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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g19790 A08 15481531 C T splice_acceptor_variant&intron_variant HIGH c.1654-1G>A| S197
2 BAA08g19790 A08 15483176 G A splice_region_variant&intron_variant LOW c.1170+8C>T| S81
S85
3 BAA08g19790 A08 15484095 G A splice_region_variant&intron_variant LOW c.873-4C>T| S259
4 BAA08g19790 A08 15485170 C T intron_variant MODIFIER c.872+184G>A| S34
5 BAA08g19790 A08 15485555 C A intron_variant MODIFIER c.775-104G>T| S47
6 BAA08g19790 A08 15485724 C T intron_variant MODIFIER c.775-273G>A| S169
7 BAA08g19790 A08 15485756 C T intron_variant MODIFIER c.775-305G>A| S123
8 BAA08g19790 A08 15486590 C T intron_variant MODIFIER c.775-1139G>A| S236
9 BAA08g19790 A08 15487056 G A intron_variant MODIFIER c.774+1370C>T| S70
10 BAA08g19790 A08 15487061 G A intron_variant MODIFIER c.774+1365C>T| S280
11 BAA08g19790 A08 15487425 G A intron_variant MODIFIER c.774+1001C>T| S84
S93
12 BAA08g19790 A08 15487506 G A intron_variant MODIFIER c.774+920C>T| S95
13 BAA08g19790 A08 15488790 G A missense_variant MODERATE c.410C>T|p.Ala137Val S1
S90
14 BAA08g19790 A08 15488857 C T missense_variant MODERATE c.343G>A|p.Gly115Ser S54
15 BAA08g19790 A08 15490040 C T upstream_gene_variant MODIFIER c.-212G>A| S89
16 BAA08g19790 A08 15490978 G A upstream_gene_variant MODIFIER c.-1150C>T| S97
17 BAA08g19790 A08 15491798 C T upstream_gene_variant MODIFIER c.-1970G>A| S28
18 BAA08g19790 A08 15493231 C T upstream_gene_variant MODIFIER c.-3403G>A| S175