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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g17770 A01 8627585 C T missense_variant MODERATE c.236C>T|p.Ser79Phe S146
2 BAA01g17770 A01 8628316 G A missense_variant MODERATE c.967G>A|p.Gly323Arg S275
3 BAA01g17770 A01 8628572 G C missense_variant MODERATE c.1223G>C|p.Ser408Thr S262
4 BAA01g17770 A01 8630623 G A intron_variant MODIFIER c.1293+1981G>A| S129
5 BAA01g17770 A01 8630805 C T intron_variant MODIFIER c.1293+2163C>T| S247
6 BAA01g17770 A01 8631462 A T intron_variant MODIFIER c.1293+2820A>T| S149
7 BAA01g17770 A01 8631525 G A intron_variant MODIFIER c.1293+2883G>A| S212
8 BAA01g17770 A01 8631709 C T intron_variant MODIFIER c.1293+3067C>T| S177
9 BAA01g17770 A01 8633448 C T intron_variant MODIFIER c.1293+4806C>T| S113
10 BAA01g17770 A01 8633924 C T intron_variant MODIFIER c.1293+5282C>T| S44
11 BAA01g17770 A01 8634300 G A intron_variant MODIFIER c.1293+5658G>A| S40
S49
12 BAA01g17770 A01 8634355 C T intron_variant MODIFIER c.1293+5713C>T| S160
13 BAA01g17770 A01 8634441 C T intron_variant MODIFIER c.1293+5799C>T| S164
14 BAA01g17770 A01 8634551 T C intron_variant MODIFIER c.1293+5909T>C| S43
15 BAA01g17770 A01 8634699 C T intron_variant MODIFIER c.1293+6057C>T| S247
16 BAA01g17770 A01 8637618 C T intron_variant MODIFIER c.1294-7680C>T| S158
17 BAA01g17770 A01 8640034 C T intron_variant MODIFIER c.1294-5264C>T| S36
18 BAA01g17770 A01 8640102 C T intron_variant MODIFIER c.1294-5196C>T| S62
19 BAA01g17770 A01 8640106 C T intron_variant MODIFIER c.1294-5192C>T| S20
20 BAA01g17770 A01 8645511 C T missense_variant MODERATE c.1507C>T|p.Pro503Ser S302