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
126401 BAA10g15150 A10 15644202 C T upstream_gene_variant MODIFIER c.-4479G>A| S133
126402 BAA10g15150 A10 15644394 G A upstream_gene_variant MODIFIER c.-4671C>T| S160
126403 BAA10g15150 A10 15644568 C T upstream_gene_variant MODIFIER c.-4845G>A| S297
126404 BAA10g15150 A10 15644689 C T upstream_gene_variant MODIFIER c.-4966G>A| S305
126405 BAA10g15160 A10 15645077 G A upstream_gene_variant MODIFIER c.-2134C>T| S236
126406 BAA10g15170 A10 15645941 G A missense_variant MODERATE c.599G>A|p.Gly200Glu S292
126407 BAA10g15170 A10 15646040 G A missense_variant MODERATE c.698G>A|p.Arg233Lys S286
126408 BAA10g15160 A10 15646691 G A upstream_gene_variant MODIFIER c.-3748C>T| S72
S78
126409 BAA10g15160 A10 15646768 G A upstream_gene_variant MODIFIER c.-3825C>T| S62
126410 BAA10g15180 A10 15647378 C T synonymous_variant LOW c.306G>A|p.Glu102Glu S10
126411 BAA10g15180 A10 15647392 C T missense_variant MODERATE c.292G>A|p.Ala98Thr S242
126412 BAA10g15190 A10 15648896 G A synonymous_variant LOW c.630C>T|p.Ser210Ser S18
126413 BAA10g15180 A10 15649684 G A upstream_gene_variant MODIFIER c.-1856C>T| S176
126414 BAA10g15190 A10 15649701 C T stop_gained HIGH c.216G>A|p.Trp72* S54
126415 BAA10g15180 A10 15649839 G A upstream_gene_variant MODIFIER c.-2011C>T| S295
126416 BAA10g15180 A10 15651095 G A upstream_gene_variant MODIFIER c.-3267C>T| S47
126417 BAA10g15180 A10 15652231 C T upstream_gene_variant MODIFIER c.-4403G>A| S200
126418 BAA10g15200 A10 15653728 C T stop_gained HIGH c.1099C>T|p.Gln367* S275
126419 BAA10g15200 A10 15654754 G A missense_variant MODERATE c.1711G>A|p.Asp571Asn S50
126420 BAA10g15220 A10 15655232 C T upstream_gene_variant MODIFIER c.-3189C>T| S259
126421 BAA10g15200 A10 15655496 G A splice_acceptor_variant&intron_variant HIGH c.2053-1G>A| S223
126422 BAA10g15200 A10 15656203 G A splice_region_variant&intron_variant LOW c.2593+3G>A| S65
126423 BAA10g15220 A10 15656858 C T upstream_gene_variant MODIFIER c.-1563C>T| S33
126424 BAA10g15220 A10 15656990 C T upstream_gene_variant MODIFIER c.-1431C>T| S268
126425 BAA10g15220 A10 15657013 C T upstream_gene_variant MODIFIER c.-1408C>T| S38