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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g14920 A01 7066571 G A synonymous_variant LOW c.6459C>T|p.Asn2153Asn S274
2 BAA01g14920 A01 7067336 G A missense_variant MODERATE c.5897C>T|p.Pro1966Leu S306
S308
3 BAA01g14920 A01 7068687 G A splice_region_variant&intron_variant LOW c.5069-6C>T| S116
4 BAA01g14920 A01 7070020 C T missense_variant MODERATE c.4307G>A|p.Ser1436Asn S25
5 BAA01g14920 A01 7070504 G A synonymous_variant LOW c.4195C>T|p.Leu1399Leu S256
6 BAA01g14920 A01 7070569 C T missense_variant MODERATE c.4130G>A|p.Gly1377Glu S151
S157
S166
S167
S262
S263
7 BAA01g14920 A01 7070938 C T missense_variant MODERATE c.3761G>A|p.Cys1254Tyr S54
8 BAA01g14920 A01 7071019 G A missense_variant MODERATE c.3680C>T|p.Ser1227Phe S245
9 BAA01g14920 A01 7074138 G A intron_variant MODIFIER c.1651-19C>T| S57
10 BAA01g14920 A01 7074242 G A synonymous_variant LOW c.1635C>T|p.Thr545Thr S181
11 BAA01g14920 A01 7074343 G A intron_variant MODIFIER c.1545-11C>T| S168
12 BAA01g14920 A01 7074354 G A intron_variant MODIFIER c.1545-22C>T| S178
13 BAA01g14920 A01 7074662 G A intron_variant MODIFIER c.1544+22C>T| S268
14 BAA01g14920 A01 7075406 G A intron_variant MODIFIER c.946-47C>T| S187
15 BAA01g14920 A01 7075552 G A missense_variant MODERATE c.922C>T|p.Arg308Cys S37
16 BAA01g14920 A01 7075757 T C missense_variant MODERATE c.803A>G|p.Tyr268Cys S6
17 BAA01g14920 A01 7076546 G A missense_variant MODERATE c.101C>T|p.Ser34Phe S40
S49
18 BAA01g14920 A01 7078295 C T upstream_gene_variant MODIFIER c.-1649G>A| S247
19 BAA01g14920 A01 7080046 C T upstream_gene_variant MODIFIER c.-3400G>A| S13
S278
S279
S64
20 BAA01g14920 A01 7080857 C T upstream_gene_variant MODIFIER c.-4211G>A| S179
21 BAA01g14920 A01 7081451 C T upstream_gene_variant MODIFIER c.-4805G>A| S18
22 BAA01g14920 A01 7081503 C T upstream_gene_variant MODIFIER c.-4857G>A| S18
23 BAA01g14920 A01 7081591 C T upstream_gene_variant MODIFIER c.-4945G>A| S20