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 BAA02g42540 A02 35419664 C T upstream_gene_variant MODIFIER c.-2869C>T| S9
2 BAA02g42540 A02 35419907 G A upstream_gene_variant MODIFIER c.-2626G>A| S45
3 BAA02g42540 A02 35419947 G A upstream_gene_variant MODIFIER c.-2586G>A| S149
4 BAA02g42540 A02 35421906 C T upstream_gene_variant MODIFIER c.-627C>T| S190
5 BAA02g42540 A02 35422418 C T upstream_gene_variant MODIFIER c.-115C>T| S182
6 BAA02g42540 A02 35424397 C T intron_variant MODIFIER c.153+1618C>T| S16
7 BAA02g42540 A02 35424502 G A intron_variant MODIFIER c.153+1723G>A| S84
S93
8 BAA02g42540 A02 35424511 C T intron_variant MODIFIER c.153+1732C>T| S131
9 BAA02g42540 A02 35426107 G A intron_variant MODIFIER c.154-2776G>A| S70
10 BAA02g42540 A02 35426112 C T intron_variant MODIFIER c.154-2771C>T| S256
11 BAA02g42540 A02 35426301 G A intron_variant MODIFIER c.154-2582G>A| S84
S93
12 BAA02g42540 A02 35426812 C T intron_variant MODIFIER c.154-2071C>T| S66
13 BAA02g42540 A02 35426851 C T intron_variant MODIFIER c.154-2032C>T| S130
14 BAA02g42540 A02 35426998 C T intron_variant MODIFIER c.154-1885C>T| S190
15 BAA02g42540 A02 35427085 G A intron_variant MODIFIER c.154-1798G>A| S251
16 BAA02g42540 A02 35427145 G A intron_variant MODIFIER c.154-1738G>A| S53
17 BAA02g42540 A02 35427295 C T intron_variant MODIFIER c.154-1588C>T| S18
18 BAA02g42540 A02 35427325 C T intron_variant MODIFIER c.154-1558C>T| S153
S213
19 BAA02g42540 A02 35427668 G A intron_variant MODIFIER c.154-1215G>A| S132
S137
S215
S89
20 BAA02g42540 A02 35428876 C T splice_region_variant&intron_variant LOW c.154-7C>T| S107
21 BAA02g42540 A02 35430272 G A synonymous_variant LOW c.852G>A|p.Arg284Arg S81
S85
22 BAA02g42540 A02 35431041 G A synonymous_variant LOW c.1128G>A|p.Arg376Arg S25
23 BAA02g42540 A02 35431153 C T missense_variant MODERATE c.1240C>T|p.Pro414Ser S33
24 BAA02g42540 A02 35431462 G A missense_variant MODERATE c.1549G>A|p.Ala517Thr S161
25 BAA02g42540 A02 35431489 G A missense_variant MODERATE c.1576G>A|p.Asp526Asn S37