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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g19350 A05 11379784 C T upstream_gene_variant MODIFIER c.-2386C>T| S140
S278
S279
2 BAA05g19350 A05 11380063 G A upstream_gene_variant MODIFIER c.-2107G>A| S152
3 BAA05g19350 A05 11380097 G A upstream_gene_variant MODIFIER c.-2073G>A| S138
4 BAA05g19350 A05 11380415 G A upstream_gene_variant MODIFIER c.-1755G>A| S157
S163
5 BAA05g19350 A05 11380560 C G upstream_gene_variant MODIFIER c.-1610C>G| S32
6 BAA05g19350 A05 11380807 G A upstream_gene_variant MODIFIER c.-1363G>A| S66
7 BAA05g19350 A05 11381303 G A upstream_gene_variant MODIFIER c.-867G>A| S278
8 BAA05g19350 A05 11381313 G A upstream_gene_variant MODIFIER c.-857G>A| S256
9 BAA05g19350 A05 11381712 G A upstream_gene_variant MODIFIER c.-458G>A| S40
S49
10 BAA05g19350 A05 11382408 C T missense_variant MODERATE c.239C>T|p.Pro80Leu S305
11 BAA05g19350 A05 11382550 C T synonymous_variant LOW c.381C>T|p.Leu127Leu S235
12 BAA05g19350 A05 11383943 G A missense_variant MODERATE c.1067G>A|p.Gly356Asp S15
13 BAA05g19350 A05 11384637 C T synonymous_variant LOW c.1590C>T|p.Thr530Thr S136
14 BAA05g19350 A05 11384717 G A missense_variant MODERATE c.1670G>A|p.Gly557Glu S32
15 BAA05g19350 A05 11384798 G A missense_variant MODERATE c.1751G>A|p.Gly584Glu S161
16 BAA05g19350 A05 11384887 C T missense_variant MODERATE c.1840C>T|p.Arg614Trp S18
17 BAA05g19350 A05 11385680 G A downstream_gene_variant MODIFIER c.*269G>A| S199
18 BAA05g19350 A05 11385949 G A downstream_gene_variant MODIFIER c.*538G>A| S186
19 BAA05g19350 A05 11386096 C T downstream_gene_variant MODIFIER c.*685C>T| S211
20 BAA05g19350 A05 11386134 C T downstream_gene_variant MODIFIER c.*723C>T| S57
21 BAA05g19350 A05 11386202 C T downstream_gene_variant MODIFIER c.*791C>T| S88
22 BAA05g19350 A05 11386349 C T downstream_gene_variant MODIFIER c.*938C>T| S148
S30
S31
23 BAA05g19350 A05 11386377 C A downstream_gene_variant MODIFIER c.*966C>A| S178