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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g38670 A02 32920669 C T upstream_gene_variant MODIFIER c.-4013C>T| S271
2 BAA02g38670 A02 32920760 C T upstream_gene_variant MODIFIER c.-3922C>T| S94
3 BAA02g38670 A02 32921437 C T upstream_gene_variant MODIFIER c.-3245C>T| S301
S304
4 BAA02g38670 A02 32921560 C T upstream_gene_variant MODIFIER c.-3122C>T| S39
5 BAA02g38670 A02 32923054 C T upstream_gene_variant MODIFIER c.-1628C>T| S202
6 BAA02g38670 A02 32923076 C T upstream_gene_variant MODIFIER c.-1606C>T| S242
7 BAA02g38670 A02 32923521 C T upstream_gene_variant MODIFIER c.-1161C>T| S249
8 BAA02g38670 A02 32923757 C T upstream_gene_variant MODIFIER c.-925C>T| S122
9 BAA02g38670 A02 32924637 C T upstream_gene_variant MODIFIER c.-45C>T| S296
S85
10 BAA02g38670 A02 32924644 C T upstream_gene_variant MODIFIER c.-38C>T| S108
11 BAA02g38670 A02 32924775 G A missense_variant MODERATE c.94G>A|p.Asp32Asn S166
12 BAA02g38670 A02 32924848 C T missense_variant MODERATE c.167C>T|p.Ala56Val S303
13 BAA02g38670 A02 32924944 C T missense_variant MODERATE c.263C>T|p.Ser88Leu S280
14 BAA02g38670 A02 32924947 C T missense_variant MODERATE c.266C>T|p.Thr89Ile S283
15 BAA02g38670 A02 32924975 C T synonymous_variant LOW c.294C>T|p.Asn98Asn S234
16 BAA02g38670 A02 32925138 C T intron_variant MODIFIER c.428+29C>T| S286
17 BAA02g38670 A02 32925176 C T missense_variant MODERATE c.436C>T|p.Pro146Ser S112
18 BAA02g38670 A02 32926229 G A missense_variant MODERATE c.682G>A|p.Glu228Lys S199
19 BAA02g38670 A02 32926232 G A missense_variant MODERATE c.685G>A|p.Ala229Thr S221
20 BAA02g38670 A02 32929107 C T downstream_gene_variant MODIFIER c.*28C>T| S212
21 BAA02g38670 A02 32929332 C T downstream_gene_variant MODIFIER c.*253C>T| S193
22 BAA02g38670 A02 32929432 C T downstream_gene_variant MODIFIER c.*353C>T| S149
23 BAA02g38670 A02 32929519 C T downstream_gene_variant MODIFIER c.*440C>T| S112
24 BAA02g38670 A02 32929803 C T downstream_gene_variant MODIFIER c.*724C>T| S121
25 BAA02g38670 A02 32930082 C T downstream_gene_variant MODIFIER c.*1003C>T| S193