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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g05120 A01 2249431 C T missense_variant MODERATE c.199C>T|p.Leu67Phe S264
2 BAA01g05120 A01 2249445 C T synonymous_variant LOW c.213C>T|p.Val71Val S244
3 BAA01g05120 A01 2250479 G A stop_gained HIGH c.1178G>A|p.Trp393* S37
4 BAA01g05120 A01 2250955 G A missense_variant MODERATE c.1444G>A|p.Asp482Asn S224
5 BAA01g05120 A01 2251589 C T missense_variant MODERATE c.1985C>T|p.Thr662Ile S140
6 BAA01g05120 A01 2251939 G A missense_variant MODERATE c.2335G>A|p.Asp779Asn S208
S219
7 BAA01g05120 A01 2252040 G A synonymous_variant LOW c.2436G>A|p.Thr812Thr S105
S106
8 BAA01g05120 A01 2252941 G A missense_variant MODERATE c.2896G>A|p.Ala966Thr S204
9 BAA01g05120 A01 2253744 G A missense_variant MODERATE c.3278G>A|p.Gly1093Glu S242
10 BAA01g05120 A01 2253908 C T missense_variant MODERATE c.3442C>T|p.Leu1148Phe S246
11 BAA01g05120 A01 2254154 C T missense_variant MODERATE c.3688C>T|p.Pro1230Ser S164
12 BAA01g05120 A01 2254266 C T missense_variant MODERATE c.3800C>T|p.Pro1267Leu S66
13 BAA01g05120 A01 2254276 C T synonymous_variant LOW c.3810C>T|p.Tyr1270Tyr S221
14 BAA01g05120 A01 2254806 G A missense_variant MODERATE c.4340G>A|p.Arg1447Lys S175