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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
143701 BAA10g28450 A10 21801047 C T upstream_gene_variant MODIFIER c.-370G>A| S187
143702 BAA10g28450 A10 21801578 C T upstream_gene_variant MODIFIER c.-901G>A| S206
S26
143703 BAA10g28450 A10 21801801 G A upstream_gene_variant MODIFIER c.-1124C>T| S15
S3
143704 BAA10g28450 A10 21804179 C T upstream_gene_variant MODIFIER c.-3502G>A| S155
S211
143705 BAA10g28460 A10 21805841 C T missense_variant MODERATE c.131C>T|p.Ala44Val S19
143706 BAA10g28460 A10 21806003 C T missense_variant MODERATE c.293C>T|p.Pro98Leu S40
S49
143707 BAA10g28460 A10 21807202 C T missense_variant MODERATE c.1322C>T|p.Ser441Phe S257
143708 BAA10g28460 A10 21807297 C T synonymous_variant LOW c.1417C>T|p.Leu473Leu S185
143709 BAA10g28460 A10 21807874 A C intron_variant MODIFIER c.1663+254A>C| S116
S45
143710 BAA10g28460 A10 21808248 G A missense_variant MODERATE c.1724G>A|p.Gly575Glu S7
143711 BAA10g28470 A10 21808700 C T downstream_gene_variant MODIFIER c.*4183G>A| S33
143712 BAA10g28460 A10 21809550 G A downstream_gene_variant MODIFIER c.*79G>A| S264
143713 BAA10g28460 A10 21810560 C T downstream_gene_variant MODIFIER c.*1089C>T| S236
143714 BAA10g28480 A10 21810878 G A upstream_gene_variant MODIFIER c.-4838G>A| S60
143715 BAA10g28480 A10 21812801 G A upstream_gene_variant MODIFIER c.-2915G>A| S288
143716 BAA10g28470 A10 21813039 C T synonymous_variant LOW c.1398G>A|p.Leu466Leu S92
143717 BAA10g28480 A10 21813145 C T upstream_gene_variant MODIFIER c.-2571C>T| S295
143718 BAA10g28480 A10 21814223 G A upstream_gene_variant MODIFIER c.-1493G>A| S90
143719 BAA10g28480 A10 21814561 G A upstream_gene_variant MODIFIER c.-1155G>A| S252
143720 BAA10g28480 A10 21815913 C T splice_region_variant&intron_variant LOW c.109+4C>T| S206
S26
143721 BAA10g28470 A10 21816096 G A upstream_gene_variant MODIFIER c.-912C>T| S122
143722 BAA10g28480 A10 21816435 G A splice_acceptor_variant&intron_variant HIGH c.264-1G>A| S288
143723 BAA10g28480 A10 21817372 C T missense_variant MODERATE c.823C>T|p.Pro275Ser S20
143724 BAA10g28500 A10 21818999 C T synonymous_variant LOW c.147G>A|p.Arg49Arg S242
143725 BAA10g28470 A10 21819883 C T upstream_gene_variant MODIFIER c.-4699G>A| S30
S31