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
146651 BAA10g31100 A10 22808939 G A synonymous_variant LOW c.1755C>T|p.Phe585Phe S203
146652 BAA10g31100 A10 22810289 C T missense_variant MODERATE c.580G>A|p.Glu194Lys S96
146653 BAA10g31110 A10 22810429 G A upstream_gene_variant MODIFIER c.-4134G>A| S228
146654 BAA10g31100 A10 22810904 G A synonymous_variant LOW c.228C>T|p.Ser76Ser S151
146655 BAA10g31100 A10 22812470 C T upstream_gene_variant MODIFIER c.-1339G>A| S142
146656 BAA10g31100 A10 22812578 G A upstream_gene_variant MODIFIER c.-1447C>T| S136
146657 BAA10g31110 A10 22814624 C T missense_variant MODERATE c.62C>T|p.Pro21Leu S112
146658 BAA10g31120 A10 22816954 C T upstream_gene_variant MODIFIER c.-746C>T| S5
146659 BAA10g31120 A10 22817053 G A upstream_gene_variant MODIFIER c.-647G>A| S191
146660 BAA10g31120 A10 22817637 G A upstream_gene_variant MODIFIER c.-63G>A| S240
146661 BAA10g31120 A10 22818098 C T synonymous_variant LOW c.399C>T|p.Thr133Thr S35
146662 BAA10g31130 A10 22818652 C T upstream_gene_variant MODIFIER c.-690C>T| S234
146663 BAA10g31130 A10 22818675 C T upstream_gene_variant MODIFIER c.-667C>T| S246
146664 BAA10g31130 A10 22819391 C T missense_variant MODERATE c.50C>T|p.Thr17Ile S187
146665 BAA10g31130 A10 22820261 C T missense_variant MODERATE c.736C>T|p.Leu246Phe S8
146666 BAA10g31130 A10 22820264 C T missense_variant MODERATE c.739C>T|p.Leu247Phe S238
146667 BAA10g31130 A10 22820931 G A synonymous_variant LOW c.1251G>A|p.Lys417Lys S66
146668 BAA10g31130 A10 22820973 A C splice_region_variant&intron_variant LOW c.1290+3A>C| S86
146669 BAA10g31130 A10 22821342 C T missense_variant MODERATE c.1490C>T|p.Ala497Val S20
146670 BAA10g31140 A10 22821637 C T upstream_gene_variant MODIFIER c.-532C>T| S295
146671 BAA10g31140 A10 22821887 G A upstream_gene_variant MODIFIER c.-282G>A| S86
146672 BAA10g31140 A10 22822201 C T synonymous_variant LOW c.33C>T|p.Ile11Ile S308
146673 BAA10g31120 A10 22822517 C T downstream_gene_variant MODIFIER c.*4151C>T| S286
146674 BAA10g31150 A10 22824096 C T missense_variant MODERATE c.2761G>A|p.Gly921Arg S36
146675 BAA10g31150 A10 22825980 G A synonymous_variant LOW c.877C>T|p.Leu293Leu S81