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
148401 BAA10g32750 A10 23446419 C T upstream_gene_variant MODIFIER c.-1011G>A| S218
148402 BAA10g32770 A10 23447065 C T missense_variant MODERATE c.104C>T|p.Ala35Val S97
148403 BAA10g32770 A10 23447388 G A missense_variant MODERATE c.427G>A|p.Glu143Lys S66
148404 BAA10g32770 A10 23447946 G A missense_variant MODERATE c.985G>A|p.Gly329Arg S57
148405 BAA10g32770 A10 23448068 C T synonymous_variant LOW c.1107C>T|p.Asn369Asn S156
148406 BAA10g32770 A10 23448566 G A synonymous_variant LOW c.1605G>A|p.Thr535Thr S9
148407 BAA10g32750 A10 23449578 C T upstream_gene_variant MODIFIER c.-4170G>A| S103
148408 BAA10g32780 A10 23450018 G A synonymous_variant LOW c.9G>A|p.Ala3Ala S100
148409 BAA10g32780 A10 23450525 G A missense_variant MODERATE c.196G>A|p.Val66Ile S70
148410 BAA10g32770 A10 23451945 G A downstream_gene_variant MODIFIER c.*3196G>A| S1
S90
148411 BAA10g32780 A10 23453700 C T missense_variant MODERATE c.1571C>T|p.Ala524Val S87
148412 BAA10g32790 A10 23453782 C T upstream_gene_variant MODIFIER c.-3373C>T| S188
148413 BAA10g32780 A10 23453888 G A synonymous_variant LOW c.1656G>A|p.Arg552Arg S288
148414 BAA10g32790 A10 23453968 A C upstream_gene_variant MODIFIER c.-3187A>C| S126
148415 BAA10g32780 A10 23454408 C T missense_variant MODERATE c.1966C>T|p.Pro656Ser S229
148416 BAA10g32780 A10 23454752 C T missense_variant MODERATE c.2176C>T|p.Arg726Trp S295
148417 BAA10g32780 A10 23454960 G A missense_variant MODERATE c.2384G>A|p.Gly795Glu S103
148418 BAA10g32790 A10 23455680 C T upstream_gene_variant MODIFIER c.-1475C>T| S296
148419 BAA10g32790 A10 23456626 G T upstream_gene_variant MODIFIER c.-529G>T| S201
148420 BAA10g32790 A10 23457290 G A missense_variant MODERATE c.136G>A|p.Glu46Lys S160
148421 BAA10g32790 A10 23457399 G A missense_variant MODERATE c.245G>A|p.Gly82Glu S265
148422 BAA10g32790 A10 23457471 C T missense_variant MODERATE c.317C>T|p.Ser106Phe S236
148423 BAA10g32790 A10 23458011 G C missense_variant MODERATE c.857G>C|p.Arg286Pro S12
148424 BAA10g32790 A10 23458118 G A missense_variant MODERATE c.964G>A|p.Gly322Arg S255
148425 BAA10g32790 A10 23458421 C T missense_variant MODERATE c.1267C>T|p.Leu423Phe S166