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 BAA01g27670 A01 16649235 T A upstream_gene_variant MODIFIER c.-2725T>A| S130
2 BAA01g27670 A01 16649359 G A upstream_gene_variant MODIFIER c.-2601G>A| S7
3 BAA01g27670 A01 16650335 C T upstream_gene_variant MODIFIER c.-1625C>T| S69
4 BAA01g27670 A01 16650975 G A upstream_gene_variant MODIFIER c.-985G>A| S123
5 BAA01g27670 A01 16651369 G A upstream_gene_variant MODIFIER c.-591G>A| S163
6 BAA01g27670 A01 16651677 C T upstream_gene_variant MODIFIER c.-283C>T| S162
7 BAA01g27670 A01 16651737 G A upstream_gene_variant MODIFIER c.-223G>A| S123
S43
8 BAA01g27670 A01 16652065 G A missense_variant MODERATE c.106G>A|p.Asp36Asn S246
S87
9 BAA01g27670 A01 16652999 C T missense_variant MODERATE c.1040C>T|p.Thr347Met S283
10 BAA01g27670 A01 16653134 C T missense_variant MODERATE c.1175C>T|p.Pro392Leu S143
11 BAA01g27670 A01 16653647 G A downstream_gene_variant MODIFIER c.*29G>A| S281
12 BAA01g27670 A01 16653755 C T downstream_gene_variant MODIFIER c.*137C>T| S18
13 BAA01g27670 A01 16653808 T A downstream_gene_variant MODIFIER c.*190T>A| S26
14 BAA01g27670 A01 16654595 G A downstream_gene_variant MODIFIER c.*977G>A| S45
15 BAA01g27670 A01 16654604 C T downstream_gene_variant MODIFIER c.*986C>T| S171
16 BAA01g27670 A01 16655188 C T downstream_gene_variant MODIFIER c.*1570C>T| S289
S290
17 BAA01g27670 A01 16655287 G A downstream_gene_variant MODIFIER c.*1669G>A| S121
18 BAA01g27670 A01 16655911 C A downstream_gene_variant MODIFIER c.*2293C>A| S283
19 BAA01g27670 A01 16656123 G A downstream_gene_variant MODIFIER c.*2505G>A| S288
20 BAA01g27670 A01 16656743 C T downstream_gene_variant MODIFIER c.*3125C>T| S53
21 BAA01g27670 A01 16657584 C T downstream_gene_variant MODIFIER c.*3966C>T| S284
22 BAA01g27670 A01 16658400 C T downstream_gene_variant MODIFIER c.*4782C>T| S19
23 BAA01g27670 A01 16658511 G A downstream_gene_variant MODIFIER c.*4893G>A| S187