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


Gene ID

Results: 1 - 28 of 28 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g29350 A06 19994143 G A upstream_gene_variant MODIFIER c.-4893G>A| S263
2 BAA06g29350 A06 19994377 C T upstream_gene_variant MODIFIER c.-4659C>T| S150
3 BAA06g29350 A06 19994990 G A upstream_gene_variant MODIFIER c.-4046G>A| S39
4 BAA06g29350 A06 19995354 G A upstream_gene_variant MODIFIER c.-3682G>A| S194
5 BAA06g29350 A06 19995362 G A upstream_gene_variant MODIFIER c.-3674G>A| S143
6 BAA06g29350 A06 19995397 C T upstream_gene_variant MODIFIER c.-3639C>T| S246
7 BAA06g29350 A06 19995529 A T upstream_gene_variant MODIFIER c.-3507A>T| S262
8 BAA06g29350 A06 19996174 G A upstream_gene_variant MODIFIER c.-2862G>A| S33
9 BAA06g29350 A06 19997067 C T upstream_gene_variant MODIFIER c.-1969C>T| S42
10 BAA06g29350 A06 19997894 G A upstream_gene_variant MODIFIER c.-1142G>A| S50
11 BAA06g29350 A06 19999351 G A synonymous_variant LOW c.93G>A|p.Val31Val S33
12 BAA06g29350 A06 19999386 G A missense_variant MODERATE c.128G>A|p.Arg43Lys S261
13 BAA06g29350 A06 19999981 C T missense_variant MODERATE c.553C>T|p.His185Tyr S152
14 BAA06g29350 A06 20000018 C T splice_region_variant&intron_variant LOW c.586+4C>T| S189
15 BAA06g29350 A06 20000212 G A missense_variant MODERATE c.718G>A|p.Asp240Asn S35
16 BAA06g29350 A06 20000583 G A missense_variant MODERATE c.1007G>A|p.Arg336Lys S209
17 BAA06g29350 A06 20000607 C T intron_variant MODIFIER c.1019+12C>T| S62
18 BAA06g29350 A06 20000666 G A intron_variant MODIFIER c.1020-9G>A| S162
19 BAA06g29350 A06 20000790 G A missense_variant MODERATE c.1135G>A|p.Ala379Thr S13
20 BAA06g29350 A06 20002108 C T missense_variant MODERATE c.1876C>T|p.Pro626Ser S10
21 BAA06g29350 A06 20002890 C T intron_variant MODIFIER c.2317-60C>T| S259
22 BAA06g29350 A06 20003267 C T synonymous_variant LOW c.2634C>T|p.Ile878Ile S120
23 BAA06g29350 A06 20003820 C T missense_variant MODERATE c.3103C>T|p.Leu1035Phe S55
24 BAA06g29350 A06 20005723 C T downstream_gene_variant MODIFIER c.*1757C>T| S283
25 BAA06g29350 A06 20006033 G A downstream_gene_variant MODIFIER c.*2067G>A| S32