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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g39970 A09 47306970 C T upstream_gene_variant MODIFIER c.-2430C>T| S280
2 BAA09g39970 A09 47307282 C T upstream_gene_variant MODIFIER c.-2118C>T| S278
3 BAA09g39970 A09 47307290 C T upstream_gene_variant MODIFIER c.-2110C>T| S56
4 BAA09g39970 A09 47307751 C T upstream_gene_variant MODIFIER c.-1649C>T| S43
5 BAA09g39970 A09 47309069 C T upstream_gene_variant MODIFIER c.-331C>T| S235
6 BAA09g39970 A09 47309616 C T missense_variant MODERATE c.217C>T|p.Pro73Ser S242
7 BAA09g39970 A09 47310498 G A missense_variant MODERATE c.1099G>A|p.Glu367Lys S48
8 BAA09g39970 A09 47311221 G A missense_variant MODERATE c.1490G>A|p.Arg497Gln S226
9 BAA09g39970 A09 47311380 G A missense_variant MODERATE c.1649G>A|p.Gly550Glu S89
10 BAA09g39970 A09 47311641 C T missense_variant MODERATE c.1910C>T|p.Ser637Phe S286
11 BAA09g39970 A09 47311795 C T synonymous_variant LOW c.2064C>T|p.Leu688Leu S186
S229
12 BAA09g39970 A09 47311832 G A missense_variant MODERATE c.2101G>A|p.Asp701Asn S45
13 BAA09g39970 A09 47312049 G A missense_variant MODERATE c.2252G>A|p.Gly751Asp S20
14 BAA09g39970 A09 47312343 C T missense_variant MODERATE c.2546C>T|p.Pro849Leu S159
S243
S299
15 BAA09g39970 A09 47312868 C T intron_variant MODIFIER c.2607+464C>T| S121
16 BAA09g39970 A09 47312987 C T intron_variant MODIFIER c.2607+583C>T| S210
17 BAA09g39970 A09 47314133 G A downstream_gene_variant MODIFIER c.*52G>A| S247
18 BAA09g39970 A09 47314582 C T downstream_gene_variant MODIFIER c.*501C>T| S103
19 BAA09g39970 A09 47314839 G A downstream_gene_variant MODIFIER c.*758G>A| S35
20 BAA09g39970 A09 47315378 G A downstream_gene_variant MODIFIER c.*1297G>A| S217
S248
21 BAA09g39970 A09 47315774 G A downstream_gene_variant MODIFIER c.*1693G>A| S274
22 BAA09g39970 A09 47316077 G A downstream_gene_variant MODIFIER c.*1996G>A| S16
23 BAA09g39970 A09 47318142 C T downstream_gene_variant MODIFIER c.*4061C>T| S301
S304
24 BAA09g39970 A09 47318200 C T downstream_gene_variant MODIFIER c.*4119C>T| S183
S198