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
103751 BAA10g07820 A10 4845319 C T synonymous_variant LOW c.198C>T|p.Thr66Thr S297
103752 BAA10g07820 A10 4846650 C T intron_variant MODIFIER c.462+1067C>T| S183
103753 BAA10g07820 A10 4847763 C T intron_variant MODIFIER c.463-86C>T| S124
103754 BAA10g07820 A10 4847797 C T intron_variant MODIFIER c.463-52C>T| S305
103755 BAA10g07820 A10 4848632 C T missense_variant MODERATE c.794C>T|p.Ser265Phe S259
103756 BAA10g07830 A10 4849313 G A downstream_gene_variant MODIFIER c.*3575C>T| S268
103757 BAA10g07820 A10 4851328 G A downstream_gene_variant MODIFIER c.*1340G>A| S25
103758 BAA10g07820 A10 4851556 G A downstream_gene_variant MODIFIER c.*1568G>A| S291
103759 BAA10g07820 A10 4852061 C T downstream_gene_variant MODIFIER c.*2073C>T| S40
S49
103760 BAA10g07820 A10 4852445 G A downstream_gene_variant MODIFIER c.*2457G>A| S53
103761 BAA10g07830 A10 4853034 G A missense_variant MODERATE c.1075C>T|p.Leu359Phe S198
103762 BAA10g07820 A10 4853310 C T downstream_gene_variant MODIFIER c.*3322C>T| S294
103763 BAA10g07830 A10 4853684 G A stop_gained HIGH c.862C>T|p.Gln288* S226
103764 BAA10g07830 A10 4854121 C T missense_variant&splice_region_variant MODERATE c.577G>A|p.Val193Ile S19
103765 BAA10g07830 A10 4854624 G A missense_variant MODERATE c.374C>T|p.Thr125Met S17
103766 BAA10g07830 A10 4854803 C T missense_variant MODERATE c.284G>A|p.Arg95Lys S40
S49
103767 BAA10g07830 A10 4855074 G A missense_variant MODERATE c.83C>T|p.Ala28Val S32
103768 BAA10g07830 A10 4857033 C T upstream_gene_variant MODIFIER c.-1877G>A| S23
103769 BAA10g07830 A10 4857749 C T upstream_gene_variant MODIFIER c.-2593G>A| S54
103770 BAA10g07830 A10 4859330 C T upstream_gene_variant MODIFIER c.-4174G>A| S84
S93
103771 BAA10g07830 A10 4859409 C T upstream_gene_variant MODIFIER c.-4253G>A| S235
103772 BAA10g07830 A10 4859523 C T upstream_gene_variant MODIFIER c.-4367G>A| S246
103773 BAA10g07830-BAA10g07840 A10 4860394 G A intergenic_region MODIFIER n.4860394G>A| S159
S243
S299
103774 BAA10g07830-BAA10g07840 A10 4862368 C T intergenic_region MODIFIER n.4862368C>T| S149
103775 BAA10g07830-BAA10g07840 A10 4863013 C T intergenic_region MODIFIER n.4863013C>T| S139