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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g18550 A10 17333527 C T downstream_gene_variant MODIFIER c.*1538G>A| S33
2 BAA10g18550 A10 17333579 C T downstream_gene_variant MODIFIER c.*1486G>A| S197
3 BAA10g18550 A10 17333744 C T downstream_gene_variant MODIFIER c.*1321G>A| S156
4 BAA10g18550 A10 17333858 C T downstream_gene_variant MODIFIER c.*1207G>A| S247
5 BAA10g18550 A10 17334534 C T downstream_gene_variant MODIFIER c.*531G>A| S103
6 BAA10g18550 A10 17334757 C T downstream_gene_variant MODIFIER c.*308G>A| S77
7 BAA10g18550 A10 17335444 C T missense_variant MODERATE c.1724G>A|p.Arg575His S51
8 BAA10g18550 A10 17335848 C T synonymous_variant LOW c.1320G>A|p.Lys440Lys S236
9 BAA10g18550 A10 17336118 G A synonymous_variant LOW c.1050C>T|p.Ser350Ser S221
10 BAA10g18550 A10 17336711 G A stop_gained HIGH c.457C>T|p.Gln153* S297
11 BAA10g18550 A10 17336880 G A synonymous_variant LOW c.288C>T|p.Ser96Ser S151
S263
12 BAA10g18550 A10 17337137 C T intron_variant MODIFIER c.211-180G>A| S183
13 BAA10g18550 A10 17338040 C T intron_variant MODIFIER c.210+804G>A| S232
14 BAA10g18550 A10 17338922 C T synonymous_variant LOW c.132G>A|p.Thr44Thr S283
15 BAA10g18550 A10 17339136 G A upstream_gene_variant MODIFIER c.-83C>T| S293
16 BAA10g18550 A10 17339191 G A upstream_gene_variant MODIFIER c.-138C>T| S63
17 BAA10g18550 A10 17339765 C T upstream_gene_variant MODIFIER c.-712G>A| S195
18 BAA10g18550 A10 17339994 G A upstream_gene_variant MODIFIER c.-941C>T| S198
19 BAA10g18550 A10 17340256 C T upstream_gene_variant MODIFIER c.-1203G>A| S23
20 BAA10g18550 A10 17341474 G A upstream_gene_variant MODIFIER c.-2421C>T| S293
21 BAA10g18550 A10 17342323 G A upstream_gene_variant MODIFIER c.-3270C>T| S216