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 BAA08g07760 A08 7066736 C T downstream_gene_variant MODIFIER c.*1237G>A| S184
2 BAA08g07760 A08 7067029 C T downstream_gene_variant MODIFIER c.*944G>A| S191
3 BAA08g07760 A08 7067314 G A downstream_gene_variant MODIFIER c.*659C>T| S10
4 BAA08g07760 A08 7068377 C T missense_variant MODERATE c.2788G>A|p.Asp930Asn S169
5 BAA08g07760 A08 7068404 C T missense_variant MODERATE c.2761G>A|p.Val921Met S223
6 BAA08g07760 A08 7068459 G A synonymous_variant LOW c.2706C>T|p.Thr902Thr S263
7 BAA08g07760 A08 7068745 C T stop_gained HIGH c.2616G>A|p.Trp872* S247
8 BAA08g07760 A08 7068907 G A missense_variant MODERATE c.2536C>T|p.Pro846Ser S20
9 BAA08g07760 A08 7069267 C T missense_variant MODERATE c.2176G>A|p.Glu726Lys S170
10 BAA08g07760 A08 7070443 G A stop_gained HIGH c.1531C>T|p.Gln511* S245
11 BAA08g07760 A08 7071114 G A missense_variant MODERATE c.950C>T|p.Ala317Val S287
12 BAA08g07760 A08 7071253 G A synonymous_variant LOW c.811C>T|p.Leu271Leu S119
13 BAA08g07760 A08 7071581 G A synonymous_variant LOW c.483C>T|p.Phe161Phe S103
14 BAA08g07760 A08 7071724 G A synonymous_variant LOW c.388C>T|p.Leu130Leu S107
15 BAA08g07760 A08 7073010 G A upstream_gene_variant MODIFIER c.-801C>T| S257
16 BAA08g07760 A08 7073332 C T upstream_gene_variant MODIFIER c.-1123G>A| S67
17 BAA08g07760 A08 7074422 C T upstream_gene_variant MODIFIER c.-2213G>A| S163
18 BAA08g07760 A08 7074996 C T upstream_gene_variant MODIFIER c.-2787G>A| S15
S156
S3
S34
S6
19 BAA08g07760 A08 7075043 G A upstream_gene_variant MODIFIER c.-2834C>T| S181
20 BAA08g07760 A08 7075484 G A upstream_gene_variant MODIFIER c.-3275C>T| S103
21 BAA08g07760 A08 7076596 C T upstream_gene_variant MODIFIER c.-4387G>A| S111
22 BAA08g07760 A08 7076773 C T upstream_gene_variant MODIFIER c.-4564G>A| S259
23 BAA08g07760 A08 7077078 C T upstream_gene_variant MODIFIER c.-4869G>A| S223
24 BAA08g07760 A08 7077160 G A upstream_gene_variant MODIFIER c.-4951C>T| S16