1880551 C T missense_variant MODERATE c.1207G>A|p.Gly403Arg S179
11 BAA02g04300 A02 1880839 C T missense_variant MODERATE c.919G>A|p.Glu307Lys S133
12 BAA02g04300 A02 1881348 C T synonymous_variant LOW c.498G>A|p.Glu166Glu S39
13 BAA02g04300 A02 1881612 G A stop_gained HIGH c.352C>T|p.Gln118* S209
14 BAA02g04300 A02 1881632 G A missense_variant MODERATE c.332C>T|p.Ala111Val S168
15 BAA02g04300 A02 1882161 C T synonymous_variant LOW c.165G>A|p.Lys55Lys S150
16 BAA02g04300 A02 1885932 C T upstream_gene_variant MODIFIER c.-3342G>A| S250
17 BAA02g04300 A02 1886329 C T upstream_gene_variant MODIFIER c.-3739G>A| S284
18 BAA02g04300 A02 1886565 C T upstream_gene_variant MODIFIER c.-3975G>A| S257