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
132601 BAA10g19450 A10 17830131 G A synonymous_variant LOW c.42C>T|p.Ser14Ser S272
132602 BAA10g19450 A10 17831016 C T upstream_gene_variant MODIFIER c.-844G>A| S174
S216
S241
S265
132603 BAA10g19450 A10 17831349 C T upstream_gene_variant MODIFIER c.-1177G>A| S92
132604 BAA10g19450 A10 17833237 C T upstream_gene_variant MODIFIER c.-3065G>A| S192
132605 BAA10g19450 A10 17833345 C T upstream_gene_variant MODIFIER c.-3173G>A| S236
132606 BAA10g19460 A10 17833816 C T missense_variant MODERATE c.202C>T|p.Pro68Ser S277
132607 BAA10g19460 A10 17834046 C T synonymous_variant LOW c.432C>T|p.Asn144Asn S11
132608 BAA10g19470 A10 17836215 G A upstream_gene_variant MODIFIER c.-1340G>A| S245
132609 BAA10g19470 A10 17836469 G A upstream_gene_variant MODIFIER c.-1086G>A| S240
132610 BAA10g19470 A10 17836534 C T upstream_gene_variant MODIFIER c.-1021C>T| S54
132611 BAA10g19470 A10 17837378 C T upstream_gene_variant MODIFIER c.-177C>T| S251
132612 BAA10g19470 A10 17837558 G A missense_variant MODERATE c.4G>A|p.Ala2Thr S207
132613 BAA10g19470 A10 17837681 C T missense_variant MODERATE c.127C>T|p.Pro43Ser S89
132614 BAA10g19470 A10 17839348 C T intron_variant MODIFIER c.735+257C>T| S246
132615 BAA10g19470 A10 17839847 C T intron_variant MODIFIER c.735+756C>T| S185
132616 BAA10g19480 A10 17841745 G A upstream_gene_variant MODIFIER c.-4452G>A| S111
132617 BAA10g19480 A10 17841767 C T upstream_gene_variant MODIFIER c.-4430C>T| S8
132618 BAA10g19480 A10 17841988 C T upstream_gene_variant MODIFIER c.-4209C>T| S170
132619 BAA10g19480 A10 17842031 G A upstream_gene_variant MODIFIER c.-4166G>A| S16
132620 BAA10g19480 A10 17842525 G A upstream_gene_variant MODIFIER c.-3672G>A| S85
132621 BAA10g19480 A10 17842807 C T upstream_gene_variant MODIFIER c.-3390C>T| S12
132622 BAA10g19480 A10 17842923 C T upstream_gene_variant MODIFIER c.-3274C>T| S148
S30
S31
132623 BAA10g19480 A10 17843385 G A upstream_gene_variant MODIFIER c.-2812G>A| S262
132624 BAA10g19480 A10 17844028 C T upstream_gene_variant MODIFIER c.-2169C>T| S161
132625 BAA10g19480 A10 17845374 G A upstream_gene_variant MODIFIER c.-823G>A| S4