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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g15900 A01 7731117 C T upstream_gene_variant MODIFIER c.-4871C>T| S10
2 BAA01g15900 A01 7733501 C T upstream_gene_variant MODIFIER c.-2487C>T| S226
3 BAA01g15900 A01 7734199 C T upstream_gene_variant MODIFIER c.-1789C>T| S231
4 BAA01g15900 A01 7734423 C T upstream_gene_variant MODIFIER c.-1565C>T| S182
5 BAA01g15900 A01 7735787 C T upstream_gene_variant MODIFIER c.-201C>T| S286
6 BAA01g15900 A01 7736153 G A intron_variant MODIFIER c.122-37G>A| S95
7 BAA01g15900 A01 7736671 G A missense_variant MODERATE c.397G>A|p.Asp133Asn S173
8 BAA01g15900 A01 7736800 C T intron_variant MODIFIER c.434-24C>T| S159
S243
9 BAA01g15900 A01 7736915 C T synonymous_variant LOW c.525C>T|p.Ser175Ser S136
10 BAA01g15900 A01 7737193 G A intron_variant MODIFIER c.591-147G>A| S72
S78
11 BAA01g15900 A01 7737706 C T intron_variant MODIFIER c.673-100C>T| S169
12 BAA01g15900 A01 7738940 G A intron_variant MODIFIER c.957+608G>A| S301
S304
13 BAA01g15900 A01 7739165 G A intron_variant MODIFIER c.957+833G>A| S156
14 BAA01g15900 A01 7739444 G A intron_variant MODIFIER c.957+1112G>A| S262
15 BAA01g15900 A01 7740006 C T intron_variant MODIFIER c.957+1674C>T| S16
16 BAA01g15900 A01 7740604 C T intron_variant MODIFIER c.957+2272C>T| S25
17 BAA01g15900 A01 7742720 C T intron_variant MODIFIER c.958-1908C>T| S159
S243
18 BAA01g15900 A01 7743550 C T intron_variant MODIFIER c.958-1078C>T| S303
19 BAA01g15900 A01 7743749 C T intron_variant MODIFIER c.958-879C>T| S130
20 BAA01g15900 A01 7745137 C T missense_variant MODERATE c.1094C>T|p.Ser365Leu S166
21 BAA01g15900 A01 7745357 G A synonymous_variant LOW c.1314G>A|p.Lys438Lys S178
22 BAA01g15900 A01 7745456 C T synonymous_variant LOW c.1413C>T|p.His471His S153
23 BAA01g15900 A01 7745695 C T missense_variant MODERATE c.1652C>T|p.Thr551Ile S98
24 BAA01g15900 A01 7746253 C T downstream_gene_variant MODIFIER c.*182C>T| S44