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 BAA01g20840 A01 10269361 C T missense_variant MODERATE c.86C>T|p.Ser29Phe S170
2 BAA01g20840 A01 10269466 C T missense_variant MODERATE c.191C>T|p.Ser64Phe S69
3 BAA01g20840 A01 10269531 G A missense_variant MODERATE c.256G>A|p.Ala86Thr S291
4 BAA01g20840 A01 10269702 C T missense_variant MODERATE c.427C>T|p.Pro143Ser S146
5 BAA01g20840 A01 10269754 G T missense_variant MODERATE c.479G>T|p.Arg160Met S4
S6
6 BAA01g20840 A01 10270359 G A missense_variant MODERATE c.1084G>A|p.Glu362Lys S245
S294
7 BAA01g20840 A01 10270719 G A missense_variant MODERATE c.1444G>A|p.Val482Ile S203
8 BAA01g20840 A01 10270758 C T missense_variant MODERATE c.1483C>T|p.Pro495Ser S198
9 BAA01g20840 A01 10271770 G A stop_gained HIGH c.2061G>A|p.Trp687* S116
10 BAA01g20840 A01 10272141 C T missense_variant MODERATE c.2432C>T|p.Ser811Phe S247
11 BAA01g20840 A01 10273312 C T missense_variant MODERATE c.2848C>T|p.Leu950Phe S164
12 BAA01g20840 A01 10273422 G A stop_gained HIGH c.2958G>A|p.Trp986* S57
13 BAA01g20840 A01 10274186 C T missense_variant MODERATE c.3722C>T|p.Thr1241Ile S84
S93
14 BAA01g20840 A01 10274386 C T missense_variant MODERATE c.3922C>T|p.Pro1308Ser S38