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
142301 BAA10g27210 A10 21297921 C T missense_variant MODERATE c.232C>T|p.Pro78Ser S230
142302 BAA10g27210 A10 21298088 G A synonymous_variant LOW c.399G>A|p.Pro133Pro S179
142303 BAA10g27210 A10 21298170 G A missense_variant MODERATE c.481G>A|p.Ala161Thr S125
142304 BAA10g27210 A10 21298175 C T synonymous_variant LOW c.486C>T|p.Leu162Leu S283
142305 BAA10g27210 A10 21298959 C G downstream_gene_variant MODIFIER c.*355C>G| S226
142306 BAA10g27210 A10 21300001 G A downstream_gene_variant MODIFIER c.*1397G>A| S64
142307 BAA10g27210 A10 21300026 G A downstream_gene_variant MODIFIER c.*1422G>A| S132
S137
S215
142308 BAA10g27220 A10 21302188 C T missense_variant MODERATE c.2194G>A|p.Glu732Lys S38
142309 BAA10g27220 A10 21302737 C T missense_variant MODERATE c.1645G>A|p.Glu549Lys S47
142310 BAA10g27220 A10 21303069 G A missense_variant MODERATE c.1313C>T|p.Ser438Phe S9
142311 BAA10g27220 A10 21303454 C T missense_variant MODERATE c.928G>A|p.Glu310Lys S262
142312 BAA10g27220 A10 21303560 G A synonymous_variant LOW c.822C>T|p.Ala274Ala S279
142313 BAA10g27220 A10 21303770 C T synonymous_variant LOW c.612G>A|p.Leu204Leu S42
142314 BAA10g27220 A10 21303965 C T synonymous_variant LOW c.417G>A|p.Lys139Lys S11
142315 BAA10g27220 A10 21304672 C T upstream_gene_variant MODIFIER c.-291G>A| S68
142316 BAA10g27220 A10 21304696 C T upstream_gene_variant MODIFIER c.-315G>A| S37
142317 BAA10g27220 A10 21305074 C T upstream_gene_variant MODIFIER c.-693G>A| S167
142318 BAA10g27220 A10 21305626 G A upstream_gene_variant MODIFIER c.-1245C>T| S230
142319 BAA10g27220 A10 21305914 G A upstream_gene_variant MODIFIER c.-1533C>T| S128
142320 BAA10g27220 A10 21306143 G A upstream_gene_variant MODIFIER c.-1762C>T| S151
142321 BAA10g27220 A10 21306290 G A upstream_gene_variant MODIFIER c.-1909C>T| S151
142322 BAA10g27230 A10 21307270 G A missense_variant MODERATE c.2755C>T|p.Pro919Ser S286
142323 BAA10g27230 A10 21307672 C T missense_variant MODERATE c.2353G>A|p.Asp785Asn S210
142324 BAA10g27230 A10 21309352 G A missense_variant MODERATE c.1850C>T|p.Thr617Ile S118
142325 BAA10g27230 A10 21309704 C T splice_donor_variant&intron_variant HIGH c.1728+1G>A| S282