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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g41950 A07 36619179 G A intron_variant MODIFIER c.867-3068C>T| S288
2 BAA07g41950 A07 36619198 G T intron_variant MODIFIER c.867-3087C>A| S219
S72
3 BAA07g41950 A07 36620788 G A intron_variant MODIFIER c.867-4677C>T| S270
4 BAA07g41950 A07 36621085 C T intron_variant MODIFIER c.867-4974G>A| S221
5 BAA07g41950 A07 36621767 C T intron_variant MODIFIER c.866+4853G>A| S62
6 BAA07g41950 A07 36623488 C T intron_variant MODIFIER c.866+3132G>A| S283
7 BAA07g41950 A07 36624915 G A intron_variant MODIFIER c.866+1705C>T| S184
8 BAA07g41950 A07 36625024 G A intron_variant MODIFIER c.866+1596C>T| S110
9 BAA07g41950 A07 36625484 G A intron_variant MODIFIER c.866+1136C>T| S291
10 BAA07g41950 A07 36626250 G A intron_variant MODIFIER c.866+370C>T| S208
S219
11 BAA07g41950 A07 36627961 G A intron_variant MODIFIER c.371+12C>T| S134
12 BAA07g41950 A07 36628023 G A synonymous_variant LOW c.321C>T|p.Phe107Phe S298
13 BAA07g41950 A07 36628086 C T synonymous_variant LOW c.258G>A|p.Glu86Glu S221
14 BAA07g41950 A07 36628212 C T synonymous_variant LOW c.132G>A|p.Val44Val S18
15 BAA07g41950 A07 36628748 C T upstream_gene_variant MODIFIER c.-405G>A| S125
16 BAA07g41950 A07 36628912 C T upstream_gene_variant MODIFIER c.-569G>A| S68
17 BAA07g41950 A07 36629316 A G upstream_gene_variant MODIFIER c.-973T>C| S287
18 BAA07g41950 A07 36629666 G A upstream_gene_variant MODIFIER c.-1323C>T| S48
19 BAA07g41950 A07 36630894 G A upstream_gene_variant MODIFIER c.-2551C>T| S50
20 BAA07g41950 A07 36632404 C T upstream_gene_variant MODIFIER c.-4061G>A| S284
21 BAA07g41950 A07 36632966 G A upstream_gene_variant MODIFIER c.-4623C>T| S281
S282
22 BAA07g41950 A07 36633082 G A upstream_gene_variant MODIFIER c.-4739C>T| S171