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
91201 BAA10g01170 A10 586343 C T missense_variant MODERATE c.591G>A|p.Met197Ile S297
91202 BAA10g01150 A10 586492 C T upstream_gene_variant MODIFIER c.-2643G>A| S104
91203 BAA10g01150 A10 586665 G A upstream_gene_variant MODIFIER c.-2816C>T| S1
S90
91204 BAA10g01150 A10 587296 C T upstream_gene_variant MODIFIER c.-3447G>A| S37
91205 BAA10g01170 A10 588079 C T missense_variant MODERATE c.163G>A|p.Glu55Lys S182
91206 BAA10g01150 A10 588461 G A upstream_gene_variant MODIFIER c.-4612C>T| S234
91207 BAA10g01170 A10 590797 G A upstream_gene_variant MODIFIER c.-2556C>T| S283
91208 BAA10g01170 A10 591669 G A upstream_gene_variant MODIFIER c.-3428C>T| S157
S163
91209 BAA10g01180 A10 596936 C T upstream_gene_variant MODIFIER c.-4199C>T| S67
91210 BAA10g01180 A10 597053 C T upstream_gene_variant MODIFIER c.-4082C>T| S176
91211 BAA10g01180 A10 597132 C T upstream_gene_variant MODIFIER c.-4003C>T| S205
91212 BAA10g01180 A10 598340 T C upstream_gene_variant MODIFIER c.-2795T>C| S290
91213 BAA10g01180 A10 599722 G A upstream_gene_variant MODIFIER c.-1413G>A| S53
91214 BAA10g01180 A10 601199 C T missense_variant MODERATE c.65C>T|p.Ser22Leu S42
91215 BAA10g01190 A10 601887 C T downstream_gene_variant MODIFIER c.*3170G>A| S68
91216 BAA10g01200 A10 604577 G A upstream_gene_variant MODIFIER c.-3797G>A| S156
91217 BAA10g01190 A10 605103 C T missense_variant MODERATE c.542G>A|p.Gly181Glu S75
91218 BAA10g01190 A10 606530 G A upstream_gene_variant MODIFIER c.-211C>T| S33
91219 BAA10g01190 A10 606969 C T upstream_gene_variant MODIFIER c.-650G>A| S202
91220 BAA10g01190 A10 607681 G A upstream_gene_variant MODIFIER c.-1362C>T| S198
91221 BAA10g01200 A10 609115 G A missense_variant MODERATE c.742G>A|p.Val248Ile S208
S219
91222 BAA10g01200 A10 609237 C T synonymous_variant LOW c.864C>T|p.Asp288Asp S162
S299
91223 BAA10g01210 A10 612758 C T upstream_gene_variant MODIFIER c.-539G>A| S183
91224 BAA10g01210 A10 613920 G A upstream_gene_variant MODIFIER c.-1701C>T| S148
S30
91225 BAA10g01210 A10 614296 C T upstream_gene_variant MODIFIER c.-2077G>A| S166