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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g12690 A01 5987272 G A upstream_gene_variant MODIFIER c.-4264G>A| S138
2 BAA01g12690 A01 5987387 G A upstream_gene_variant MODIFIER c.-4149G>A| S293
3 BAA01g12690 A01 5987634 G A upstream_gene_variant MODIFIER c.-3902G>A| S181
4 BAA01g12690 A01 5989010 G A upstream_gene_variant MODIFIER c.-2526G>A| S280
5 BAA01g12690 A01 5989084 G A upstream_gene_variant MODIFIER c.-2452G>A| S245
6 BAA01g12690 A01 5989722 C T upstream_gene_variant MODIFIER c.-1814C>T| S35
7 BAA01g12690 A01 5990128 G A upstream_gene_variant MODIFIER c.-1408G>A| S236
8 BAA01g12690 A01 5991523 C T upstream_gene_variant MODIFIER c.-13C>T| S78
9 BAA01g12690 A01 5991741 G A missense_variant MODERATE c.206G>A|p.Arg69His S133
10 BAA01g12690 A01 5991871 G A synonymous_variant LOW c.336G>A|p.Lys112Lys S28
11 BAA01g12690 A01 5992485 G A missense_variant MODERATE c.950G>A|p.Gly317Glu S257
12 BAA01g12690 A01 5992566 C T missense_variant MODERATE c.1031C>T|p.Thr344Ile S289
S290
13 BAA01g12690 A01 5992665 G A missense_variant MODERATE c.1130G>A|p.Gly377Glu S142
14 BAA01g12690 A01 5992874 C T missense_variant MODERATE c.1339C>T|p.Pro447Ser S136
15 BAA01g12690 A01 5993592 C T synonymous_variant LOW c.1671C>T|p.Ala557Ala S198
16 BAA01g12690 A01 5993691 C T downstream_gene_variant MODIFIER c.*63C>T| S135
17 BAA01g12690 A01 5993707 C T downstream_gene_variant MODIFIER c.*79C>T| S108
18 BAA01g12690 A01 5995252 C T downstream_gene_variant MODIFIER c.*1624C>T| S140
19 BAA01g12690 A01 5995384 C T downstream_gene_variant MODIFIER c.*1756C>T| S112
20 BAA01g12690 A01 5996754 G A downstream_gene_variant MODIFIER c.*3126G>A| S203
21 BAA01g12690 A01 5997669 C T downstream_gene_variant MODIFIER c.*4041C>T| S249
22 BAA01g12690 A01 5998505 G A downstream_gene_variant MODIFIER c.*4877G>A| S272