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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g69190 A09 61857902 C T upstream_gene_variant MODIFIER c.-3215C>T| S77
S82
2 BAA09g69190 A09 61858209 C T upstream_gene_variant MODIFIER c.-2908C>T| S142
3 BAA09g69190 A09 61861085 C T upstream_gene_variant MODIFIER c.-32C>T| S176
4 BAA09g69190 A09 61861184 C T missense_variant MODERATE c.68C>T|p.Ser23Phe S183
S198
5 BAA09g69190 A09 61861409 G A missense_variant MODERATE c.293G>A|p.Gly98Glu S57
6 BAA09g69190 A09 61861846 C T intron_variant MODIFIER c.624+9C>T| S250
7 BAA09g69190 A09 61862562 C T intron_variant MODIFIER c.624+725C>T| S159
S299
8 BAA09g69190 A09 61862890 C T intron_variant MODIFIER c.624+1053C>T| S122
9 BAA09g69190 A09 61863111 G A intron_variant MODIFIER c.624+1274G>A| S79
S84
10 BAA09g69190 A09 61863457 G A intron_variant MODIFIER c.625-1449G>A| S98
11 BAA09g69190 A09 61863608 C T intron_variant MODIFIER c.625-1298C>T| S171
12 BAA09g69190 A09 61864514 C T intron_variant MODIFIER c.625-392C>T| S149
13 BAA09g69190 A09 61865312 C T intron_variant MODIFIER c.880+66C>T| S301
S304
14 BAA09g69190 A09 61865691 G A intron_variant MODIFIER c.880+445G>A| S1
S90
15 BAA09g69190 A09 61866888 G A missense_variant MODERATE c.959G>A|p.Gly320Glu S226
16 BAA09g69190 A09 61866993 C T intron_variant MODIFIER c.966-12C>T| S64
17 BAA09g69190 A09 61867510 C T missense_variant MODERATE c.1471C>T|p.Pro491Ser S164