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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g36920 A09 45108031 C T upstream_gene_variant MODIFIER c.-4105C>T| S144
2 BAA09g36920 A09 45108448 C T upstream_gene_variant MODIFIER c.-3688C>T| S138
3 BAA09g36920 A09 45108725 G A upstream_gene_variant MODIFIER c.-3411G>A| S276
4 BAA09g36920 A09 45108776 G A upstream_gene_variant MODIFIER c.-3360G>A| S132
S137
S89
5 BAA09g36920 A09 45109206 C T upstream_gene_variant MODIFIER c.-2930C>T| S143
6 BAA09g36920 A09 45109374 C T upstream_gene_variant MODIFIER c.-2762C>T| S277
7 BAA09g36920 A09 45110259 C T upstream_gene_variant MODIFIER c.-1877C>T| S83
S88
8 BAA09g36920 A09 45110303 C T upstream_gene_variant MODIFIER c.-1833C>T| S32
9 BAA09g36920 A09 45111021 C T upstream_gene_variant MODIFIER c.-1115C>T| S135
10 BAA09g36920 A09 45112164 C T missense_variant MODERATE c.29C>T|p.Pro10Leu S100
11 BAA09g36920 A09 45112795 C T missense_variant MODERATE c.491C>T|p.Ser164Phe S5
12 BAA09g36920 A09 45113892 G A missense_variant MODERATE c.1240G>A|p.Glu414Lys S112
13 BAA09g36920 A09 45113954 G A splice_donor_variant&intron_variant HIGH c.1301+1G>A| S265
14 BAA09g36920 A09 45114036 C T missense_variant MODERATE c.1312C>T|p.Pro438Ser S188
15 BAA09g36920 A09 45114103 G A missense_variant MODERATE c.1379G>A|p.Gly460Asp S197
16 BAA09g36920 A09 45114267 G A splice_donor_variant&intron_variant HIGH c.1542+1G>A| S62
17 BAA09g36920 A09 45114445 C T synonymous_variant LOW c.1653C>T|p.Asn551Asn S50
18 BAA09g36920 A09 45115324 C T downstream_gene_variant MODIFIER c.*684C>T| S188