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
115501 BAA10g09850 A10 11706773 C T upstream_gene_variant MODIFIER c.-1520G>A| S84
S93
115502 BAA10g09850 A10 11706927 G A upstream_gene_variant MODIFIER c.-1674C>T| S66
115503 BAA10g09850 A10 11707225 G A upstream_gene_variant MODIFIER c.-1972C>T| S250
115504 BAA10g09850 A10 11707505 G A upstream_gene_variant MODIFIER c.-2252C>T| S176
115505 BAA10g09850 A10 11708260 G A upstream_gene_variant MODIFIER c.-3007C>T| S1
S90
115506 BAA10g09850 A10 11708286 C T upstream_gene_variant MODIFIER c.-3033G>A| S17
115507 BAA10g09860 A10 11708370 G A splice_region_variant&synonymous_variant LOW c.24G>A|p.Ser8Ser S62
115508 BAA10g09850 A10 11708432 C T upstream_gene_variant MODIFIER c.-3179G>A| S131
115509 BAA10g09850 A10 11709299 C T upstream_gene_variant MODIFIER c.-4046G>A| S272
115510 BAA10g09870 A10 11710728 G A missense_variant MODERATE c.1628C>T|p.Pro543Leu S240
115511 BAA10g09870 A10 11710765 G A missense_variant MODERATE c.1591C>T|p.Pro531Ser S240
115512 BAA10g09870 A10 11711407 C T missense_variant MODERATE c.949G>A|p.Gly317Arg S244
115513 BAA10g09870 A10 11712404 C T synonymous_variant LOW c.258G>A|p.Arg86Arg S259
115514 BAA10g09870 A10 11713217 C T upstream_gene_variant MODIFIER c.-556G>A| S191
115515 BAA10g09870 A10 11714187 C T upstream_gene_variant MODIFIER c.-1526G>A| S239
115516 BAA10g09870 A10 11715057 G A upstream_gene_variant MODIFIER c.-2396C>T| S60
115517 BAA10g09870 A10 11715444 C T upstream_gene_variant MODIFIER c.-2783G>A| S170
115518 BAA10g09870 A10 11716506 C T upstream_gene_variant MODIFIER c.-3845G>A| S79
S91
115519 BAA10g09870 A10 11716860 A T upstream_gene_variant MODIFIER c.-4199T>A| S302
115520 BAA10g09870 A10 11717109 G A upstream_gene_variant MODIFIER c.-4448C>T| S261
115521 BAA10g09870 A10 11717569 C T upstream_gene_variant MODIFIER c.-4908G>A| S195
115522 BAA10g09880 A10 11719981 G A intron_variant MODIFIER c.925+100C>T| S89
115523 BAA10g09880 A10 11720311 C T missense_variant MODERATE c.695G>A|p.Gly232Glu S8
115524 BAA10g09880 A10 11720440 C T missense_variant MODERATE c.566G>A|p.Gly189Glu S133
115525 BAA10g09880 A10 11720545 G A missense_variant MODERATE c.461C>T|p.Ser154Phe S215
S59