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 BAA07g03590 A07 2920727 G A upstream_gene_variant MODIFIER c.-4832G>A| S54
2 BAA07g03590 A07 2920944 G A upstream_gene_variant MODIFIER c.-4615G>A| S19
3 BAA07g03590 A07 2921194 C T upstream_gene_variant MODIFIER c.-4365C>T| S249
S82
S92
4 BAA07g03590 A07 2921198 C T upstream_gene_variant MODIFIER c.-4361C>T| S259
5 BAA07g03590 A07 2921501 C T upstream_gene_variant MODIFIER c.-4058C>T| S297
6 BAA07g03590 A07 2922313 G A upstream_gene_variant MODIFIER c.-3246G>A| S78
7 BAA07g03590 A07 2922457 G A upstream_gene_variant MODIFIER c.-3102G>A| S19
8 BAA07g03590 A07 2923135 C T upstream_gene_variant MODIFIER c.-2424C>T| S213
9 BAA07g03590 A07 2923382 C T upstream_gene_variant MODIFIER c.-2177C>T| S142
10 BAA07g03590 A07 2923468 G A upstream_gene_variant MODIFIER c.-2091G>A| S46
11 BAA07g03590 A07 2923799 T G upstream_gene_variant MODIFIER c.-1760T>G| S206
12 BAA07g03590 A07 2923935 C T upstream_gene_variant MODIFIER c.-1624C>T| S267
13 BAA07g03590 A07 2924534 C T upstream_gene_variant MODIFIER c.-1025C>T| S280
14 BAA07g03590 A07 2926044 C T synonymous_variant LOW c.417C>T|p.Phe139Phe S276
15 BAA07g03590 A07 2926426 G A missense_variant MODERATE c.799G>A|p.Ala267Thr S245
16 BAA07g03590 A07 2926955 G A missense_variant MODERATE c.1043G>A|p.Gly348Asp S179
17 BAA07g03590 A07 2927032 C T missense_variant MODERATE c.1120C>T|p.Pro374Ser S35
18 BAA07g03590 A07 2927049 G A synonymous_variant LOW c.1137G>A|p.Leu379Leu S76
19 BAA07g03590 A07 2927110 C T stop_gained HIGH c.1198C>T|p.Gln400* S64
20 BAA07g03590 A07 2931430 G A downstream_gene_variant MODIFIER c.*3009G>A| S298
21 BAA07g03590 A07 2932450 G A downstream_gene_variant MODIFIER c.*4029G>A| S33
22 BAA07g03590 A07 2932507 G A downstream_gene_variant MODIFIER c.*4086G>A| S159
S243
S299
23 BAA07g03590 A07 2933249 G A downstream_gene_variant MODIFIER c.*4828G>A| S209