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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g18310 A07 24344426 C T upstream_gene_variant MODIFIER c.-3008C>T| S162
2 BAA07g18310 A07 24344932 C T upstream_gene_variant MODIFIER c.-2502C>T| S203
3 BAA07g18310 A07 24345384 C T upstream_gene_variant MODIFIER c.-2050C>T| S155
4 BAA07g18310 A07 24345396 C T upstream_gene_variant MODIFIER c.-2038C>T| S164
5 BAA07g18310 A07 24345660 C T upstream_gene_variant MODIFIER c.-1774C>T| S69
6 BAA07g18310 A07 24345728 G T upstream_gene_variant MODIFIER c.-1706G>T| S245
7 BAA07g18310 A07 24347388 G A upstream_gene_variant MODIFIER c.-46G>A| S163
8 BAA07g18310 A07 24347737 G A missense_variant MODERATE c.304G>A|p.Asp102Asn S33
9 BAA07g18310 A07 24348043 G A missense_variant MODERATE c.610G>A|p.Gly204Ser S199
10 BAA07g18310 A07 24348303 G A synonymous_variant LOW c.870G>A|p.Ala290Ala S156
11 BAA07g18310 A07 24348304 T A missense_variant MODERATE c.871T>A|p.Phe291Ile S156
12 BAA07g18310 A07 24348364 G A missense_variant MODERATE c.931G>A|p.Val311Met S158
13 BAA07g18310 A07 24348368 G A missense_variant MODERATE c.935G>A|p.Arg312Lys S92
14 BAA07g18310 A07 24348475 C T stop_gained HIGH c.1042C>T|p.Gln348* S52
15 BAA07g18310 A07 24348693 C T missense_variant MODERATE c.1189C>T|p.Pro397Ser S198
16 BAA07g18310 A07 24348790 G A missense_variant MODERATE c.1286G>A|p.Gly429Asp S298
17 BAA07g18310 A07 24349422 G A missense_variant MODERATE c.1918G>A|p.Val640Met S225
18 BAA07g18310 A07 24350556 C T downstream_gene_variant MODIFIER c.*747C>T| S173
19 BAA07g18310 A07 24351549 C T downstream_gene_variant MODIFIER c.*1740C>T| S305
20 BAA07g18310 A07 24352482 C T downstream_gene_variant MODIFIER c.*2673C>T| S168
21 BAA07g18310 A07 24353269 C T downstream_gene_variant MODIFIER c.*3460C>T| S162
22 BAA07g18310 A07 24353763 C T downstream_gene_variant MODIFIER c.*3954C>T| S9
23 BAA07g18310 A07 24353832 G A downstream_gene_variant MODIFIER c.*4023G>A| S40
S49