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 BAA01g21960 A01 10931489 G A upstream_gene_variant MODIFIER c.-357G>A| S268
2 BAA01g21960 A01 10931674 C T upstream_gene_variant MODIFIER c.-172C>T| S148
S210
S30
S31
3 BAA01g21960 A01 10931717 G A upstream_gene_variant MODIFIER c.-129G>A| S174
S216
S241
S39
S96
4 BAA01g21960 A01 10931804 G A upstream_gene_variant MODIFIER c.-42G>A| S209
5 BAA01g21960 A01 10931990 C T missense_variant MODERATE c.145C>T|p.His49Tyr S69
6 BAA01g21960 A01 10932308 G A missense_variant MODERATE c.463G>A|p.Gly155Arg S187
7 BAA01g21960 A01 10935379 C T stop_gained HIGH c.832C>T|p.Gln278* S183
8 BAA01g21960 A01 10936274 G A missense_variant MODERATE c.1232G>A|p.Gly411Asp S274
9 BAA01g21960 A01 10936616 G A missense_variant&splice_region_variant MODERATE c.1258G>A|p.Gly420Arg S165
10 BAA01g21960 A01 10936674 C T missense_variant MODERATE c.1316C>T|p.Ser439Phe S273
11 BAA01g21960 A01 10936740 G A intron_variant MODIFIER c.1333-33G>A| S57
12 BAA01g21960 A01 10936838 G A synonymous_variant LOW c.1398G>A|p.Val466Val S188
13 BAA01g21960 A01 10936943 C T synonymous_variant LOW c.1503C>T|p.Asn501Asn S218
14 BAA01g21960 A01 10937571 G A splice_region_variant&synonymous_variant LOW c.1971G>A|p.Lys657Lys S92
15 BAA01g21960 A01 10938074 C T intron_variant MODIFIER c.2181+60C>T| S107
16 BAA01g21960 A01 10938909 C T downstream_gene_variant MODIFIER c.*69C>T| S221
17 BAA01g21960 A01 10942471 C T downstream_gene_variant MODIFIER c.*3631C>T| S18
18 BAA01g21960 A01 10942965 C T downstream_gene_variant MODIFIER c.*4125C>T| S251
S290
19 BAA01g21960 A01 10942980 G A downstream_gene_variant MODIFIER c.*4140G>A| S187