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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g04620 A07 3813205 C T upstream_gene_variant MODIFIER c.-3240C>T| S100
2 BAA07g04620 A07 3815953 G A upstream_gene_variant MODIFIER c.-492G>A| S157
3 BAA07g04620 A07 3816156 G A upstream_gene_variant MODIFIER c.-289G>A| S257
4 BAA07g04620 A07 3816693 C T splice_region_variant&intron_variant LOW c.157-4C>T| S156
5 BAA07g04620 A07 3816696 G A splice_acceptor_variant&intron_variant HIGH c.157-1G>A| S175
6 BAA07g04620 A07 3817529 G A missense_variant MODERATE c.989G>A|p.Arg330His S159
S243
S299
S95
7 BAA07g04620 A07 3817535 C T missense_variant MODERATE c.995C>T|p.Pro332Leu S277
8 BAA07g04620 A07 3817590 C T synonymous_variant LOW c.1050C>T|p.Tyr350Tyr S1
S90
9 BAA07g04620 A07 3817600 G A missense_variant MODERATE c.1060G>A|p.Val354Met S40
S49
10 BAA07g04620 A07 3817993 G A missense_variant MODERATE c.1453G>A|p.Gly485Arg S266
11 BAA07g04620 A07 3819682 C T downstream_gene_variant MODIFIER c.*1525C>T| S56
12 BAA07g04620 A07 3819780 C A downstream_gene_variant MODIFIER c.*1623C>A| S128
13 BAA07g04620 A07 3821224 C T downstream_gene_variant MODIFIER c.*3067C>T| S213
14 BAA07g04620 A07 3822106 G A downstream_gene_variant MODIFIER c.*3949G>A| S33
15 BAA07g04620 A07 3822499 C T downstream_gene_variant MODIFIER c.*4342C>T| S52
16 BAA07g04620 A07 3822825 C T downstream_gene_variant MODIFIER c.*4668C>T| S153