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 BAA06g24390 A06 16248391 G A upstream_gene_variant MODIFIER c.-4587G>A| S185
2 BAA06g24390 A06 16248843 C T upstream_gene_variant MODIFIER c.-4135C>T| S108
3 BAA06g24390 A06 16250245 G A upstream_gene_variant MODIFIER c.-2733G>A| S264
4 BAA06g24390 A06 16251064 G A upstream_gene_variant MODIFIER c.-1914G>A| S69
5 BAA06g24390 A06 16251560 C T upstream_gene_variant MODIFIER c.-1418C>T| S84
S93
6 BAA06g24390 A06 16251637 G A upstream_gene_variant MODIFIER c.-1341G>A| S117
7 BAA06g24390 A06 16251671 G A upstream_gene_variant MODIFIER c.-1307G>A| S121
8 BAA06g24390 A06 16253831 C T missense_variant MODERATE c.533C>T|p.Thr178Ile S171
9 BAA06g24390 A06 16255247 C T synonymous_variant LOW c.1374C>T|p.Cys458Cys S218
10 BAA06g24390 A06 16255909 G A missense_variant MODERATE c.1861G>A|p.Ala621Thr S78
11 BAA06g24390 A06 16255969 G A missense_variant MODERATE c.1921G>A|p.Glu641Lys S160
12 BAA06g24390 A06 16256306 C T synonymous_variant LOW c.2173C>T|p.Leu725Leu S128
13 BAA06g24390 A06 16257602 G A missense_variant MODERATE c.3173G>A|p.Arg1058Lys S12
14 BAA06g24390 A06 16257606 C T synonymous_variant LOW c.3177C>T|p.Phe1059Phe S6
15 BAA06g24390 A06 16257771 C T synonymous_variant LOW c.3342C>T|p.Asp1114Asp S139
16 BAA06g24390 A06 16258581 G A missense_variant MODERATE c.3988G>A|p.Ala1330Thr S133
17 BAA06g24390 A06 16259185 C T missense_variant MODERATE c.4372C>T|p.Pro1458Ser S267
18 BAA06g24390 A06 16261641 G A downstream_gene_variant MODIFIER c.*2256G>A| S173
19 BAA06g24390 A06 16261660 G A downstream_gene_variant MODIFIER c.*2275G>A| S123
20 BAA06g24390 A06 16261748 G A downstream_gene_variant MODIFIER c.*2363G>A| S8
21 BAA06g24390 A06 16262624 G A downstream_gene_variant MODIFIER c.*3239G>A| S261
22 BAA06g24390 A06 16264131 G A downstream_gene_variant MODIFIER c.*4746G>A| S231
23 BAA06g24390 A06 16264264 C T downstream_gene_variant MODIFIER c.*4879C>T| S58