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
130451 BAA10g18030 A10 17081185 G A missense_variant MODERATE c.1024G>A|p.Asp342Asn S69
130452 BAA10g18030 A10 17081790 C T synonymous_variant LOW c.1629C>T|p.Thr543Thr S18
130453 BAA10g18040 A10 17082271 G A upstream_gene_variant MODIFIER c.-1255G>A| S207
130454 BAA10g18040 A10 17082996 G A upstream_gene_variant MODIFIER c.-530G>A| S292
130455 BAA10g18040 A10 17083485 C T upstream_gene_variant MODIFIER c.-41C>T| S124
130456 BAA10g18050 A10 17083779 C T upstream_gene_variant MODIFIER c.-621C>T| S246
130457 BAA10g18040 A10 17083851 G A missense_variant MODERATE c.226G>A|p.Gly76Ser S139
130458 BAA10g18050 A10 17084220 G A upstream_gene_variant MODIFIER c.-180G>A| S4
130459 BAA10g18050 A10 17084903 G A synonymous_variant LOW c.504G>A|p.Leu168Leu S72
S78
130460 BAA10g18060 A10 17085580 G A upstream_gene_variant MODIFIER c.-3031G>A| S35
130461 BAA10g18060 A10 17086225 C T upstream_gene_variant MODIFIER c.-2386C>T| S10
130462 BAA10g18060 A10 17086559 C T upstream_gene_variant MODIFIER c.-2052C>T| S68
130463 BAA10g18060 A10 17086644 G A upstream_gene_variant MODIFIER c.-1967G>A| S3
130464 BAA10g18060 A10 17086814 C T upstream_gene_variant MODIFIER c.-1797C>T| S256
130465 BAA10g18060 A10 17087728 G A upstream_gene_variant MODIFIER c.-883G>A| S234
130466 BAA10g18060 A10 17087824 C T upstream_gene_variant MODIFIER c.-787C>T| S201
130467 BAA10g18060 A10 17089291 C T synonymous_variant LOW c.681C>T|p.Val227Val S201
130468 BAA10g18060 A10 17089755 G A missense_variant MODERATE c.1145G>A|p.Arg382Lys S228
130469 BAA10g18060 A10 17089823 G A missense_variant MODERATE c.1213G>A|p.Val405Met S98
130470 BAA10g18060 A10 17089862 C T missense_variant MODERATE c.1252C>T|p.Leu418Phe S277
130471 BAA10g18060 A10 17090023 C T synonymous_variant LOW c.1413C>T|p.Leu471Leu S199
130472 BAA10g18060 A10 17090104 G A synonymous_variant LOW c.1494G>A|p.Arg498Arg S265
130473 BAA10g18060 A10 17090189 G A missense_variant MODERATE c.1579G>A|p.Ala527Thr S59
130474 BAA10g18060 A10 17090236 C T synonymous_variant LOW c.1626C>T|p.Tyr542Tyr S26
130475 BAA10g18070 A10 17091698 G A upstream_gene_variant MODIFIER c.-1201G>A| S219
S72