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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g19860 A10 18073637 C T upstream_gene_variant MODIFIER c.-3944C>T| S133
2 BAA10g19860 A10 18075059 C T upstream_gene_variant MODIFIER c.-2522C>T| S247
3 BAA10g19860 A10 18075182 C T upstream_gene_variant MODIFIER c.-2399C>T| S168
4 BAA10g19860 A10 18075241 C T upstream_gene_variant MODIFIER c.-2340C>T| S296
5 BAA10g19860 A10 18075272 C T upstream_gene_variant MODIFIER c.-2309C>T| S186
6 BAA10g19860 A10 18075424 C T upstream_gene_variant MODIFIER c.-2157C>T| S25
7 BAA10g19860 A10 18076210 C T upstream_gene_variant MODIFIER c.-1371C>T| S133
8 BAA10g19860 A10 18076502 G C upstream_gene_variant MODIFIER c.-1079G>C| S128
9 BAA10g19860 A10 18076635 C T upstream_gene_variant MODIFIER c.-946C>T| S173
10 BAA10g19860 A10 18076842 C T upstream_gene_variant MODIFIER c.-739C>T| S95
11 BAA10g19860 A10 18077804 G A missense_variant MODERATE c.124G>A|p.Glu42Lys S280
12 BAA10g19860 A10 18078300 G A missense_variant&splice_region_variant MODERATE c.367G>A|p.Glu123Lys S209
S221
13 BAA10g19860 A10 18078403 C T splice_region_variant&intron_variant LOW c.370-3C>T| S38
14 BAA10g19860 A10 18078708 G A missense_variant MODERATE c.583G>A|p.Asp195Asn S198
15 BAA10g19860 A10 18081308 C T downstream_gene_variant MODIFIER c.*1822C>T| S305
16 BAA10g19860 A10 18081795 C T downstream_gene_variant MODIFIER c.*2309C>T| S70
17 BAA10g19860 A10 18081893 C T downstream_gene_variant MODIFIER c.*2407C>T| S299