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 BAA09g51660 A09 53879727 C T missense_variant MODERATE c.4334G>A|p.Arg1445Lys S13
2 BAA09g51660 A09 53880126 C T stop_gained HIGH c.3935G>A|p.Trp1312* S256
3 BAA09g51660 A09 53881013 C T missense_variant MODERATE c.3202G>A|p.Gly1068Arg S232
4 BAA09g51660 A09 53881442 G A missense_variant MODERATE c.2915C>T|p.Pro972Leu S2
5 BAA09g51660 A09 53882788 G A missense_variant MODERATE c.1951C>T|p.Pro651Ser S74
6 BAA09g51660 A09 53883241 C T missense_variant MODERATE c.1498G>A|p.Gly500Arg S299
7 BAA09g51660 A09 53883243 G A missense_variant MODERATE c.1496C>T|p.Ser499Phe S81
S85
8 BAA09g51660 A09 53883551 C T synonymous_variant LOW c.1188G>A|p.Glu396Glu S104
S52
9 BAA09g51660 A09 53883690 C T missense_variant MODERATE c.1049G>A|p.Gly350Glu S57
10 BAA09g51660 A09 53883853 C T missense_variant MODERATE c.886G>A|p.Ala296Thr S232
11 BAA09g51660 A09 53884010 C T intron_variant MODIFIER c.749-20G>A| S293
12 BAA09g51660 A09 53884106 C T intron_variant MODIFIER c.748+91G>A| S169
13 BAA09g51660 A09 53884566 C T synonymous_variant LOW c.486G>A|p.Arg162Arg S302
14 BAA09g51660 A09 53885173 G A upstream_gene_variant MODIFIER c.-38C>T| S241
15 BAA09g51660 A09 53886157 C T upstream_gene_variant MODIFIER c.-1022G>A| S19
16 BAA09g51660 A09 53886886 C T upstream_gene_variant MODIFIER c.-1751G>A| S302
17 BAA09g51660 A09 53887104 C T upstream_gene_variant MODIFIER c.-1969G>A| S138
18 BAA09g51660 A09 53889588 C T upstream_gene_variant MODIFIER c.-4453G>A| S232