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


Gene ID

Results: 1 - 29 of 29 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g38960 A03 18070085 C T synonymous_variant LOW c.3429G>A|p.Lys1143Lys S94
2 BAA03g38960 A03 18070311 G A synonymous_variant LOW c.3276C>T|p.Thr1092Thr S5
3 BAA03g38960 A03 18070675 C T missense_variant MODERATE c.2912G>A|p.Gly971Glu S156
4 BAA03g38960 A03 18071564 G A intron_variant MODIFIER c.2729-706C>T| S184
5 BAA03g38960 A03 18072538 C T intron_variant MODIFIER c.2728+15G>A| S153
6 BAA03g38960 A03 18073684 C T missense_variant MODERATE c.2062G>A|p.Glu688Lys S221
7 BAA03g38960 A03 18073694 G A splice_region_variant&synonymous_variant LOW c.2052C>T|p.Leu684Leu S231
8 BAA03g38960 A03 18073993 G A missense_variant MODERATE c.1985C>T|p.Ala662Val S267
9 BAA03g38960 A03 18074083 C T intron_variant MODIFIER c.1977+16G>A| S155
10 BAA03g38960 A03 18074147 G A synonymous_variant LOW c.1929C>T|p.Asp643Asp S13
S140
S219
S279
S64
S72
11 BAA03g38960 A03 18074375 C T intron_variant MODIFIER c.1862+116G>A| S239
12 BAA03g38960 A03 18075419 C T stop_gained HIGH c.1359G>A|p.Trp453* S34
13 BAA03g38960 A03 18076527 C T missense_variant MODERATE c.859G>A|p.Val287Met S187
14 BAA03g38960 A03 18076575 G A intron_variant MODIFIER c.855-44C>T| S67
15 BAA03g38960 A03 18076594 C T intron_variant MODIFIER c.855-63G>A| S15
S3
16 BAA03g38960 A03 18076748 G A missense_variant MODERATE c.850C>T|p.Arg284Cys S271
17 BAA03g38960 A03 18076765 C T missense_variant MODERATE c.833G>A|p.Gly278Asp S116
18 BAA03g38960 A03 18076998 C T missense_variant MODERATE c.740G>A|p.Gly247Asp S38
19 BAA03g38960 A03 18077523 G A missense_variant MODERATE c.398C>T|p.Ala133Val S12
20 BAA03g38960 A03 18078833 C T upstream_gene_variant MODIFIER c.-148G>A| S155
S211
21 BAA03g38960 A03 18079227 G A upstream_gene_variant MODIFIER c.-542C>T| S115
22 BAA03g38960 A03 18079230 C T upstream_gene_variant MODIFIER c.-545G>A| S163
23 BAA03g38960 A03 18079999 G A upstream_gene_variant MODIFIER c.-1314C>T| S6
24 BAA03g38960 A03 18080100 C T upstream_gene_variant MODIFIER c.-1415G>A| S34
25 BAA03g38960 A03 18080349 G A upstream_gene_variant MODIFIER c.-1664C>T| S212