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 BAA09g68740 A09 61676667 G A upstream_gene_variant MODIFIER c.-4527G>A| S202
2 BAA09g68740 A09 61678488 C T upstream_gene_variant MODIFIER c.-2706C>T| S169
3 BAA09g68740 A09 61678585 G A upstream_gene_variant MODIFIER c.-2609G>A| S123
4 BAA09g68740 A09 61679074 G A upstream_gene_variant MODIFIER c.-2120G>A| S41
5 BAA09g68740 A09 61679379 G A upstream_gene_variant MODIFIER c.-1815G>A| S84
S93
6 BAA09g68740 A09 61679667 G A upstream_gene_variant MODIFIER c.-1527G>A| S184
7 BAA09g68740 A09 61681108 G A upstream_gene_variant MODIFIER c.-86G>A| S151
8 BAA09g68740 A09 61681114 C T upstream_gene_variant MODIFIER c.-80C>T| S175
9 BAA09g68740 A09 61682885 C T stop_gained HIGH c.685C>T|p.Arg229* S100
10 BAA09g68740 A09 61683266 G A intron_variant MODIFIER c.886-53G>A| S234
11 BAA09g68740 A09 61683627 G A intron_variant MODIFIER c.952-85G>A| S231
12 BAA09g68740 A09 61683963 G A intron_variant MODIFIER c.1067-22G>A| S266
13 BAA09g68740 A09 61686579 C T missense_variant MODERATE c.3251C>T|p.Pro1084Leu S11
14 BAA09g68740 A09 61687079 C T missense_variant MODERATE c.3751C>T|p.Leu1251Phe S42
15 BAA09g68740 A09 61687157 G A missense_variant MODERATE c.3829G>A|p.Asp1277Asn S167
16 BAA09g68740 A09 61687563 C T intron_variant MODIFIER c.4151-12C>T| S279
17 BAA09g68740 A09 61688149 C T synonymous_variant LOW c.4725C>T|p.Leu1575Leu S279
18 BAA09g68740 A09 61688474 G A missense_variant MODERATE c.5050G>A|p.Gly1684Arg S25
19 BAA09g68740 A09 61688549 C T missense_variant MODERATE c.5125C>T|p.Leu1709Phe S289
S290
20 BAA09g68740 A09 61688672 C T missense_variant MODERATE c.5248C>T|p.Pro1750Ser S301
S304
21 BAA09g68740 A09 61689944 C T missense_variant MODERATE c.6250C>T|p.Leu2084Phe S54
22 BAA09g68740 A09 61690590 C T missense_variant MODERATE c.6896C>T|p.Pro2299Leu S286
23 BAA09g68740 A09 61691181 G A missense_variant MODERATE c.7487G>A|p.Gly2496Asp S247
24 BAA09g68740 A09 61691764 C T synonymous_variant LOW c.8070C>T|p.Ser2690Ser S169
25 BAA09g68740 A09 61691800 C T synonymous_variant LOW c.8106C>T|p.Asp2702Asp S34