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
92001 BAA10g01830 A10 883904 G A missense_variant MODERATE c.199G>A|p.Asp67Asn S250
92002 BAA10g01830 A10 884223 G A missense_variant MODERATE c.215G>A|p.Gly72Glu S251
92003 BAA10g01840 A10 884985 G A upstream_gene_variant MODIFIER c.-1966G>A| S148
S30
92004 BAA10g01840 A10 885811 G A upstream_gene_variant MODIFIER c.-1140G>A| S65
92005 BAA10g01840 A10 886395 G A upstream_gene_variant MODIFIER c.-556G>A| S234
92006 BAA10g01840 A10 887361 C T missense_variant MODERATE c.334C>T|p.Leu112Phe S131
92007 BAA10g01830 A10 887613 A G downstream_gene_variant MODIFIER c.*2775A>G| S231
92008 BAA10g01840 A10 887707 G A missense_variant MODERATE c.409G>A|p.Val137Ile S236
92009 BAA10g01850 A10 892145 G A missense_variant MODERATE c.3250C>T|p.Leu1084Phe S242
92010 BAA10g01850 A10 892372 G A missense_variant MODERATE c.3023C>T|p.Ser1008Phe S140
92011 BAA10g01850 A10 893256 C T synonymous_variant LOW c.2139G>A|p.Glu713Glu S44
92012 BAA10g01850 A10 893393 G A synonymous_variant LOW c.2002C>T|p.Leu668Leu S171
92013 BAA10g01850 A10 893737 G A missense_variant MODERATE c.1658C>T|p.Ala553Val S256
92014 BAA10g01850 A10 893781 G A synonymous_variant LOW c.1614C>T|p.Ala538Ala S47
92015 BAA10g01850 A10 895031 C T missense_variant MODERATE c.364G>A|p.Glu122Lys S263
92016 BAA10g01850 A10 895430 C T missense_variant MODERATE c.53G>A|p.Ser18Asn S116
92017 BAA10g01850 A10 895534 G A upstream_gene_variant MODIFIER c.-52C>T| S1
S90
92018 BAA10g01850 A10 895546 G A upstream_gene_variant MODIFIER c.-64C>T| S79
S84
92019 BAA10g01850 A10 896043 G A upstream_gene_variant MODIFIER c.-561C>T| S64
92020 BAA10g01850 A10 897050 C T upstream_gene_variant MODIFIER c.-1568G>A| S131
92021 BAA10g01850 A10 897146 C T upstream_gene_variant MODIFIER c.-1664G>A| S288
92022 BAA10g01850 A10 897700 C T upstream_gene_variant MODIFIER c.-2218G>A| S225
92023 BAA10g01850 A10 898440 C T upstream_gene_variant MODIFIER c.-2958G>A| S176
92024 BAA10g01880 A10 898981 C T missense_variant MODERATE c.2309G>A|p.Gly770Glu S79
S91
92025 BAA10g01880 A10 899209 G A missense_variant MODERATE c.2081C>T|p.Thr694Ile S158