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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g10160 A02 4503726 C A upstream_gene_variant MODIFIER c.-4772C>A| S262
2 BAA02g10160 A02 4504012 G A upstream_gene_variant MODIFIER c.-4486G>A| S282
3 BAA02g10160 A02 4504063 C T upstream_gene_variant MODIFIER c.-4435C>T| S289
S290
4 BAA02g10160 A02 4504677 G A upstream_gene_variant MODIFIER c.-3821G>A| S203
5 BAA02g10160 A02 4505849 C T upstream_gene_variant MODIFIER c.-2649C>T| S263
6 BAA02g10160 A02 4506395 G A upstream_gene_variant MODIFIER c.-2103G>A| S168
7 BAA02g10160 A02 4508634 C T missense_variant MODERATE c.137C>T|p.Thr46Ile S242
8 BAA02g10160 A02 4509130 G A stop_gained HIGH c.633G>A|p.Trp211* S263
9 BAA02g10160 A02 4509498 G A missense_variant MODERATE c.1001G>A|p.Ser334Asn S197
10 BAA02g10160 A02 4509527 C T stop_gained HIGH c.1030C>T|p.Gln344* S240
11 BAA02g10160 A02 4511180 G A intron_variant MODIFIER c.1680+1003G>A| S302
12 BAA02g10160 A02 4511296 C T intron_variant MODIFIER c.1681-1045C>T| S224
13 BAA02g10160 A02 4511347 G A intron_variant MODIFIER c.1681-994G>A| S166
14 BAA02g10160 A02 4511426 C T intron_variant MODIFIER c.1681-915C>T| S73
S91
15 BAA02g10160 A02 4511456 G A intron_variant MODIFIER c.1681-885G>A| S303
16 BAA02g10160 A02 4511464 C T intron_variant MODIFIER c.1681-877C>T| S240
17 BAA02g10160 A02 4514982 C T synonymous_variant LOW c.2686C>T|p.Leu896Leu S175
18 BAA02g10160 A02 4515233 G A missense_variant MODERATE c.2937G>A|p.Met979Ile S283
19 BAA02g10160 A02 4516948 C T downstream_gene_variant MODIFIER c.*1067C>T| S25
S264
20 BAA02g10160 A02 4520509 G A downstream_gene_variant MODIFIER c.*4628G>A| S192