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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g17760 A10 16954489 C T upstream_gene_variant MODIFIER c.-2559C>T| S283
2 BAA10g17760 A10 16954947 C T upstream_gene_variant MODIFIER c.-2101C>T| S25
3 BAA10g17760 A10 16954948 G A upstream_gene_variant MODIFIER c.-2100G>A| S167
4 BAA10g17760 A10 16955583 G A upstream_gene_variant MODIFIER c.-1465G>A| S131
5 BAA10g17760 A10 16956009 G A upstream_gene_variant MODIFIER c.-1039G>A| S178
6 BAA10g17760 A10 16956082 C T upstream_gene_variant MODIFIER c.-966C>T| S92
7 BAA10g17760 A10 16956532 C T upstream_gene_variant MODIFIER c.-516C>T| S187
8 BAA10g17760 A10 16956707 G A upstream_gene_variant MODIFIER c.-341G>A| S139
9 BAA10g17760 A10 16957771 G A stop_gained HIGH c.534G>A|p.Trp178* S264
10 BAA10g17760 A10 16958304 C T synonymous_variant LOW c.762C>T|p.Val254Val S281
11 BAA10g17760 A10 16958424 C T splice_region_variant&intron_variant LOW c.874+8C>T| S149
12 BAA10g17760 A10 16958677 C T synonymous_variant LOW c.1038C>T|p.Val346Val S46
13 BAA10g17760 A10 16958695 G A synonymous_variant LOW c.1056G>A|p.Leu352Leu S88
14 BAA10g17760 A10 16958830 G A synonymous_variant LOW c.1101G>A|p.Arg367Arg S181
15 BAA10g17760 A10 16958977 C T splice_region_variant&intron_variant LOW c.1162-4C>T| S173
16 BAA10g17760 A10 16959548 C T missense_variant MODERATE c.1466C>T|p.Ser489Phe S203
17 BAA10g17760 A10 16962205 C T downstream_gene_variant MODIFIER c.*384C>T| S81
S85