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
130751 BAA10g18270 A10 17167306 C T downstream_gene_variant MODIFIER c.*2143C>T| S45
130752 BAA10g18270 A10 17167663 C T downstream_gene_variant MODIFIER c.*2500C>T| S185
130753 BAA10g18270 A10 17168178 G A downstream_gene_variant MODIFIER c.*3015G>A| S120
130754 BAA10g18280 A10 17171560 G A downstream_gene_variant MODIFIER c.*1290C>T| S148
130755 BAA10g18280 A10 17171823 G A downstream_gene_variant MODIFIER c.*1027C>T| S298
130756 BAA10g18280 A10 17172063 C T downstream_gene_variant MODIFIER c.*787G>A| S48
130757 BAA10g18280 A10 17172083 C T downstream_gene_variant MODIFIER c.*767G>A| S96
130758 BAA10g18280 A10 17172150 G A downstream_gene_variant MODIFIER c.*700C>T| S132
S137
S215
130759 BAA10g18280 A10 17172531 G A downstream_gene_variant MODIFIER c.*319C>T| S262
130760 BAA10g18280 A10 17173195 G A synonymous_variant LOW c.2010C>T|p.Arg670Arg S1
S90
130761 BAA10g18280 A10 17173467 C T missense_variant MODERATE c.1816G>A|p.Val606Ile S210
130762 BAA10g18280 A10 17174389 C T synonymous_variant LOW c.1086G>A|p.Arg362Arg S44
130763 BAA10g18280 A10 17176094 G A missense_variant MODERATE c.182C>T|p.Pro61Leu S240
130764 BAA10g18280 A10 17176408 G A upstream_gene_variant MODIFIER c.-133C>T| S25
130765 BAA10g18280 A10 17178272 C T upstream_gene_variant MODIFIER c.-1997G>A| S306
S308
S78
130766 BAA10g18280 A10 17178345 C T upstream_gene_variant MODIFIER c.-2070G>A| S146
130767 BAA10g18280 A10 17178375 C T upstream_gene_variant MODIFIER c.-2100G>A| S20
130768 BAA10g18280 A10 17181032 A C upstream_gene_variant MODIFIER c.-4757T>G| S170
130769 BAA10g18300 A10 17181334 G A upstream_gene_variant MODIFIER c.-1717G>A| S209
130770 BAA10g18300 A10 17183228 G A missense_variant MODERATE c.178G>A|p.Gly60Arg S7
130771 BAA10g18290 A10 17185767 G A upstream_gene_variant MODIFIER c.-3532C>T| S42
130772 BAA10g18290 A10 17185934 C T upstream_gene_variant MODIFIER c.-3699G>A| S26
130773 BAA10g18290 A10 17186007 C T upstream_gene_variant MODIFIER c.-3772G>A| S238
130774 BAA10g18310 A10 17186703 G A missense_variant MODERATE c.54G>A|p.Met18Ile S212
130775 BAA10g18310 A10 17187022 G A missense_variant MODERATE c.373G>A|p.Asp125Asn S239