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
12601 BAA01g10010 A01 4521609 G A missense_variant MODERATE c.206G>A|p.Gly69Glu S116
12602 BAA01g10010 A01 4521639 G A missense_variant MODERATE c.236G>A|p.Arg79Lys S239
12603 BAA01g10010 A01 4522181 C T splice_region_variant&intron_variant LOW c.609+4C>T| S295
12604 BAA01g10000 A01 4522492 G A upstream_gene_variant MODIFIER c.-1845C>T| S162
12605 BAA01g10010 A01 4522817 C T missense_variant MODERATE c.992C>T|p.Ala331Val S166
12606 BAA01g10000 A01 4522907 G A upstream_gene_variant MODIFIER c.-2260C>T| S276
12607 BAA01g10000 A01 4522952 C T upstream_gene_variant MODIFIER c.-2305G>A| S132
S137
S215
12608 BAA01g10020 A01 4523363 G A missense_variant MODERATE c.542C>T|p.Ser181Phe S28
12609 BAA01g10020 A01 4523570 C T missense_variant&splice_region_variant MODERATE c.412G>A|p.Ala138Thr S264
12610 BAA01g10000 A01 4525423 C T upstream_gene_variant MODIFIER c.-4776G>A| S302
12611 BAA01g10020 A01 4525763 C T upstream_gene_variant MODIFIER c.-907G>A| S25
12612 BAA01g10020 A01 4526025 C T upstream_gene_variant MODIFIER c.-1169G>A| S99
12613 BAA01g10020 A01 4526031 G A upstream_gene_variant MODIFIER c.-1175C>T| S92
12614 BAA01g10020 A01 4526379 C T upstream_gene_variant MODIFIER c.-1523G>A| S148
S30
S31
12615 BAA01g10020 A01 4526477 C T upstream_gene_variant MODIFIER c.-1621G>A| S210
12616 BAA01g10020 A01 4526785 G A upstream_gene_variant MODIFIER c.-1929C>T| S173
12617 BAA01g10020 A01 4527091 C T upstream_gene_variant MODIFIER c.-2235G>A| S295
12618 BAA01g10020 A01 4527738 C T upstream_gene_variant MODIFIER c.-2882G>A| S39
12619 BAA01g10020 A01 4528013 C T upstream_gene_variant MODIFIER c.-3157G>A| S295
12620 BAA01g10030 A01 4528637 G A missense_variant MODERATE c.76G>A|p.Gly26Arg S180
12621 BAA01g10030 A01 4529069 G A missense_variant MODERATE c.280G>A|p.Asp94Asn S272
12622 BAA01g10030 A01 4529569 C T synonymous_variant LOW c.502C>T|p.Leu168Leu S205
12623 BAA01g10040 A01 4530857 C T missense_variant MODERATE c.1100G>A|p.Gly367Glu S185
12624 BAA01g10040 A01 4531068 G A missense_variant MODERATE c.965C>T|p.Ser322Leu S157
S163
12625 BAA01g10050 A01 4533402 G A synonymous_variant LOW c.729C>T|p.Ala243Ala S190