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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g26100 A05 30793212 G T upstream_gene_variant MODIFIER c.-4005G>T| S134
2 BAA05g26100 A05 30793605 C T upstream_gene_variant MODIFIER c.-3612C>T| S174
3 BAA05g26100 A05 30794243 G A upstream_gene_variant MODIFIER c.-2974G>A| S50
4 BAA05g26100 A05 30794462 G A upstream_gene_variant MODIFIER c.-2755G>A| S152
5 BAA05g26100 A05 30794632 G A upstream_gene_variant MODIFIER c.-2585G>A| S64
6 BAA05g26100 A05 30794723 G A upstream_gene_variant MODIFIER c.-2494G>A| S54
7 BAA05g26100 A05 30795124 C T upstream_gene_variant MODIFIER c.-2093C>T| S183
S198
8 BAA05g26100 A05 30796786 G A upstream_gene_variant MODIFIER c.-431G>A| S308
9 BAA05g26100 A05 30796794 G A upstream_gene_variant MODIFIER c.-423G>A| S257
10 BAA05g26100 A05 30796798 C T upstream_gene_variant MODIFIER c.-419C>T| S37
11 BAA05g26100 A05 30797304 C T missense_variant MODERATE c.88C>T|p.Pro30Ser S195
12 BAA05g26100 A05 30797333 C T synonymous_variant LOW c.117C>T|p.Ile39Ile S67
13 BAA05g26100 A05 30797502 C T missense_variant MODERATE c.286C>T|p.Pro96Ser S119
S32
14 BAA05g26100 A05 30797743 G A missense_variant MODERATE c.527G>A|p.Gly176Glu S228
15 BAA05g26100 A05 30798035 G A synonymous_variant LOW c.819G>A|p.Glu273Glu S139
16 BAA05g26100 A05 30799412 G A synonymous_variant LOW c.1143G>A|p.Lys381Lys S15
S3
17 BAA05g26100 A05 30799653 G A missense_variant MODERATE c.1384G>A|p.Glu462Lys S45
18 BAA05g26100 A05 30800043 G A missense_variant MODERATE c.1606G>A|p.Gly536Arg S85
19 BAA05g26100 A05 30802602 G A downstream_gene_variant MODIFIER c.*2506G>A| S162
20 BAA05g26100 A05 30802603 G A downstream_gene_variant MODIFIER c.*2507G>A| S179
21 BAA05g26100 A05 30803332 C T downstream_gene_variant MODIFIER c.*3236C>T| S107
22 BAA05g26100 A05 30804260 G A downstream_gene_variant MODIFIER c.*4164G>A| S124
23 BAA05g26100 A05 30805070 G A downstream_gene_variant MODIFIER c.*4974G>A| S190
24 BAA05g26100 A05 30805078 C T downstream_gene_variant MODIFIER c.*4982C>T| S262