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 BAA05g16730 A05 9305007 C T missense_variant MODERATE c.1565G>A|p.Gly522Glu S281
2 BAA05g16730 A05 9305017 C T missense_variant MODERATE c.1555G>A|p.Gly519Arg S246
3 BAA05g16730 A05 9305163 C T missense_variant MODERATE c.1409G>A|p.Gly470Glu S11
4 BAA05g16730 A05 9305235 C T missense_variant MODERATE c.1337G>A|p.Gly446Glu S108
5 BAA05g16730 A05 9305323 C T splice_region_variant&intron_variant LOW c.1255-6G>A| S19
6 BAA05g16730 A05 9305991 G A missense_variant MODERATE c.761C>T|p.Thr254Ile S138
7 BAA05g16730 A05 9306753 G A missense_variant MODERATE c.224C>T|p.Ser75Phe S148
8 BAA05g16730 A05 9307388 G A upstream_gene_variant MODIFIER c.-412C>T| S156
9 BAA05g16730 A05 9308860 C T upstream_gene_variant MODIFIER c.-1884G>A| S45
10 BAA05g16730 A05 9308912 C T upstream_gene_variant MODIFIER c.-1936G>A| S247
11 BAA05g16730 A05 9310432 G A upstream_gene_variant MODIFIER c.-3456C>T| S297
12 BAA05g16730 A05 9310902 G A upstream_gene_variant MODIFIER c.-3926C>T| S297
13 BAA05g16730 A05 9311201 C T upstream_gene_variant MODIFIER c.-4225G>A| S136