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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g02690 A08 1883640 C T downstream_gene_variant MODIFIER c.*4100G>A| S275
2 BAA08g02690 A08 1883680 C T downstream_gene_variant MODIFIER c.*4060G>A| S6
3 BAA08g02690 A08 1884378 G A downstream_gene_variant MODIFIER c.*3362C>T| S239
4 BAA08g02690 A08 1884594 C T downstream_gene_variant MODIFIER c.*3146G>A| S302
5 BAA08g02690 A08 1884807 G A downstream_gene_variant MODIFIER c.*2933C>T| S221
6 BAA08g02690 A08 1884914 C T downstream_gene_variant MODIFIER c.*2826G>A| S57
7 BAA08g02690 A08 1884924 G A downstream_gene_variant MODIFIER c.*2816C>T| S210
S225
8 BAA08g02690 A08 1885005 G A downstream_gene_variant MODIFIER c.*2735C>T| S150
9 BAA08g02690 A08 1886957 G A downstream_gene_variant MODIFIER c.*783C>T| S221
10 BAA08g02690 A08 1887254 C T downstream_gene_variant MODIFIER c.*486G>A| S50
11 BAA08g02690 A08 1887900 G A missense_variant MODERATE c.944C>T|p.Ser315Phe S38
12 BAA08g02690 A08 1888040 G A synonymous_variant LOW c.804C>T|p.Asn268Asn S116
13 BAA08g02690 A08 1888109 C T synonymous_variant LOW c.735G>A|p.Lys245Lys S155
S211
14 BAA08g02690 A08 1888730 C T stop_gained HIGH c.114G>A|p.Trp38* S276
15 BAA08g02690 A08 1889024 T A upstream_gene_variant MODIFIER c.-181A>T| S257
16 BAA08g02690 A08 1889068 C T upstream_gene_variant MODIFIER c.-225G>A| S296
17 BAA08g02690 A08 1889300 C T upstream_gene_variant MODIFIER c.-457G>A| S169
18 BAA08g02690 A08 1890733 G A upstream_gene_variant MODIFIER c.-1890C>T| S202
19 BAA08g02690 A08 1892142 C T upstream_gene_variant MODIFIER c.-3299G>A| S172
S217