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
100201 BAA10g06860 A10 3683538 G A stop_gained HIGH c.1038G>A|p.Trp346* S259
100202 BAA10g06880 A10 3684035 C T upstream_gene_variant MODIFIER c.-2254C>T| S282
100203 BAA10g06880 A10 3685386 G A upstream_gene_variant MODIFIER c.-903G>A| S100
100204 BAA10g06870 A10 3685923 G A upstream_gene_variant MODIFIER c.-195C>T| S189
100205 BAA10g06880 A10 3686321 G A synonymous_variant LOW c.33G>A|p.Arg11Arg S12
100206 BAA10g06870 A10 3686443 C T upstream_gene_variant MODIFIER c.-715G>A| S259
100207 BAA10g06880 A10 3686631 C T missense_variant MODERATE c.245C>T|p.Pro82Leu S235
100208 BAA10g06880 A10 3686794 G A synonymous_variant LOW c.408G>A|p.Ala136Ala S86
100209 BAA10g06880 A10 3686940 G A missense_variant MODERATE c.461G>A|p.Cys154Tyr S276
100210 BAA10g06880 A10 3687336 C T missense_variant MODERATE c.857C>T|p.Thr286Ile S44
100211 BAA10g06880 A10 3687410 C T missense_variant MODERATE c.931C>T|p.Pro311Ser S79
S91
100212 BAA10g06880 A10 3687456 G A missense_variant MODERATE c.977G>A|p.Cys326Tyr S18
100213 BAA10g06880 A10 3687819 C T missense_variant MODERATE c.1250C>T|p.Pro417Leu S297
100214 BAA10g06880 A10 3687862 G A synonymous_variant LOW c.1293G>A|p.Ser431Ser S221
100215 BAA10g06880 A10 3688179 C T missense_variant MODERATE c.1610C>T|p.Ser537Phe S19
100216 BAA10g06870 A10 3688745 G A upstream_gene_variant MODIFIER c.-3017C>T| S151
S263
100217 BAA10g06880 A10 3689128 C T missense_variant MODERATE c.2060C>T|p.Ser687Phe S40
S49
100218 BAA10g06880 A10 3689255 G A synonymous_variant LOW c.2187G>A|p.Gly729Gly S57
100219 BAA10g06880 A10 3690179 G A missense_variant MODERATE c.2935G>A|p.Val979Ile S59
100220 BAA10g06880 A10 3690200 C T missense_variant MODERATE c.2956C>T|p.Pro986Ser S139
100221 BAA10g06880 A10 3690358 C T synonymous_variant LOW c.3114C>T|p.Ile1038Ile S235
100222 BAA10g06880 A10 3690450 G A splice_region_variant&intron_variant LOW c.3202+4G>A| S250
100223 BAA10g06900 A10 3690896 G A upstream_gene_variant MODIFIER c.-2431G>A| S53
100224 BAA10g06900 A10 3691097 C T upstream_gene_variant MODIFIER c.-2230C>T| S12
100225 BAA10g06900 A10 3691712 G A upstream_gene_variant MODIFIER c.-1615G>A| S50