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
132851 BAA10g19570 A10 17911540 C T upstream_gene_variant MODIFIER c.-3989G>A| S117
132852 BAA10g19590 A10 17918422 G A upstream_gene_variant MODIFIER c.-2039G>A| S57
132853 BAA10g19590 A10 17919005 C T upstream_gene_variant MODIFIER c.-1456C>T| S169
132854 BAA10g19600 A10 17923558 C T downstream_gene_variant MODIFIER c.*2346G>A| S117
132855 BAA10g19590 A10 17923692 G A missense_variant MODERATE c.1682G>A|p.Gly561Glu S160
132856 BAA10g19590 A10 17923796 G A missense_variant MODERATE c.1786G>A|p.Ala596Thr S219
132857 BAA10g19590 A10 17924246 C T synonymous_variant LOW c.2025C>T|p.Cys675Cys S107
132858 BAA10g19590 A10 17924408 C T synonymous_variant LOW c.2100C>T|p.Phe700Phe S130
132859 BAA10g19600 A10 17924545 C T downstream_gene_variant MODIFIER c.*1359G>A| S136
132860 BAA10g19590 A10 17924722 G A missense_variant MODERATE c.2305G>A|p.Glu769Lys S280
132861 BAA10g19590 A10 17924904 G A missense_variant MODERATE c.2344G>A|p.Glu782Lys S67
132862 BAA10g19590 A10 17926145 G A downstream_gene_variant MODIFIER c.*1125G>A| S95
132863 BAA10g19600 A10 17927062 C T splice_acceptor_variant&intron_variant HIGH c.2130-1G>A| S115
132864 BAA10g19600 A10 17927219 G A splice_region_variant&intron_variant LOW c.2064-8C>T| S25
132865 BAA10g19590 A10 17927278 G A downstream_gene_variant MODIFIER c.*2258G>A| S273
132866 BAA10g19590 A10 17927900 G A downstream_gene_variant MODIFIER c.*2880G>A| S279
132867 BAA10g19600 A10 17929348 C T missense_variant MODERATE c.818G>A|p.Arg273Lys S51
132868 BAA10g19600 A10 17929511 C T missense_variant MODERATE c.736G>A|p.Asp246Asn S84
S93
132869 BAA10g19600 A10 17929709 C T missense_variant MODERATE c.641G>A|p.Arg214Lys S25
132870 BAA10g19600 A10 17930288 A G synonymous_variant LOW c.159T>C|p.Arg53Arg S62
132871 BAA10g19600 A10 17932620 G A upstream_gene_variant MODIFIER c.-1979C>T| S94
132872 BAA10g19600 A10 17934173 T A upstream_gene_variant MODIFIER c.-3532A>T| S63
132873 BAA10g19600 A10 17935604 C T upstream_gene_variant MODIFIER c.-4963G>A| S306
S308
132874 BAA10g19610 A10 17936454 G A downstream_gene_variant MODIFIER c.*1806C>T| S278
132875 BAA10g19610 A10 17939353 G A intron_variant MODIFIER c.2244-26C>T| S128